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The molecule is a positive allosteric modulator, a npy y5 antagonist, and a kinase inhibitor, belonging to both the diabetes treatment and anti obesity classes, and is gpr119 modulator.
CC(=N)C1CCC(C)CC1
[ "diabetes treatment", "positive allosteric modulator", "anti obesity", "gpr119 modulator", "npy y5 antagonist", "kinase inhibitor" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a nutrient.
CCCCC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CCC(=O)OC[C@H](COP(=O)(O)OC[C@H](N)C(=O)O)OC(=O)CC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CCCCC
[ "nutrient" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a stabilizing mitochondrial structure, cholesterol translocation, stabilizing cytochrome oxidase, apoptosis that impacts aging. The molecule is a proton trap for oxidative phosphorylation that impacts barth syndrome, tangier disease, non-alcoholic fatty liver disease, and diabetic heart disease.
CCCCCCCCCCCCCCCCCCCCCCC(=O)O[C@H](COC(=O)CCCCCCCCCCCC)COP(=O)(O)OC[C@@H](O)COP(=O)(O)OC[C@@H](COC(=O)CCCCCCCCC(C)C)OC(=O)CCCCCCCCC(C)C
[ "Stabilizing mitochondrial structure", "Aging", "Cholesterol translocation", "Stabilizing cytochrome oxidase", "Apoptosis", "Proton trap for oxidative phosphorylation", "Barth syndrome", "Tangier disease", "Non-alcoholic fatty liver disease", "Diabetic heart disease" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a fat storage and belongs to the thyroxine treatment class of molecules, impacting metabolic syndrome. The molecule is a nutrient that impacts cardiovascular disease, atherosclerosis, and pancreatitis.
CC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)OC[C@H](COC(=O)CCCC/C=C\C/C=C\C/C=C\C/C=C\CC)OC(=O)CCCCCCCCCCC/C=C\CCCCCCCC
[ "Thyroxine treatment", "Metabolic syndrome", "Fat storage", "Cardiovascular disease", "Atherosclerosis", "nutrient", "Pancreatitis" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
It belongs to the anti bacterial class of molecules.
N#CCc1c(F)cc(Br)c([N+](=O)[O-])c1F
[ "anti bacterial" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a energy source, membrane stabilizer, nutrient, energy storage that impacts cancer and atherosclerosis. The molecule is a inflammatory that impacts both metabolic syndrome and pancreatitis. The molecule is a fat storage and a thyroxine treatment, impacting both cardiovascular disease and obesity.
CCC(C)CCCCCCCCC(=O)O[C@@H](COC(=O)CCCCCCCCCCCCCCCCCCCCC(C)C)COC(=O)CCCCCCCCCCCCCCC(C)C
[ "Energy source", "Cancer", "Membrane stabilizer", "Atherosclerosis", "nutrient", "Energy storage", "inflammatory", "Metabolic syndrome", "Pancreatitis", "Cardiovascular disease", "Obesity", "Fat storage", "Thyroxine treatment" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a inflammatory that impacts obesity, cancer, cardiovascular disease, pancreatitis, and metabolic syndrome. The molecule is a nutrient, a membrane stabilizer, and a energy storage. The molecule is a fat storage and a energy source, impacting both atherosclerosis and thyroxine treatment.
CCCCCCCCCCCCCCCCCCCC(=O)O[C@H](COC(=O)CCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCC(C)C
[ "Obesity", "Cancer", "inflammatory", "Cardiovascular disease", "Pancreatitis", "Metabolic syndrome", "nutrient", "Membrane stabilizer", "Energy storage", "Fat storage", "Energy source", "Atherosclerosis", "Thyroxine treatment" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a hiv protease inhibitor.
CNCc1cc(OC)c(OC)cc1-c1sc2c(c1C(=O)O)CC(C)(C)CC2
[ "hiv protease inhibitor" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a emulsifier and a energy source, impacting both barth syndrome and non-alcoholic fatty liver disease. The molecule is a cholesterol translocation, membrane stabilizer, energy storage, food additive, proton trap for oxidative phosphorylation. The molecule is a stabilizing cytochrome oxidase, a nutrition...
CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)O[C@H](COC(=O)CCCCCCC/C=C\CCCCCCCC)COP(=O)(O)OC[C@H](O)COP(=O)(O)OC[C@@H](COC(=O)CCCCCCC/C=C\C=C/CCCCCC)OC(=O)CCCCCCC/C=C\CCCCCCCC
[ "Barth syndrome", "Emulsifier", "Energy source", "Non-alcoholic fatty liver disease", "Cholesterol translocation", "Membrane stabilizer", "Energy storage", "food additive", "Proton trap for oxidative phosphorylation", "Stabilizing cytochrome oxidase", "Nutritional supplement", "Stabilizing mit...
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a diabetes treatment and is anti diabetic.
Cc1cc2c(cn1)c(=O)cc(S(=O)CC1CCCCC1)n2-c1ccccc1
[ "anti diabetic", "diabetes treatment" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a inflammation treatment member of the cancer treatment class.
CC1C=Cc2oc3nc(=O)[nH]c(=O)c-3cc2C1
[ "inflammation treatment", "cancer treatment" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a anti viral, hcv treatment, and anti viral activity compound.
CNC(=O)c1c(-c2ccc(F)cc2)oc2ccc(-c3cc(C(=O)N(c4ccccn4)C4CC4)c(OCC(N)=O)cc3C)cc12
[ "anti viral", "hcv treatment", "anti viral activity" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a cholesterol translocation and a stabilizing mitochondrial structure that impacts barth syndrome, aging, and non-alcoholic fatty liver disease. The molecule is a stabilizing cytochrome oxidase, proton trap for oxidative phosphorylation, apoptosis that impacts tangier disease and diabetic heart disease.
CC/C=C\C/C=C\C/C=C\C/C=C\CCCCC(=O)OC[C@H](COP(=O)(O)OC[C@H](O)COP(=O)(O)OC[C@@H](COC(=O)CC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CCCCC)OC(=O)CCCCCCC/C=C\C/C=C\CCCCC)OC(=O)CCCCCCC/C=C\C/C=C\CCCCC
[ "Cholesterol translocation", "Stabilizing mitochondrial structure", "Barth syndrome", "Aging", "Non-alcoholic fatty liver disease", "Tangier disease", "Stabilizing cytochrome oxidase", "Proton trap for oxidative phosphorylation", "Diabetic heart disease", "Apoptosis" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule has Odorless. When heated to decomposition it emits acrid smoke and irritating fumes.
C=C(C)C1Cc2c(ccc3c2OC2COc4cc(OC)c(OC)cc4C2C3=O)O1
[ "Odor_evaluation", "Decomposition_evaluation" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a stabilizing cytochrome oxidase, stabilizing mitochondrial structure, apoptosis that impacts diabetic heart disease and barth syndrome. The molecule is a proton trap for oxidative phosphorylation and a cholesterol translocation that impacts non-alcoholic fatty liver disease, tangier disease, and aging.
CC/C=C\C/C=C\C/C=C\CCCCCCCCCC(=O)O[C@H](COC(=O)CC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CCCCC)COP(=O)(O)OC[C@@H](O)COP(=O)(O)OC[C@@H](COC(=O)CCCCCCCCCCCCCCC)OC(=O)CCCCCCC/C=C\CCCCCC
[ "Diabetic heart disease", "Stabilizing cytochrome oxidase", "Barth syndrome", "Stabilizing mitochondrial structure", "Apoptosis", "Non-alcoholic fatty liver disease", "Tangier disease", "Aging", "Proton trap for oxidative phosphorylation", "Cholesterol translocation" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is inflammation treatment.
CCOC(=O)CCc1cc(-c2ccccc2)ccc1OCCCOc1cc(O)c(C(C)=O)cc1CC
[ "inflammation treatment" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a nutrient that impacts parkinson's disease, non-alcoholic fatty liver disease, alzheimer's disease, and diabetes mellitus type 2.
CCCCCC/C=C\CCCCCCCCCC(=O)OC[C@H](COP(=O)(O)OCCN)OC(=O)CCC/C=C\C/C=C\C/C=C\C=C\[C@@H](O)CCCCC
[ "Parkinson's disease", "Non-alcoholic fatty liver disease", "Alzheimer's Disease", "Diabetes mellitus type 2", "nutrient" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a apoptosis, stabilizing cytochrome oxidase, stabilizing mitochondrial structure that impacts barth syndrome and diabetic heart disease. The molecule is a cholesterol translocation and a proton trap for oxidative phosphorylation that impacts aging, non-alcoholic fatty liver disease, and tangier disease.
CCCCCCCCCCCCCCCCCCCCC(=O)O[C@H](COC(=O)CCCCCCCCCCCCCCCC(C)C)COP(=O)(O)OC[C@@H](O)COP(=O)(O)OC[C@@H](COC(=O)CCCCCCCCCC(C)C)OC(=O)CCCCCCCCCCCCCCCC
[ "Apoptosis", "Stabilizing cytochrome oxidase", "Barth syndrome", "Diabetic heart disease", "Stabilizing mitochondrial structure", "Aging", "Cholesterol translocation", "Proton trap for oxidative phosphorylation", "Non-alcoholic fatty liver disease", "Tangier disease" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a fat storage and nutrient, and it impacts thyroxine treatment. It impacts metabolic syndrome, atherosclerosis, cardiovascular disease, and pancreatitis.
CC/C=C\C/C=C\C/C=C\C/C=C\CCCCC(=O)OC[C@@H](COCCCCCCCCCCCCCCCCCC)OC(=O)CCCCCCC/C=C\CCCCCC
[ "Fat storage", "Thyroxine treatment", "nutrient", "Metabolic syndrome", "Atherosclerosis", "Cardiovascular disease", "Pancreatitis" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a nutrient.
CC/C=C\C/C=C\C/C=C\C/C=C\C=C/C(O)C/C=C\CCC(=O)O[C@H](COC(=O)CCC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CC)COP(=O)(O)OC[C@H](N)C(=O)O
[ "nutrient" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a kinase inhibitor and is cancer treatment.
CC1CC(NC(=O)OC(C)(C)C)CC(c2ccncc2NC(=O)c2ccc(F)c(-c3c(F)ccc(C=O)c3F)n2)C1
[ "kinase inhibitor", "cancer treatment" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
When heated to decomposition it emits very toxic fumes of chlorides, nitrogen oxides, and cyanides. The molecule has Pungent odor.
N#CCCl
[ "Decomposition_evaluation", "Odor_evaluation" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a membrane stabilizer, energy source, fat storage, inflammatory that has an effect on cancer and impacts cardiovascular disease. The molecule is a nutrient and thyroxine treatment, and it impacts atherosclerosis. The molecule is a energy storage that impacts obesity, pancreatitis, and metabolic syndrome...
CCCCCCCCCCCC(=O)O[C@H](COC(=O)CCCCCCCCC)COC(=O)CCCCCCCCCCCCC(C)C
[ "Membrane stabilizer", "Cardiovascular disease", "Cancer", "Energy source", "Fat storage", "inflammatory", "Thyroxine treatment", "nutrient", "Atherosclerosis", "Obesity", "Pancreatitis", "Energy storage", "Metabolic syndrome" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is anti hypertensive.
CC1(C)C=C(n2cc(Br)cc([N+](=O)[O-])c2=O)c2cccnc2O1
[ "anti hypertensive" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is diabetes treatment.
CCCCOc1ccc(CC(N)C2=NC(C=C(C)C=C(C)C(=O)OCC)CS2)cc1
[ "diabetes treatment" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a stabilizing mitochondrial structure, stabilizing cytochrome oxidase, proton trap for oxidative phosphorylation that impacts non-alcoholic fatty liver disease and diabetic heart disease. The molecule is a cholesterol translocation and a apoptosis that impacts tangier disease, aging, and barth syndrome.
CCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)(O)OC[C@H](O)COP(=O)(O)OC[C@@H](COC(=O)CCCCCCCCCCCCCCCCC(C)C)OC(=O)CCCCCCCCCCCCCCCCCCCCC(C)C)OC(=O)CCCCCCCCCCCCCCCCC(C)C
[ "Stabilizing mitochondrial structure", "Non-alcoholic fatty liver disease", "Stabilizing cytochrome oxidase", "Proton trap for oxidative phosphorylation", "Diabetic heart disease", "Tangier disease", "Aging", "Cholesterol translocation", "Apoptosis", "Barth syndrome" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a nutrient that impacts both metabolic syndrome and atherosclerosis. The molecule is a fat storage and belongs to the thyroxine treatment class of molecules, impacting both cardiovascular disease and pancreatitis.
CCCCC/C=C\C/C=C\C/C=C\CCCCCCC(=O)O[C@H](COC(=O)CCCC/C=C\C/C=C\C/C=C\CCCCC)COC(=O)CCCCCCC/C=C\C/C=C\CCCCC
[ "Metabolic syndrome", "Atherosclerosis", "nutrient", "Fat storage", "Cardiovascular disease", "Thyroxine treatment", "Pancreatitis" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a fat storage, energy storage, nutrient, membrane stabilizer that has an effect on cancer and impacts atherosclerosis. It impacts obesity, metabolic syndrome, and pancreatitis. The molecule is a inflammatory and energy source, belonging to the thyroxine treatment class of molecules, and impacts cardiova...
CCCCCCCCCCCCCCC(=O)O[C@H](COC(=O)CCCCCCCCCCCCCCCCCC(C)C)COC(=O)CCCCCCCCC(C)CC
[ "Fat storage", "Energy storage", "nutrient", "Cancer", "Membrane stabilizer", "Atherosclerosis", "Obesity", "Metabolic syndrome", "Pancreatitis", "inflammatory", "Thyroxine treatment", "Energy source", "Cardiovascular disease" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a nutrient that impacts both cardiovascular disease and metabolic syndrome. The molecule is a fat storage and thyroxine treatment, impacting both pancreatitis and atherosclerosis.
CCCCCCCC/C=C\CCCCCCCCCC(=O)O[C@@H](COC(=O)CCCCCCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCCCCCCCC
[ "Cardiovascular disease", "Metabolic syndrome", "nutrient", "Pancreatitis", "Fat storage", "Thyroxine treatment", "Atherosclerosis" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
It impacts thyroxine treatment, cardiovascular disease, and metabolic syndrome. The molecule is a nutrient and a fat storage, impacting both atherosclerosis and pancreatitis.
CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)OC[C@H](COC(=O)CCCCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCC/C=C\CCCCCCCC
[ "Thyroxine treatment", "Cardiovascular disease", "Metabolic syndrome", "Atherosclerosis", "nutrient", "Fat storage", "Pancreatitis" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a cholesterol translocation, proton trap for oxidative phosphorylation, apoptosis, stabilizing mitochondrial structure that impacts non-alcoholic fatty liver disease. The molecule is a stabilizing cytochrome oxidase that impacts tangier disease, diabetic heart disease, aging, and barth syndrome.
CC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CCCCCC(=O)OC[C@H](COP(=O)(O)OC[C@@H](O)COP(=O)(O)OC[C@@H](COC(=O)CCC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CC)OC(=O)CCCCCCCCC/C=C\C/C=C\CCCCC)OC(=O)CCC/C=C\C/C=C\C/C=C\C/C=C\CCCCC
[ "Cholesterol translocation", "Proton trap for oxidative phosphorylation", "Apoptosis", "Stabilizing mitochondrial structure", "Non-alcoholic fatty liver disease", "Tangier disease", "Diabetic heart disease", "Stabilizing cytochrome oxidase", "Aging", "Barth syndrome" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a stabilizing cytochrome oxidase, stabilizing mitochondrial structure, proton trap for oxidative phosphorylation, apoptosis that impacts diabetic heart disease. The molecule is a cholesterol translocation that impacts barth syndrome, non-alcoholic fatty liver disease, aging, and tangier disease.
CC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)O[C@H](COC(=O)CCCCCCC/C=C\C/C=C\CCCCC)COP(=O)(O)OC[C@H](O)COP(=O)(O)OC[C@@H](COC(=O)CCCCCCCCC/C=C\C/C=C\C/C=C\CC)OC(=O)CCC/C=C\C/C=C\C/C=C\C/C=C\CCCCC
[ "Stabilizing cytochrome oxidase", "Stabilizing mitochondrial structure", "Proton trap for oxidative phosphorylation", "Diabetic heart disease", "Apoptosis", "Barth syndrome", "Cholesterol translocation", "Non-alcoholic fatty liver disease", "Aging", "Tangier disease" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is cancer treatment.
CN(C)C1CCN(c2ccc3c(c2)CC(CN)(c2cccc(-c4ncnc5[nH]ccc45)c2)C3)C1
[ "cancer treatment" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a immunomodulator and belongs to both the cb2 agonist and inflammation treatment classes of molecules.
CC(C)(C)c1cc(NC(=O)C(C)(C)S(=O)(=O)c2ccc(C(F)(F)F)nc2)n[nH]1
[ "cb2 agonist", "immunomodulator", "inflammation treatment" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a proton trap for oxidative phosphorylation and a apoptosis that impacts aging, non-alcoholic fatty liver disease, and tangier disease. The molecule is a cholesterol translocation, stabilizing mitochondrial structure, stabilizing cytochrome oxidase that impacts barth syndrome and diabetic heart disease.
CC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CCCCCC(=O)O[C@H](COC(=O)CCCCCCCCCCCCCCC)COP(=O)(O)OC[C@H](O)COP(=O)(O)OC[C@@H](COC(=O)CCCCCCC/C=C\CCCCCC)OC(=O)CCC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CC
[ "Aging", "Non-alcoholic fatty liver disease", "Proton trap for oxidative phosphorylation", "Apoptosis", "Tangier disease", "Cholesterol translocation", "Stabilizing mitochondrial structure", "Barth syndrome", "Diabetic heart disease", "Stabilizing cytochrome oxidase" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a cholesterol translocation, apoptosis, food additive, proton trap for oxidative phosphorylation. The molecule is a emulsifier, energy source, stabilizing cytochrome oxidase that impacts non-alcoholic fatty liver disease and barth syndrome. The molecule is a stabilizing mitochondrial structure and smoot...
CCC(C)CCCCCCCCCCCCCCCCCCCCC(=O)O[C@H](COC(=O)CCCCCCCCCC(C)C)COP(=O)(O)OC[C@@H](O)COP(=O)(O)OC[C@@H](COC(=O)CCCCCCCCC(C)CC)OC(=O)CCCCCCCCCCCCCCCCC(C)CC
[ "Cholesterol translocation", "Apoptosis", "food additive", "Proton trap for oxidative phosphorylation", "Non-alcoholic fatty liver disease", "Barth syndrome", "Emulsifier", "Energy source", "Stabilizing cytochrome oxidase", "Smooth", "Stabilizing mitochondrial structure", "Aging", "Tangier d...
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a pim kinase inhibitor, a kinase inhibitor, and cancer treatment.
CC(C)(C)OC(=O)NC1CCCN(c2ccccc2[N+](=O)[O-])C1.O=C1C2=CC=C1C=C2
[ "cancer treatment", "pim kinase inhibitor", "kinase inhibitor" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a fat storage, energy source, inflammatory, energy storage that impacts cancer and atherosclerosis. The molecule is a nutrient that impacts both pancreatitis and metabolic syndrome. The molecule is a membrane stabilizer and thyroxine treatment, impacting both obesity and cardiovascular disease.
CC(C)CCCCCCCCCCCCCCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCCCCCCCCCC(C)C)OC(=O)CCCCCCCCCCCC(C)C
[ "Fat storage", "Energy source", "Cancer", "inflammatory", "Atherosclerosis", "Energy storage", "Pancreatitis", "Metabolic syndrome", "nutrient", "Membrane stabilizer", "Obesity", "Cardiovascular disease", "Thyroxine treatment" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a stabilizing mitochondrial structure, proton trap for oxidative phosphorylation, stabilizing cytochrome oxidase, cholesterol translocation that impacts aging. The molecule is a apoptosis that impacts barth syndrome, tangier disease, diabetic heart disease, and non-alcoholic fatty liver disease.
CC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CCC(=O)O[C@H](COC(=O)CCCCCCC/C=C\CCCCCCCC)COP(=O)(O)OC[C@@H](O)COP(=O)(O)OC[C@@H](COC(=O)CCCCCCCCCCCCC)OC(=O)CC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CC
[ "Stabilizing mitochondrial structure", "Proton trap for oxidative phosphorylation", "Stabilizing cytochrome oxidase", "Aging", "Cholesterol translocation", "Apoptosis", "Barth syndrome", "Tangier disease", "Diabetic heart disease", "Non-alcoholic fatty liver disease" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
It belongs to the anti retroviral class of molecules.
CC(C)C(NC(=O)OC(C)C1CCCCN1)C(=O)O
[ "anti retroviral" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a fat storage and nutrient, and it impacts atherosclerosis. It impacts cardiovascular disease, thyroxine treatment, pancreatitis, and metabolic syndrome.
CC/C=C\C/C=C\C/C=C\C/C=C\CCCCC(=O)OC[C@H](COC(=O)CCCCCCCCCCC/C=C\CCCCCCCC)OC(=O)CCCCCCCCCCCCCC
[ "Fat storage", "Atherosclerosis", "nutrient", "Cardiovascular disease", "Thyroxine treatment", "Pancreatitis", "Metabolic syndrome" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
It impacts diabetes treatment.
CCCCCS(=O)(=O)NC(=O)C=Cc1c(Cl)nc(C)n1Cc1ccc(Cl)cc1Cl
[ "diabetes treatment" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a stabilizing mitochondrial structure, cholesterol translocation, proton trap for oxidative phosphorylation, apoptosis that impacts barth syndrome. The molecule is a stabilizing cytochrome oxidase that impacts diabetic heart disease, non-alcoholic fatty liver disease, tangier disease, and aging.
CC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CCCCCC(=O)O[C@H](COC(=O)CCCCCCC/C=C\C/C=C\CCCCC)COP(=O)(O)OC[C@H](O)COP(=O)(O)OC[C@@H](COC(=O)CCCCCCCCCCCCC)OC(=O)CCCCC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CC
[ "Barth syndrome", "Stabilizing mitochondrial structure", "Cholesterol translocation", "Proton trap for oxidative phosphorylation", "Apoptosis", "Diabetic heart disease", "Non-alcoholic fatty liver disease", "Tangier disease", "Aging", "Stabilizing cytochrome oxidase" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a cholesterol translocation, proton trap for oxidative phosphorylation, apoptosis that impacts diabetic heart disease and non-alcoholic fatty liver disease. The molecule is a stabilizing cytochrome oxidase and a stabilizing mitochondrial structure that impacts barth syndrome, aging, and tangier disease.
CCC(C)CCCCCCCCCCC(=O)OC[C@H](COP(=O)(O)OC[C@@H](O)COP(=O)(O)OC[C@@H](COC(=O)CCCCCCCCCCC(C)CC)OC(=O)CCCCCCCCCCC(C)CC)OC(=O)CCCCCCCCCCCCC(C)C
[ "Cholesterol translocation", "Diabetic heart disease", "Proton trap for oxidative phosphorylation", "Non-alcoholic fatty liver disease", "Apoptosis", "Barth syndrome", "Aging", "Stabilizing cytochrome oxidase", "Tangier disease", "Stabilizing mitochondrial structure" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a proton trap for oxidative phosphorylation, stabilizing mitochondrial structure, stabilizing cytochrome oxidase that impacts non-alcoholic fatty liver disease and diabetic heart disease. The molecule is a cholesterol translocation and a apoptosis that impacts barth syndrome, aging, and tangier disease.
CCCCC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CCC(=O)O[C@H](COC(=O)CCCCCCCCCCCCCCCCC)COP(=O)(O)OC[C@@H](O)COP(=O)(O)OC[C@@H](COC(=O)CCCCCCCCCCCCCCCCC)OC(=O)CCCCCCC/C=C\CCCCCCCC
[ "Proton trap for oxidative phosphorylation", "Stabilizing mitochondrial structure", "Stabilizing cytochrome oxidase", "Non-alcoholic fatty liver disease", "Diabetic heart disease", "Barth syndrome", "Aging", "Tangier disease", "Cholesterol translocation", "Apoptosis" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a apoptosis, stabilizing mitochondrial structure, cholesterol translocation that impacts barth syndrome and tangier disease. The molecule is a stabilizing cytochrome oxidase and a proton trap for oxidative phosphorylation that impacts aging, diabetic heart disease, and non-alcoholic fatty liver disease.
CC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CCC(=O)OC[C@H](COP(=O)(O)OC[C@H](O)COP(=O)(O)OC[C@@H](COC(=O)CCCCCCCCCCCCCCC)OC(=O)CCCCCCC/C=C\CCCCCCCC)OC(=O)CC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CCCCC
[ "Apoptosis", "Barth syndrome", "Tangier disease", "Stabilizing mitochondrial structure", "Cholesterol translocation", "Aging", "Stabilizing cytochrome oxidase", "Diabetic heart disease", "Non-alcoholic fatty liver disease", "Proton trap for oxidative phosphorylation" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a energy source, signalling molecule, surfactant, membrane stabilizer, emulsifier, energy storage.
CC(=O)c1ccc(C)cc1C
[ "Energy source", "signalling molecule", "surfactant", "Membrane stabilizer", "Emulsifier", "Energy storage" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a bace1 inhibitor and belongs to the alzheimer's treatment class of molecules.
CN=S1(=O)CC(C)(c2cc(-c3cc(-c4cnc(OC)cn4)no3)ccc2F)N=C(NC(=O)O)C1(C)C
[ "alzheimer's treatment", "bace1 inhibitor" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is anti bacterial.
NC1CCCC1SC1OC(CO)C(O)C(O)C1O
[ "anti bacterial" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a anti depressant.
Cc1ccc2c(c1)C1CC(O)C3CCCCC3N1CC2
[ "anti depressant" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a nutrient that affects both breast cancer and cervical cancer, and also impacts atherosclerosis and ulcerative colitis.
CC/C=C\C/C=C\C/C=C\C/C=C\CCCCC(=O)OC[C@H](COP(=O)([O-])OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCC/C=C\CCCCCCCC
[ "Atherosclerosis", "nutrient", "Ulcerative colitis", "Breast cancer", "Cervical cancer" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
It impacts insulin resistance.
CC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CCCCCC(=O)OC[C@H](O)COC(=O)CCCCCCCCCCCCCCCCCCC
[ "Insulin resistance" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a nutrient that impacts cervical cancer, atherosclerosis, ulcerative colitis, and breast cancer.
CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](COC(=O)CCCCCC[C@H]1[C@@H](O)CC(=O)[C@@H]1/C=C/[C@@H](O)CCCCC)COP(=O)([O-])OCC[N+](C)(C)C
[ "Cervical cancer", "Atherosclerosis", "nutrient", "Ulcerative colitis", "Breast cancer" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a nutrient.
CC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CCC(=O)O[C@H](COC(=O)CCC/C=C\C[C@H]1C(=O)C[C@@H](O)[C@@H]1/C=C/[C@@H](O)CCCCC)COP(=O)(O)OC[C@H](N)C(=O)O
[ "nutrient" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a nutrient that impacts parkinson's disease, non-alcoholic fatty liver disease, diabetes mellitus type 2, and alzheimer's disease.
CC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CCC(=O)OC[C@H](COP(=O)(O)OCCN)OC(=O)CCC/C=C/C/C=C\C[C@@H](O)/C=C\C=C/CCCCC
[ "Parkinson's disease", "nutrient", "Non-alcoholic fatty liver disease", "Diabetes mellitus type 2", "Alzheimer's Disease" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is cancer treatment.
CNC(=O)c1ccc(Nc2ncnc3cc(OC)c(NC(=O)C4CCCN4C(=O)C(NCC(C)NC)C(C)(C)C)cc23)cc1
[ "cancer treatment" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a cholesterol translocation, stabilizing cytochrome oxidase, stabilizing mitochondrial structure that impacts diabetic heart disease and tangier disease. The molecule is a apoptosis and a proton trap for oxidative phosphorylation that impacts non-alcoholic fatty liver disease, aging, and barth syndrome.
CCCCCC/C=C\C=C/CCCCCCCC(=O)OC[C@H](COP(=O)(O)OC[C@@H](O)COP(=O)(O)OC[C@@H](COC(=O)CCCCCCCCCC(C)C)OC(=O)CCCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCCCCCCC
[ "Diabetic heart disease", "Cholesterol translocation", "Stabilizing cytochrome oxidase", "Stabilizing mitochondrial structure", "Tangier disease", "Non-alcoholic fatty liver disease", "Apoptosis", "Aging", "Proton trap for oxidative phosphorylation", "Barth syndrome" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a thyroxine treatment that impacts both pancreatitis and atherosclerosis. The molecule is a fat storage and a nutrient, impacting both metabolic syndrome and cardiovascular disease.
CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)OCC(COC(=O)CCC/C=C\C/C=C\C/C=C\C/C=C\CCCCC)OC(=O)CCCCCCCCCCCCCCCCCCC
[ "Pancreatitis", "Thyroxine treatment", "Atherosclerosis", "Fat storage", "Metabolic syndrome", "Cardiovascular disease", "nutrient" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is both a fluorescent and a fluorescent dye.
CCCC[N+]1=C(C=CC=C2N(CCCS(=O)(=O)O)c3ccc4ccc(S(=O)(=O)O)cc4c3C2(C)CCCS(=O)(=O)O)C(C)(C)c2c1ccc1c(S(=O)(=O)O)cc(S(=O)(=O)O)cc21
[ "fluorescent", "fluorescent dye" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a stabilizing cytochrome oxidase and a apoptosis that impacts non-alcoholic fatty liver disease, barth syndrome, and aging. The molecule is a proton trap for oxidative phosphorylation, stabilizing mitochondrial structure, cholesterol translocation that impacts tangier disease and diabetic heart disease.
CCCCCCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)(O)OC[C@@H](O)COP(=O)(O)OC[C@@H](COC(=O)CCCCCCCCC(C)C)OC(=O)CCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCCCC
[ "Non-alcoholic fatty liver disease", "Barth syndrome", "Stabilizing cytochrome oxidase", "Apoptosis", "Aging", "Proton trap for oxidative phosphorylation", "Tangier disease", "Stabilizing mitochondrial structure", "Diabetic heart disease", "Cholesterol translocation" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is obesity treatment and it impacts diabetes treatment.
O=C1CCC(C=C(c2ccc(S(=O)(=O)C3CC3)cc2)c2ccc(C(F)(F)F)c(=O)[nH]2)C1
[ "obesity treatment", "diabetes treatment" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a nutrient and fat storage, and it impacts metabolic syndrome. It impacts thyroxine treatment, atherosclerosis, cardiovascular disease, and pancreatitis.
CC/C=C\C/C=C\C/C=C\C/C=C\CCCCCCC(=O)OC[C@H](COC(=O)CCCC/C=C\C/C=C\C/C=C\CCCCC)OC(=O)CCCCCCC/C=C\C/C=C\CCCCC
[ "Metabolic syndrome", "nutrient", "Fat storage", "Thyroxine treatment", "Atherosclerosis", "Cardiovascular disease", "Pancreatitis" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a member of the thyroxine treatment class and affects both atherosclerosis and pancreatitis. The molecule is a nutrient and a fat storage, impacting both metabolic syndrome and cardiovascular disease.
CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)O[C@H](COC(=O)CCCCCCCCCCC/C=C\C/C=C\CCCCC)COC(=O)CCCCCCCCCCCCCCCCC
[ "Atherosclerosis", "Pancreatitis", "Thyroxine treatment", "nutrient", "Fat storage", "Metabolic syndrome", "Cardiovascular disease" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a apoptosis, stabilizing cytochrome oxidase, proton trap for oxidative phosphorylation, stabilizing mitochondrial structure that impacts aging. The molecule is a cholesterol translocation that impacts tangier disease, diabetic heart disease, non-alcoholic fatty liver disease, and barth syndrome.
CC/C=C\C/C=C\C/C=C\C/C=C\CCCCC(=O)OC[C@H](COP(=O)(O)OC[C@@H](O)COP(=O)(O)OC[C@@H](COC(=O)CCCCCCCCC/C=C\C/C=C\C/C=C\CC)OC(=O)CCCCCCC/C=C\CCCCCC)OC(=O)CCCCCCC/C=C\CCCCCC
[ "Aging", "Apoptosis", "Stabilizing cytochrome oxidase", "Proton trap for oxidative phosphorylation", "Stabilizing mitochondrial structure", "Tangier disease", "Diabetic heart disease", "Non-alcoholic fatty liver disease", "Cholesterol translocation", "Barth syndrome" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
It has an effect on colorectal cancer, and impacts breast cancer, parkinson's disease, and alzheimer's disease. It impacts seizure, diabetes mellitus, stomach cancer, and cardiovascular disease.
CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)OC[C@H](COP(=O)(O)O[C@@H]1[C@H](O)[C@H](O)[C@@H](O)[C@H](O)[C@H]1O)OC(=O)CCC/C=C\C/C=C\C/C=C\C/C=C\CCC[C@H](C)O
[ "Breast cancer", "Colorectal cancer", "Parkinson's disease", "Alzheimer's Disease", "Seizure", "Diabetes mellitus", "Stomach cancer", "Cardiovascular disease" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a energy source, a membrane stabilizer, and a emulsifier. The molecule is a energy storage, surfactant, signalling molecule, nutrient.
CCCCCCCCCCCCCCC/C=C/C(=O)CC(O)COC(C)=O
[ "Energy source", "Membrane stabilizer", "Emulsifier", "Energy storage", "surfactant", "signalling molecule", "nutrient" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a apoptosis and a proton trap for oxidative phosphorylation that impacts barth syndrome, diabetic heart disease, and non-alcoholic fatty liver disease. The molecule is a stabilizing cytochrome oxidase, stabilizing mitochondrial structure, cholesterol translocation that impacts aging and tangier disease.
CC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CCC(=O)O[C@H](COC(=O)CCCCC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CC)COP(=O)(O)OC[C@@H](O)COP(=O)(O)OC[C@@H](COC(=O)CCCCCCCCC/C=C\C/C=C\CCCCC)OC(=O)CCCC/C=C\C/C=C\C/C=C\C/C=C\CC
[ "Barth syndrome", "Apoptosis", "Diabetic heart disease", "Proton trap for oxidative phosphorylation", "Non-alcoholic fatty liver disease", "Aging", "Stabilizing cytochrome oxidase", "Stabilizing mitochondrial structure", "Cholesterol translocation", "Tangier disease" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a energy source, nutrient, inflammatory that impacts metabolic syndrome, cancer, and atherosclerosis. The molecule is a membrane stabilizer and belongs to the thyroxine treatment class of molecules, impacting cardiovascular disease. The molecule is a energy storage and a fat storage, impacting both obes...
CCC(C)CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCCCCCCC(C)C)OC(=O)CCCCCCCCC(C)CC
[ "Energy source", "nutrient", "Metabolic syndrome", "inflammatory", "Cancer", "Atherosclerosis", "Thyroxine treatment", "Membrane stabilizer", "Cardiovascular disease", "Energy storage", "Obesity", "Fat storage", "Pancreatitis" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a fat storage and thyroxine treatment, and it impacts pancreatitis. The molecule is a nutrient that impacts metabolic syndrome, cardiovascular disease, and atherosclerosis.
CC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CCCCCC(=O)OC[C@H](COC(=O)CCCCCC/C=C\C/C=C\C/C=C\CCCCC)OC(=O)CCCC/C=C\C/C=C\C/C=C\CCCCC
[ "Thyroxine treatment", "Fat storage", "Pancreatitis", "Metabolic syndrome", "Cardiovascular disease", "nutrient", "Atherosclerosis" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a inflammatory and energy storage, belonging to the thyroxine treatment class of molecules, and impacts obesity, atherosclerosis, and pancreatitis. The molecule is a nutrient, a energy source, and a fat storage. The molecule is a membrane stabilizer that impacts metabolic syndrome, cardiovascular diseas...
CCCCCCCCCCCCCCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCCCCCCC
[ "Obesity", "inflammatory", "Energy storage", "Atherosclerosis", "Thyroxine treatment", "Pancreatitis", "nutrient", "Energy source", "Fat storage", "Metabolic syndrome", "Cardiovascular disease", "Membrane stabilizer", "Cancer" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a nutrient that impacts ulcerative colitis, breast cancer, cervical cancer, and atherosclerosis.
CCCCCCCCCCCCCCC(=O)O[C@H](COC(=O)CCC/C=C\C/C=C\C/C=C\C/C=C\CC[C@@H](O)CC)COP(=O)([O-])OCC[N+](C)(C)C
[ "Ulcerative colitis", "Breast cancer", "nutrient", "Cervical cancer", "Atherosclerosis" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a apoptosis and a cholesterol translocation that impacts non-alcoholic fatty liver disease, diabetic heart disease, and tangier disease. The molecule is a proton trap for oxidative phosphorylation, stabilizing mitochondrial structure, stabilizing cytochrome oxidase that impacts aging and barth syndrome.
CCCCC/C=C\C/C=C\CCCCCCCCCC(=O)OC[C@H](COP(=O)(O)OC[C@@H](O)COP(=O)(O)OC[C@@H](COC(=O)CCCCCCCCCCCCCCC)OC(=O)CCCCCCCCC/C=C\C/C=C\CCCCC)OC(=O)CCCCCCCCCCCCC
[ "Apoptosis", "Non-alcoholic fatty liver disease", "Diabetic heart disease", "Tangier disease", "Cholesterol translocation", "Proton trap for oxidative phosphorylation", "Stabilizing mitochondrial structure", "Stabilizing cytochrome oxidase", "Aging", "Barth syndrome" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
It impacts seizure, cardiovascular disease, parkinson's disease, and diabetes mellitus. It has an effect on stomach cancer, and impacts breast cancer, alzheimer's disease, and colorectal cancer.
CCCCC/C=C\C/C=C\C/C=C\C=C\C(=O)CCCC(=O)O[C@H](COC(=O)CCCC/C=C\C/C=C\C/C=C\CCCCC)COP(=O)(O)O[C@H]1C(O)C(O)C(O)[C@@H](OP(=O)(O)O)C1O
[ "Seizure", "Cardiovascular disease", "Parkinson's disease", "Diabetes mellitus", "Breast cancer", "Stomach cancer", "Alzheimer's Disease", "Colorectal cancer" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a cholesterol translocation, stabilizing cytochrome oxidase, proton trap for oxidative phosphorylation that impacts barth syndrome and diabetic heart disease. The molecule is a stabilizing mitochondrial structure and a apoptosis that impacts tangier disease, non-alcoholic fatty liver disease, and aging.
CCCCCCCCCCCCCCCCCCCCCCC(=O)O[C@H](COC(=O)CCCCCCCCCCCCCC(C)C)COP(=O)(O)OC[C@@H](O)COP(=O)(O)OC[C@@H](COC(=O)CCCCCCCCCC(C)C)OC(=O)CCCCCCCCCCCC(C)C
[ "Cholesterol translocation", "Barth syndrome", "Stabilizing cytochrome oxidase", "Proton trap for oxidative phosphorylation", "Diabetic heart disease", "Stabilizing mitochondrial structure", "Tangier disease", "Non-alcoholic fatty liver disease", "Aging", "Apoptosis" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is anti tumor activity.
CC(C)C1=C(C(=O)N2C(C)CCC2C(=O)N2CCN(CCO)C(C)(C)C2)SC2=NC(C)(c3ccc(Cl)cc3)C(c3ccc(Cl)cc3)N21
[ "anti tumor activity" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
It has an effect on breast cancer, and impacts alzheimer's disease, diabetes mellitus, and stomach cancer. It has an effect on colorectal cancer, and impacts parkinson's disease, seizure, and cardiovascular disease.
CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)(O)O[C@@H]1[C@H](O)[C@H](O)[C@@H](O)[C@H](O)[C@H]1O)OC(=O)CCC[C@@H](O)[C@H](O)/C=C\C=C/C=C/C=C/[C@@H](O)C/C=C\CC
[ "Breast cancer", "Alzheimer's Disease", "Diabetes mellitus", "Stomach cancer", "Parkinson's disease", "Seizure", "Cardiovascular disease", "Colorectal cancer" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a cholesterol translocation and a stabilizing mitochondrial structure that impacts tangier disease, non-alcoholic fatty liver disease, and aging. The molecule is a proton trap for oxidative phosphorylation, stabilizing cytochrome oxidase, apoptosis that impacts barth syndrome and diabetic heart disease.
CCCCCCCCCCCCCCCCCCCCCC(=O)O[C@H](COC(=O)CCCCCCCCCCCCCCCCCC)COP(=O)(O)OC[C@@H](O)COP(=O)(O)OC[C@@H](COC(=O)CCCCCCCCCC(C)C)OC(=O)CCCCCCCCCCC(C)C
[ "Tangier disease", "Non-alcoholic fatty liver disease", "Cholesterol translocation", "Stabilizing mitochondrial structure", "Aging", "Barth syndrome", "Diabetic heart disease", "Proton trap for oxidative phosphorylation", "Stabilizing cytochrome oxidase", "Apoptosis" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a membrane stabilizer, inflammatory, fat storage, energy storage that has an effect on cancer and impacts metabolic syndrome. The molecule is a thyroxine treatment and energy source, and it impacts obesity. The molecule is a nutrient that impacts atherosclerosis, cardiovascular disease, and pancreatitis...
CCCCCCCCCCCCCCCCCCCC(=O)OC[C@H](COC(=O)CCCCCCCCCCCCCCCC(C)C)OC(=O)CCCCCCCCCCCCCCCCC(C)CC
[ "Membrane stabilizer", "Metabolic syndrome", "inflammatory", "Fat storage", "Energy storage", "Cancer", "Thyroxine treatment", "Energy source", "Obesity", "Atherosclerosis", "nutrient", "Cardiovascular disease", "Pancreatitis" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
It impacts diabetes mellitus, seizure, parkinson's disease, and colorectal cancer. It has an effect on breast cancer, and impacts alzheimer's disease, cardiovascular disease, and stomach cancer.
CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCCCC(=O)OC[C@H](COP(=O)(O)O[C@H]1C(O)C(O)C(O)[C@@H](OP(=O)(O)O)C1O)OC(=O)CCCCCCC[C@H](O)[C@@H](O)C/C=C\CCCCC
[ "Diabetes mellitus", "Seizure", "Parkinson's disease", "Colorectal cancer", "Alzheimer's Disease", "Breast cancer", "Cardiovascular disease", "Stomach cancer" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a 11beta-hsd1 inhibitor and is metabolic disease treatment.
O=C(O)CC1(Cc2ccccc2Cl)C2CC3CC(C2)CC1C3
[ "11beta-hsd1 inhibitor", "metabolic disease treatment" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
When heated to decomp it emits very toxic fumes of nitrogen oxides and organic fumes.
CN1CCCC1c1cccnc1.CN1CCCC1c1cccnc1.O=S(=O)(O)O
[ "Decomposition_evaluation" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a stabilizing mitochondrial structure, cholesterol translocation, apoptosis that impacts barth syndrome and tangier disease. The molecule is a stabilizing cytochrome oxidase and a proton trap for oxidative phosphorylation that impacts aging, non-alcoholic fatty liver disease, and diabetic heart disease.
CC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CCC(=O)O[C@H](COC(=O)CCCCCCC/C=C\C/C=C\CCCCC)COP(=O)(O)OC[C@H](O)COP(=O)(O)OC[C@@H](COC(=O)CCCCCCC/C=C\CCCCCCCC)OC(=O)CCC/C=C\C/C=C\C/C=C\C/C=C\CCCCC
[ "Stabilizing mitochondrial structure", "Cholesterol translocation", "Apoptosis", "Barth syndrome", "Tangier disease", "Aging", "Non-alcoholic fatty liver disease", "Stabilizing cytochrome oxidase", "Proton trap for oxidative phosphorylation", "Diabetic heart disease" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
It impacts alzheimer's disease, parkinson's disease, colorectal cancer, and stomach cancer. It impacts breast cancer, diabetes mellitus, cardiovascular disease, and seizure.
CC/C=C\C[C@@H](O)/C=C/C=C\C/C=C\C=C\[C@@H](O)/C=C\CCCC(=O)OC[C@H](COP(=O)(O)O[C@H]1C(O)C(O)C(O)[C@@H](OP(=O)(O)O)C1O)OC(=O)CCCCCC/C=C\C/C=C\C/C=C\CCCCC
[ "Alzheimer's Disease", "Parkinson's disease", "Colorectal cancer", "Stomach cancer", "Breast cancer", "Diabetes mellitus", "Cardiovascular disease", "Seizure" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a egfr inhibitor.
C=CC(=O)Nc1cc(Nc2cn3c(C4CC4)cnc3cn2)c(OC)cc1N1CCC(N(C)C)CC1
[ "egfr inhibitor" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a cholesterol translocation, stabilizing cytochrome oxidase, proton trap for oxidative phosphorylation, apoptosis that impacts aging. The molecule is a stabilizing mitochondrial structure that impacts diabetic heart disease, barth syndrome, non-alcoholic fatty liver disease, and tangier disease.
CC/C=C\C/C=C\C/C=C\C/C=C\CCCCC(=O)O[C@H](COC(=O)CCCCCCCCC/C=C\C/C=C\CCCCC)COP(=O)(O)OC[C@@H](O)COP(=O)(O)OC[C@@H](COC(=O)CCCCCCCCC/C=C\C/C=C\CCCCC)OC(=O)CC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CCCCC
[ "Aging", "Cholesterol translocation", "Stabilizing cytochrome oxidase", "Proton trap for oxidative phosphorylation", "Apoptosis", "Diabetic heart disease", "Barth syndrome", "Stabilizing mitochondrial structure", "Non-alcoholic fatty liver disease", "Tangier disease" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a stabilizing cytochrome oxidase, proton trap for oxidative phosphorylation, apoptosis, cholesterol translocation that impacts barth syndrome. The molecule is a stabilizing mitochondrial structure that impacts non-alcoholic fatty liver disease, aging, tangier disease, and diabetic heart disease.
CCCCC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CCC(=O)OC[C@H](COP(=O)(O)OC[C@H](O)COP(=O)(O)OC[C@@H](COC(=O)CCCCCCC/C=C\C/C=C\CCCCC)OC(=O)CCCCCCC/C=C\CCCCCCCC)OC(=O)CCCCCCCCCCCCCCCCC
[ "Stabilizing cytochrome oxidase", "Barth syndrome", "Proton trap for oxidative phosphorylation", "Apoptosis", "Cholesterol translocation", "Non-alcoholic fatty liver disease", "Aging", "Tangier disease", "Stabilizing mitochondrial structure", "Diabetic heart disease" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a proton trap for oxidative phosphorylation, stabilizing cytochrome oxidase, apoptosis that impacts aging and non-alcoholic fatty liver disease. The molecule is a stabilizing mitochondrial structure and a cholesterol translocation that impacts barth syndrome, tangier disease, and diabetic heart disease.
CC/C=C\C/C=C\C/C=C\CCCCCCCCCC(=O)O[C@H](COC(=O)CCC/C=C\C/C=C\C/C=C\C/C=C\CCCCC)COP(=O)(O)OC[C@H](O)COP(=O)(O)OC[C@@H](COC(=O)CCCCCCCCCCCCCCC)OC(=O)CCCCCCCCC/C=C\C/C=C\C/C=C\CC
[ "Proton trap for oxidative phosphorylation", "Aging", "Stabilizing cytochrome oxidase", "Non-alcoholic fatty liver disease", "Apoptosis", "Barth syndrome", "Stabilizing mitochondrial structure", "Cholesterol translocation", "Tangier disease", "Diabetic heart disease" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
It belongs to the s1p1 agonist class of molecules.
CCOc1cccc(Oc2ccc(NC(=O)C(C)(N)CO)cc2)c1
[ "s1p1 agonist" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
Decomposes at melting point.
[Cu+2].[O-][As]([O-])O
[ "Decomposition_evaluation" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a fat storage that impacts both cardiovascular disease and atherosclerosis. The molecule is a nutrient that impacts metabolic syndrome, pancreatitis, and thyroxine treatment.
CC/C=C\C/C=C\C/C=C\C/C=C\CCCCCCC(=O)OC[C@H](COC(=O)CCCCCCC/C=C\CCCCCC)OC(=O)CCCCCCCCCCCCC/C=C\CCCCCCCC
[ "Cardiovascular disease", "Atherosclerosis", "Fat storage", "nutrient", "Metabolic syndrome", "Pancreatitis", "Thyroxine treatment" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a apoptosis and a stabilizing cytochrome oxidase that impacts tangier disease, aging, and non-alcoholic fatty liver disease. The molecule is a proton trap for oxidative phosphorylation, stabilizing mitochondrial structure, cholesterol translocation that impacts barth syndrome and diabetic heart disease.
CCCCCCCCCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)(O)OC[C@@H](O)COP(=O)(O)OC[C@@H](COC(=O)CCCCCCC)OC(=O)CCCCCCCCC(C)C)OC(=O)CCCCCCCCCCCCCCCCCCCCC(C)CC
[ "Apoptosis", "Tangier disease", "Aging", "Stabilizing cytochrome oxidase", "Non-alcoholic fatty liver disease", "Barth syndrome", "Proton trap for oxidative phosphorylation", "Stabilizing mitochondrial structure", "Diabetic heart disease", "Cholesterol translocation" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a kinase inhibitor.
CC(C)(O)c1ccc2c(c1)[nH]c1c(C(N)=O)cc(Cl)c(-c3cccc(-n4c(=O)[nH]c5c(F)cc(F)cc5c4=O)c3)c12
[ "kinase inhibitor" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a cholesterol translocation, stabilizing mitochondrial structure, apoptosis that impacts tangier disease and diabetic heart disease. The molecule is a stabilizing cytochrome oxidase and a proton trap for oxidative phosphorylation that impacts aging, barth syndrome, and non-alcoholic fatty liver disease.
CCCCCC/C=C\C=C/CCCCCCCC(=O)O[C@H](COC(=O)CCCCCCCCCCCCCCCCC)COP(=O)(O)OC[C@@H](O)COP(=O)(O)OC[C@@H](COC(=O)CCCCCCCCCCCCC)OC(=O)CCCCCCCCCCC(C)C
[ "Cholesterol translocation", "Tangier disease", "Stabilizing mitochondrial structure", "Apoptosis", "Diabetic heart disease", "Stabilizing cytochrome oxidase", "Aging", "Proton trap for oxidative phosphorylation", "Barth syndrome", "Non-alcoholic fatty liver disease" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a nutrient that impacts both pancreatitis and cardiovascular disease. The molecule is a fat storage and belongs to the thyroxine treatment class of molecules, impacting both atherosclerosis and metabolic syndrome.
CCCC/C=C\CCCCCCCC(=O)O[C@H](COCCCCCCCCCCCCCCCCCC)COC(=O)CCCCCC/C=C\C/C=C\C/C=C\CCCCC
[ "Pancreatitis", "nutrient", "Cardiovascular disease", "Atherosclerosis", "Thyroxine treatment", "Fat storage", "Metabolic syndrome" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a stabilizing mitochondrial structure, stabilizing cytochrome oxidase, apoptosis that impacts aging and non-alcoholic fatty liver disease. The molecule is a proton trap for oxidative phosphorylation and a cholesterol translocation that impacts tangier disease, barth syndrome, and diabetic heart disease.
CCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)(O)OC[C@H](O)COP(=O)(O)OC[C@@H](COC(=O)CCCCCCC/C=C\CCCCCC)OC(=O)CCCCCCCCCCCCC)OC(=O)CCCCCCC/C=C\CCCCCCCC
[ "Aging", "Stabilizing mitochondrial structure", "Stabilizing cytochrome oxidase", "Apoptosis", "Non-alcoholic fatty liver disease", "Proton trap for oxidative phosphorylation", "Tangier disease", "Barth syndrome", "Cholesterol translocation", "Diabetic heart disease" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a nutrient, sulfury, alliaceous, and roasted. The molecule is a flavoring agent, coffee, smoke, meaty, fishy.
C=C(C=O)[C@@H]1CC[C@]2(C)[C@H]3CCC4[C@@]5(C)CC[C@H](O)C(C)(C)C5CC[C@@]4(C)[C@]3(C)CC[C@@H]12
[ "sulfury", "alliaceous", "roasted", "nutrient", "coffee", "smoke", "meaty", "fishy", "Flavoring agent" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is both a tyrosine kinase inhibitor and a protein kinase inhibitor.
COc1ccc2c(c1)-c1nc(Nc3ccc(OC)c(OCCN(C)C)c3)ncc1CC2(C)C
[ "tyrosine kinase inhibitor", "protein kinase inhibitor" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a cholesterol translocation, stabilizing mitochondrial structure, proton trap for oxidative phosphorylation, apoptosis that impacts tangier disease. The molecule is a stabilizing cytochrome oxidase that impacts diabetic heart disease, barth syndrome, non-alcoholic fatty liver disease, and aging.
CCCCC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CCC(=O)O[C@H](COC(=O)CCCCCCCCCCCCCCCCC)COP(=O)(O)OC[C@H](O)COP(=O)(O)OC[C@@H](COC(=O)CCCCCCCCC/C=C\C/C=C\CCCCC)OC(=O)CCCCCCC/C=C\C/C=C\CCCCC
[ "Cholesterol translocation", "Tangier disease", "Stabilizing mitochondrial structure", "Proton trap for oxidative phosphorylation", "Apoptosis", "Diabetic heart disease", "Barth syndrome", "Stabilizing cytochrome oxidase", "Non-alcoholic fatty liver disease", "Aging" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a membrane stabilizer, surfactant, energy source, emulsifier, energy storage, nutrient.
C[C@@H]1O[C@@H](O[C@H]2[C@H](O[C@H]3[C@H](O[C@H]4CC[C@@]5(C)[C@@H](CC[C@]6(C)[C@@H]5CC=C5[C@@H]7CC(C)(C)C[C@@H](O)[C@]7(C)CC[C@]56C)[C@@]4(C)CO)O[C@H](C(=O)O)[C@@H](O)[C@@H]3O)O[C@H](CO)[C@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O
[ "Membrane stabilizer", "surfactant", "Energy source", "Emulsifier", "Energy storage", "nutrient" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }
The molecule is a fibrosis treatment and is inflammatory disease treatment.
Cc1noc(-c2ccccc2-c2ccc(C3(C(=O)O)CC3)cc2)c1Nc1cncc(-c2ccccc2)c1
[ "fibrosis treatment", "inflammatory disease treatment" ]
{ "Actives": null, "Approval Date": null, "Brand Name": null, "Indication": null, "PubChem CIDs": null }