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16,16-dimethylprostaglandin e2 is a stable derivative of prostaglandin e2 (pge2) with potential hematopoietic activity. administration of 16,16 dimethyl-prostaglandin e2 (dmpge2) appears to lead to increased formation of hematopoietic stem and progenitor cells. even though the exact mechanism of action has yet to be fu... |
16,16 dimethylprostaglandin e2 is a synthetic prostaglandin e analog that protects the gastric mucosa, prevents ulceration, and promotes the healing of peptic ulcers. the protective effect is independent of acid inhibition. it is also a potent inhibitor of pancreatic function and growth of experimental tumors. |
16,16 dimethylprostaglandin e2 is a stable derivative of prostaglandin e2 (pge2) with potential hematopoietic activity. administration of 16,16 dimethyl-prostaglandin e2 (dmpge2) appears to lead to increased formation of hematopoietic stem and progenitor cells. even though the exact mechanism of action has yet to be fu... |
16,16 dimethylprostaglandin e2 is a stable derivative of prostaglandin e2 (pge2) with potential hematopoietic activity. administration of 16,16 dimethyl-prostaglandin e2 (dmpge2) appears to lead to increased formation of hematopoietic stem and progenitor cells. even though the exact mechanism of action has yet to be fu... |
e2, 16,16-dimethylprostaglandin is a synthetic prostaglandin e analog that protects the gastric mucosa, prevents ulceration, and promotes the healing of peptic ulcers. the protective effect is independent of acid inhibition. it is also a potent inhibitor of pancreatic function and growth of experimental tumors. |
e2, 16,16-dimethylprostaglandin is a stable derivative of prostaglandin e2 (pge2) with potential hematopoietic activity. administration of 16,16 dimethyl-prostaglandin e2 (dmpge2) appears to lead to increased formation of hematopoietic stem and progenitor cells. even though the exact mechanism of action has yet to be f... |
e2, 16,16-dimethylprostaglandin is a stable derivative of prostaglandin e2 (pge2) with potential hematopoietic activity. administration of 16,16 dimethyl-prostaglandin e2 (dmpge2) appears to lead to increased formation of hematopoietic stem and progenitor cells. even though the exact mechanism of action has yet to be f... |
16,16-dimethyl-pge2 is a synthetic prostaglandin e analog that protects the gastric mucosa, prevents ulceration, and promotes the healing of peptic ulcers. the protective effect is independent of acid inhibition. it is also a potent inhibitor of pancreatic function and growth of experimental tumors. |
16,16-dimethyl-pge2 is a stable derivative of prostaglandin e2 (pge2) with potential hematopoietic activity. administration of 16,16 dimethyl-prostaglandin e2 (dmpge2) appears to lead to increased formation of hematopoietic stem and progenitor cells. even though the exact mechanism of action has yet to be fully elucida... |
16,16-dimethyl-pge2 is a stable derivative of prostaglandin e2 (pge2) with potential hematopoietic activity. administration of 16,16 dimethyl-prostaglandin e2 (dmpge2) appears to lead to increased formation of hematopoietic stem and progenitor cells. even though the exact mechanism of action has yet to be fully elucida... |
16,16 dimethyl pge2 is a synthetic prostaglandin e analog that protects the gastric mucosa, prevents ulceration, and promotes the healing of peptic ulcers. the protective effect is independent of acid inhibition. it is also a potent inhibitor of pancreatic function and growth of experimental tumors. |
16,16 dimethyl pge2 is a stable derivative of prostaglandin e2 (pge2) with potential hematopoietic activity. administration of 16,16 dimethyl-prostaglandin e2 (dmpge2) appears to lead to increased formation of hematopoietic stem and progenitor cells. even though the exact mechanism of action has yet to be fully elucida... |
16,16 dimethyl pge2 is a stable derivative of prostaglandin e2 (pge2) with potential hematopoietic activity. administration of 16,16 dimethyl-prostaglandin e2 (dmpge2) appears to lead to increased formation of hematopoietic stem and progenitor cells. even though the exact mechanism of action has yet to be fully elucida... |
prosta-5,13-dien-1-oic acid, 11,15-dihydroxy-16,16-dimethyl-9-oxo-, (5z,11alpha,13e,15r)- is a synthetic prostaglandin e analog that protects the gastric mucosa, prevents ulceration, and promotes the healing of peptic ulcers. the protective effect is independent of acid inhibition. it is also a potent inhibitor of panc... |
prosta-5,13-dien-1-oic acid, 11,15-dihydroxy-16,16-dimethyl-9-oxo-, (5z,11alpha,13e,15r)- is a stable derivative of prostaglandin e2 (pge2) with potential hematopoietic activity. administration of 16,16 dimethyl-prostaglandin e2 (dmpge2) appears to lead to increased formation of hematopoietic stem and progenitor cells.... |
prosta-5,13-dien-1-oic acid, 11,15-dihydroxy-16,16-dimethyl-9-oxo-, (5z,11alpha,13e,15r)- is a stable derivative of prostaglandin e2 (pge2) with potential hematopoietic activity. administration of 16,16 dimethyl-prostaglandin e2 (dmpge2) appears to lead to increased formation of hematopoietic stem and progenitor cells.... |
16,16-dimethyl prostaglandin e2 is a synthetic prostaglandin e analog that protects the gastric mucosa, prevents ulceration, and promotes the healing of peptic ulcers. the protective effect is independent of acid inhibition. it is also a potent inhibitor of pancreatic function and growth of experimental tumors. |
16,16-dimethyl prostaglandin e2 is a stable derivative of prostaglandin e2 (pge2) with potential hematopoietic activity. administration of 16,16 dimethyl-prostaglandin e2 (dmpge2) appears to lead to increased formation of hematopoietic stem and progenitor cells. even though the exact mechanism of action has yet to be f... |
16,16-dimethyl prostaglandin e2 is a stable derivative of prostaglandin e2 (pge2) with potential hematopoietic activity. administration of 16,16 dimethyl-prostaglandin e2 (dmpge2) appears to lead to increased formation of hematopoietic stem and progenitor cells. even though the exact mechanism of action has yet to be f... |
16, 16-dimethyl prostaglandin e2 is a synthetic prostaglandin e analog that protects the gastric mucosa, prevents ulceration, and promotes the healing of peptic ulcers. the protective effect is independent of acid inhibition. it is also a potent inhibitor of pancreatic function and growth of experimental tumors. |
16, 16-dimethyl prostaglandin e2 is a stable derivative of prostaglandin e2 (pge2) with potential hematopoietic activity. administration of 16,16 dimethyl-prostaglandin e2 (dmpge2) appears to lead to increased formation of hematopoietic stem and progenitor cells. even though the exact mechanism of action has yet to be ... |
16, 16-dimethyl prostaglandin e2 is a stable derivative of prostaglandin e2 (pge2) with potential hematopoietic activity. administration of 16,16 dimethyl-prostaglandin e2 (dmpge2) appears to lead to increased formation of hematopoietic stem and progenitor cells. even though the exact mechanism of action has yet to be ... |
dmpge2 is a synthetic prostaglandin e analog that protects the gastric mucosa, prevents ulceration, and promotes the healing of peptic ulcers. the protective effect is independent of acid inhibition. it is also a potent inhibitor of pancreatic function and growth of experimental tumors. |
dmpge2 is a stable derivative of prostaglandin e2 (pge2) with potential hematopoietic activity. administration of 16,16 dimethyl-prostaglandin e2 (dmpge2) appears to lead to increased formation of hematopoietic stem and progenitor cells. even though the exact mechanism of action has yet to be fully elucidated, this age... |
dmpge2 is a stable derivative of prostaglandin e2 (pge2) with potential hematopoietic activity. administration of 16,16 dimethyl-prostaglandin e2 (dmpge2) appears to lead to increased formation of hematopoietic stem and progenitor cells. even though the exact mechanism of action has yet to be fully elucidated, this age... |
17-hydroxycorticosteroids is a group of hydroxycorticosteroids bearing a hydroxy group at the 17-position. urinary excretion of these compounds is used as an index of adrenal function. they are used systemically in the free alcohol form, but with esterification of the hydroxy groups, topical effectiveness is increased. |
17-hydroxycorticosteroid is a group of hydroxycorticosteroids bearing a hydroxy group at the 17-position. urinary excretion of these compounds is used as an index of adrenal function. they are used systemically in the free alcohol form, but with esterification of the hydroxy groups, topical effectiveness is increased. |
17 hydroxycorticosteroids is a group of hydroxycorticosteroids bearing a hydroxy group at the 17-position. urinary excretion of these compounds is used as an index of adrenal function. they are used systemically in the free alcohol form, but with esterification of the hydroxy groups, topical effectiveness is increased. |
17 hydroxycorticosteroid is a group of hydroxycorticosteroids bearing a hydroxy group at the 17-position. urinary excretion of these compounds is used as an index of adrenal function. they are used systemically in the free alcohol form, but with esterification of the hydroxy groups, topical effectiveness is increased. |
17-hydrocorticosteroid is a group of hydroxycorticosteroids bearing a hydroxy group at the 17-position. urinary excretion of these compounds is used as an index of adrenal function. they are used systemically in the free alcohol form, but with esterification of the hydroxy groups, topical effectiveness is increased. |
17-hydrocorticosteroids is a group of hydroxycorticosteroids bearing a hydroxy group at the 17-position. urinary excretion of these compounds is used as an index of adrenal function. they are used systemically in the free alcohol form, but with esterification of the hydroxy groups, topical effectiveness is increased. |
17-hydroxycorticoid is a group of hydroxycorticosteroids bearing a hydroxy group at the 17-position. urinary excretion of these compounds is used as an index of adrenal function. they are used systemically in the free alcohol form, but with esterification of the hydroxy groups, topical effectiveness is increased. |
17-hydroxycorticoids is a group of hydroxycorticosteroids bearing a hydroxy group at the 17-position. urinary excretion of these compounds is used as an index of adrenal function. they are used systemically in the free alcohol form, but with esterification of the hydroxy groups, topical effectiveness is increased. |
17-hydroxycorticoids, nos is a group of hydroxycorticosteroids bearing a hydroxy group at the 17-position. urinary excretion of these compounds is used as an index of adrenal function. they are used systemically in the free alcohol form, but with esterification of the hydroxy groups, topical effectiveness is increased. |
17 hydroxycorticoids is a group of hydroxycorticosteroids bearing a hydroxy group at the 17-position. urinary excretion of these compounds is used as an index of adrenal function. they are used systemically in the free alcohol form, but with esterification of the hydroxy groups, topical effectiveness is increased. |
17-ketogenic steroids, nos is a group of hydroxycorticosteroids bearing a hydroxy group at the 17-position. urinary excretion of these compounds is used as an index of adrenal function. they are used systemically in the free alcohol form, but with esterification of the hydroxy groups, topical effectiveness is increased... |
17-ketogenic steroids is a group of hydroxycorticosteroids bearing a hydroxy group at the 17-position. urinary excretion of these compounds is used as an index of adrenal function. they are used systemically in the free alcohol form, but with esterification of the hydroxy groups, topical effectiveness is increased. |
17-ketogenic steroid is a group of hydroxycorticosteroids bearing a hydroxy group at the 17-position. urinary excretion of these compounds is used as an index of adrenal function. they are used systemically in the free alcohol form, but with esterification of the hydroxy groups, topical effectiveness is increased. |
17-oxogenic steroids is a group of hydroxycorticosteroids bearing a hydroxy group at the 17-position. urinary excretion of these compounds is used as an index of adrenal function. they are used systemically in the free alcohol form, but with esterification of the hydroxy groups, topical effectiveness is increased. |
17kgs - 17-ketogenic steroids is a group of hydroxycorticosteroids bearing a hydroxy group at the 17-position. urinary excretion of these compounds is used as an index of adrenal function. they are used systemically in the free alcohol form, but with esterification of the hydroxy groups, topical effectiveness is increa... |
17-hydroxycorticosteroid (substance) is a group of hydroxycorticosteroids bearing a hydroxy group at the 17-position. urinary excretion of these compounds is used as an index of adrenal function. they are used systemically in the free alcohol form, but with esterification of the hydroxy groups, topical effectiveness is... |
17-hydroxysteroid dehydrogenases is a class of enzymes that catalyzes the oxidation of 17-hydroxysteroids to 17-ketosteroids. ec 1.1.-. |
17 hydroxysteroid dehydrogenases is a class of enzymes that catalyzes the oxidation of 17-hydroxysteroids to 17-ketosteroids. ec 1.1.-. |
17-hydroxysteroid dehydrogenase is a class of enzymes that catalyzes the oxidation of 17-hydroxysteroids to 17-ketosteroids. ec 1.1.-. |
dehydrogenases, 17-hydroxysteroid is a class of enzymes that catalyzes the oxidation of 17-hydroxysteroids to 17-ketosteroids. ec 1.1.-. |
17-ketosteroid reductases is a class of enzymes that catalyzes the oxidation of 17-hydroxysteroids to 17-ketosteroids. ec 1.1.-. |
17 ketosteroid reductases is a class of enzymes that catalyzes the oxidation of 17-hydroxysteroids to 17-ketosteroids. ec 1.1.-. |
reductases, 17-ketosteroid is a class of enzymes that catalyzes the oxidation of 17-hydroxysteroids to 17-ketosteroids. ec 1.1.-. |
17-ketosteroids is steroids that contain a ketone group at position 17. |
17 ketosteroids is steroids that contain a ketone group at position 17. |
17-ketosteroids, nos is steroids that contain a ketone group at position 17. |
17 ketosteroid is steroids that contain a ketone group at position 17. |
17-ketosteroid is steroids that contain a ketone group at position 17. |
17-oxosteroids is steroids that contain a ketone group at position 17. |
17 oxosteroids is steroids that contain a ketone group at position 17. |
17-oxosteroid is steroids that contain a ketone group at position 17. |
17-ketosteroid (substance) is steroids that contain a ketone group at position 17. |
18-hydroxycorticosterone is 11 beta,18,21-trihydroxypregn-4-ene-3,20-dione. |
18 hydroxycorticosterone is 11 beta,18,21-trihydroxypregn-4-ene-3,20-dione. |
hydroxycorticosterone, 18 is 11 beta,18,21-trihydroxypregn-4-ene-3,20-dione. |
18-hydrocorticosterone is 11 beta,18,21-trihydroxypregn-4-ene-3,20-dione. |
18 hydrocorticosterone is 11 beta,18,21-trihydroxypregn-4-ene-3,20-dione. |
pregn-4-ene-3,20-dione, 11,18,21-trihydroxy-, (11beta)- is 11 beta,18,21-trihydroxypregn-4-ene-3,20-dione. |
11-beta,18,21-trihydroxypregn-4-ene-3,20-dione is 11 beta,18,21-trihydroxypregn-4-ene-3,20-dione. |
18-hydroxycorticosterone (substance) is 11 beta,18,21-trihydroxypregn-4-ene-3,20-dione. |
18-hydroxydesoxycorticosterone is an analog of desoxycorticosterone which is substituted by a hydroxyl group at the c-18 position. |
18 hydroxydesoxycorticosterone is an analog of desoxycorticosterone which is substituted by a hydroxyl group at the c-18 position. |
hydroxydesoxycorticosterone, 18 is an analog of desoxycorticosterone which is substituted by a hydroxyl group at the c-18 position. |
18-hydroxy-11-desoxycorticosterone is an analog of desoxycorticosterone which is substituted by a hydroxyl group at the c-18 position. |
18 hydroxy 11 desoxycorticosterone is an analog of desoxycorticosterone which is substituted by a hydroxyl group at the c-18 position. |
18-hydroxy-11-deoxycorticosterone is an analog of desoxycorticosterone which is substituted by a hydroxyl group at the c-18 position. |
18 hydroxy 11 deoxycorticosterone is an analog of desoxycorticosterone which is substituted by a hydroxyl group at the c-18 position. |
19-iodocholesterol is 19-iodocholest-5-en-3 beta-ol. a cholesterol derivative usually substituted with radioactive iodine in the 19 position. the compound is an adrenal cortex scanning agent used in the assessment of patients suspected of having cushing's syndrome, hyperaldosteronism, pheochromocytoma and adrenal remna... |
19 iodocholesterol is 19-iodocholest-5-en-3 beta-ol. a cholesterol derivative usually substituted with radioactive iodine in the 19 position. the compound is an adrenal cortex scanning agent used in the assessment of patients suspected of having cushing's syndrome, hyperaldosteronism, pheochromocytoma and adrenal remna... |
cholest-5-en-3-ol, 19-(iodo-125i)-, (3beta)- is 19-iodocholest-5-en-3 beta-ol. a cholesterol derivative usually substituted with radioactive iodine in the 19 position. the compound is an adrenal cortex scanning agent used in the assessment of patients suspected of having cushing's syndrome, hyperaldosteronism, pheochro... |
2',3'-cyclic-nucleotide phosphodiesterases is nucleoside-2',3'-cyclic phosphate nucleotidohydrolase. enzymes that catalyze the hydrolysis of the 2'- or 3'- phosphate bonds of 2',3'-cyclic nucleotides. also hydrolyzes nucleoside monophosphates. includes ec 3.1.4.16 and ec 3.1.4.37. ec 3.1.4.-. |
2',3' cyclic nucleotide phosphodiesterase is nucleoside-2',3'-cyclic phosphate nucleotidohydrolase. enzymes that catalyze the hydrolysis of the 2'- or 3'- phosphate bonds of 2',3'-cyclic nucleotides. also hydrolyzes nucleoside monophosphates. includes ec 3.1.4.16 and ec 3.1.4.37. ec 3.1.4.-. |
2',3' cyclic nucleotide phosphodiesterases is nucleoside-2',3'-cyclic phosphate nucleotidohydrolase. enzymes that catalyze the hydrolysis of the 2'- or 3'- phosphate bonds of 2',3'-cyclic nucleotides. also hydrolyzes nucleoside monophosphates. includes ec 3.1.4.16 and ec 3.1.4.37. ec 3.1.4.-. |
2',3'-cyclic nucleotide phosphodiesterase is nucleoside-2',3'-cyclic phosphate nucleotidohydrolase. enzymes that catalyze the hydrolysis of the 2'- or 3'- phosphate bonds of 2',3'-cyclic nucleotides. also hydrolyzes nucleoside monophosphates. includes ec 3.1.4.16 and ec 3.1.4.37. ec 3.1.4.-. |
2',3'-cyclic nucleotide phosphodiesterases is nucleoside-2',3'-cyclic phosphate nucleotidohydrolase. enzymes that catalyze the hydrolysis of the 2'- or 3'- phosphate bonds of 2',3'-cyclic nucleotides. also hydrolyzes nucleoside monophosphates. includes ec 3.1.4.16 and ec 3.1.4.37. ec 3.1.4.-. |
2,3 cyclic nucleotide phosphodiesterase is nucleoside-2',3'-cyclic phosphate nucleotidohydrolase. enzymes that catalyze the hydrolysis of the 2'- or 3'- phosphate bonds of 2',3'-cyclic nucleotides. also hydrolyzes nucleoside monophosphates. includes ec 3.1.4.16 and ec 3.1.4.37. ec 3.1.4.-. |
2,3 cyclic nucleotide phosphodiesterases is nucleoside-2',3'-cyclic phosphate nucleotidohydrolase. enzymes that catalyze the hydrolysis of the 2'- or 3'- phosphate bonds of 2',3'-cyclic nucleotides. also hydrolyzes nucleoside monophosphates. includes ec 3.1.4.16 and ec 3.1.4.37. ec 3.1.4.-. |
2,3-cyclic nucleotide phosphodiesterase is nucleoside-2',3'-cyclic phosphate nucleotidohydrolase. enzymes that catalyze the hydrolysis of the 2'- or 3'- phosphate bonds of 2',3'-cyclic nucleotides. also hydrolyzes nucleoside monophosphates. includes ec 3.1.4.16 and ec 3.1.4.37. ec 3.1.4.-. |
2,3-cyclic nucleotide phosphodiesterases is nucleoside-2',3'-cyclic phosphate nucleotidohydrolase. enzymes that catalyze the hydrolysis of the 2'- or 3'- phosphate bonds of 2',3'-cyclic nucleotides. also hydrolyzes nucleoside monophosphates. includes ec 3.1.4.16 and ec 3.1.4.37. ec 3.1.4.-. |
2'3' cyclic nucleotide phosphodiesterase is nucleoside-2',3'-cyclic phosphate nucleotidohydrolase. enzymes that catalyze the hydrolysis of the 2'- or 3'- phosphate bonds of 2',3'-cyclic nucleotides. also hydrolyzes nucleoside monophosphates. includes ec 3.1.4.16 and ec 3.1.4.37. ec 3.1.4.-. |
nucleotide phosphodiesterase, 2',3'-cyclic is nucleoside-2',3'-cyclic phosphate nucleotidohydrolase. enzymes that catalyze the hydrolysis of the 2'- or 3'- phosphate bonds of 2',3'-cyclic nucleotides. also hydrolyzes nucleoside monophosphates. includes ec 3.1.4.16 and ec 3.1.4.37. ec 3.1.4.-. |
nucleotide phosphodiesterase, 2,3-cyclic is nucleoside-2',3'-cyclic phosphate nucleotidohydrolase. enzymes that catalyze the hydrolysis of the 2'- or 3'- phosphate bonds of 2',3'-cyclic nucleotides. also hydrolyzes nucleoside monophosphates. includes ec 3.1.4.16 and ec 3.1.4.37. ec 3.1.4.-. |
phosphodiesterase, 2',3'-cyclic nucleotide is nucleoside-2',3'-cyclic phosphate nucleotidohydrolase. enzymes that catalyze the hydrolysis of the 2'- or 3'- phosphate bonds of 2',3'-cyclic nucleotides. also hydrolyzes nucleoside monophosphates. includes ec 3.1.4.16 and ec 3.1.4.37. ec 3.1.4.-. |
phosphodiesterase, 2,3-cyclic nucleotide is nucleoside-2',3'-cyclic phosphate nucleotidohydrolase. enzymes that catalyze the hydrolysis of the 2'- or 3'- phosphate bonds of 2',3'-cyclic nucleotides. also hydrolyzes nucleoside monophosphates. includes ec 3.1.4.16 and ec 3.1.4.37. ec 3.1.4.-. |
cyclic 2',3'-nucleotide phosphodiesterase is nucleoside-2',3'-cyclic phosphate nucleotidohydrolase. enzymes that catalyze the hydrolysis of the 2'- or 3'- phosphate bonds of 2',3'-cyclic nucleotides. also hydrolyzes nucleoside monophosphates. includes ec 3.1.4.16 and ec 3.1.4.37. ec 3.1.4.-. |
nucleotide phosphodiesterases, 2',3'-cyclic is nucleoside-2',3'-cyclic phosphate nucleotidohydrolase. enzymes that catalyze the hydrolysis of the 2'- or 3'- phosphate bonds of 2',3'-cyclic nucleotides. also hydrolyzes nucleoside monophosphates. includes ec 3.1.4.16 and ec 3.1.4.37. ec 3.1.4.-. |
phosphodiesterases, 2',3'-cyclic nucleotide is nucleoside-2',3'-cyclic phosphate nucleotidohydrolase. enzymes that catalyze the hydrolysis of the 2'- or 3'- phosphate bonds of 2',3'-cyclic nucleotides. also hydrolyzes nucleoside monophosphates. includes ec 3.1.4.16 and ec 3.1.4.37. ec 3.1.4.-. |
phosphodiesterases, 2',3'-cyclic-nucleotide is nucleoside-2',3'-cyclic phosphate nucleotidohydrolase. enzymes that catalyze the hydrolysis of the 2'- or 3'- phosphate bonds of 2',3'-cyclic nucleotides. also hydrolyzes nucleoside monophosphates. includes ec 3.1.4.16 and ec 3.1.4.37. ec 3.1.4.-. |
phosphodiesterases, 2,3-cyclic nucleotide is nucleoside-2',3'-cyclic phosphate nucleotidohydrolase. enzymes that catalyze the hydrolysis of the 2'- or 3'- phosphate bonds of 2',3'-cyclic nucleotides. also hydrolyzes nucleoside monophosphates. includes ec 3.1.4.16 and ec 3.1.4.37. ec 3.1.4.-. |
nucleotide phosphodiesterases, 2,3-cyclic is nucleoside-2',3'-cyclic phosphate nucleotidohydrolase. enzymes that catalyze the hydrolysis of the 2'- or 3'- phosphate bonds of 2',3'-cyclic nucleotides. also hydrolyzes nucleoside monophosphates. includes ec 3.1.4.16 and ec 3.1.4.37. ec 3.1.4.-. |
cnpase is nucleoside-2',3'-cyclic phosphate nucleotidohydrolase. enzymes that catalyze the hydrolysis of the 2'- or 3'- phosphate bonds of 2',3'-cyclic nucleotides. also hydrolyzes nucleoside monophosphates. includes ec 3.1.4.16 and ec 3.1.4.37. ec 3.1.4.-. |
2-5a synthetase is an enzyme that catalyzes the conversion of atp into a series of (2'-5') linked oligoadenylates and pyrophosphate in the presence of double-stranded rna. these oligonucleotides activate an endoribonuclease (rnase l) which cleaves single-stranded rna. interferons can act as inducers of these reactions. |
2',5'-oligoadenylate synthetase is an enzyme that catalyzes the conversion of atp into a series of (2'-5') linked oligoadenylates and pyrophosphate in the presence of double-stranded rna. these oligonucleotides activate an endoribonuclease (rnase l) which cleaves single-stranded rna. interferons can act as inducers of ... |
2,5 oligoadenylate synthetase is an enzyme that catalyzes the conversion of atp into a series of (2'-5') linked oligoadenylates and pyrophosphate in the presence of double-stranded rna. these oligonucleotides activate an endoribonuclease (rnase l) which cleaves single-stranded rna. interferons can act as inducers of th... |
2',5' oligoadenylate synthetase is an enzyme that catalyzes the conversion of atp into a series of (2'-5') linked oligoadenylates and pyrophosphate in the presence of double-stranded rna. these oligonucleotides activate an endoribonuclease (rnase l) which cleaves single-stranded rna. interferons can act as inducers of ... |
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