| [ | |
| { | |
| "description": "", | |
| "key": "delta_9_thc", | |
| "name": "Delta-9 THC", | |
| "scientific_name": "\u0394-9-Tetrahydrocannabinol", | |
| "type": "cannabinoid", | |
| "wikipedia_url": "https://en.wikipedia.org/wiki/Tetrahydrocannabinol", | |
| "degrades_to": [], | |
| "precursors": [ | |
| "thca" | |
| ], | |
| "subtype": "", | |
| "CAS_number": "1972-08-3", | |
| "chemical_formula": "C21H30O2", | |
| "molar_mass": 314.469, | |
| "density": null, | |
| "boiling_point": null, | |
| "image_url": "https://huggingface.co/datasets/cannlytics/cannabis_analytes/blob/main/images/cannabinoids/delta_9_thc.png", | |
| "chemical_structure_image_url": "https://huggingface.co/datasets/cannlytics/cannabis_analytes/blob/main/images/cannabinoids/delta_9_thc.svg" | |
| }, | |
| { | |
| "description": "Tetrahydrocannabinolic acid (THCA, 2-COOH-THC; conjugate base tetrahydrocannabinolate) is a precursor of tetrahydrocannabinol (THC), an active component of cannabis.THCA is found in variable quantities in fresh, undried cannabis, but is progressively decarboxylated to THC with drying, and especially under intense heating such as when cannabis is smoked or cooked into cannabis edibles. THCA is often the majority constituent in cannabis resin concentrates, such as hashish and hash oil, when prepared from high-THC cannabis fresh plant material, frequently comprising between 50% and 90% by weight.", | |
| "key": "thca", | |
| "name": "THCA", | |
| "scientific_name": "Tetrahydrocannabinolic acid", | |
| "type": "cannabinoid", | |
| "wikipedia_url": "https://en.wikipedia.org/wiki/Tetrahydrocannabinolic_acid", | |
| "degrades_to": [ | |
| "delta_9_thc" | |
| ], | |
| "precursors": [], | |
| "subtype": "", | |
| "CAS_number": "23978-85-0", | |
| "chemical_formula": "C22H30O4", | |
| "molar_mass": 358.478, | |
| "density": null, | |
| "boiling_point": null, | |
| "image_url": "https://huggingface.co/datasets/cannlytics/cannabis_analytes/blob/main/images/cannabinoids/thca.png", | |
| "chemical_structure_image_url": "https://huggingface.co/datasets/cannlytics/cannabis_analytes/blob/main/images/cannabinoids/thca.svg" | |
| }, | |
| { | |
| "description": "\u0394-8-tetrahydrocannabinol (delta-8-THC, \u03948-THC) is a psychoactive cannabinoid found in the Cannabis plant.", | |
| "key": "delta_8_thc", | |
| "name": "Delta-8 THC", | |
| "scientific_name": "\u0394-8-Tetrahydrocannabinol", | |
| "type": "cannabinoid", | |
| "wikipedia_url": "https://en.wikipedia.org/wiki/Delta-8-Tetrahydrocannabinol", | |
| "degrades_to": [], | |
| "precursors": [], | |
| "subtype": "", | |
| "CAS_number": "5957-75-5", | |
| "chemical_formula": "C21H30O2", | |
| "molar_mass": 314.5, | |
| "density": null, | |
| "boiling_point": null, | |
| "image_url": "https://huggingface.co/datasets/cannlytics/cannabis_analytes/blob/main/images/cannabinoids/delta_8_thc.png", | |
| "chemical_structure_image_url": "https://huggingface.co/datasets/cannlytics/cannabis_analytes/blob/main/images/cannabinoids/delta_8_thc.svg" | |
| }, | |
| { | |
| "description": "Tetrahydrocannabivarin (THCV, THV, O-4394, GWP42004) is a homologue of tetrahydrocannabinol (THC) having a propyl (3-carbon) side chain instead of pentyl (5-carbon), making it non-psychoactive in lower doses. It has been shown to exhibit neuroprotective activity, appetite suppression, glycemic control and reduced side effects compared to THC, making it a potential treatment for management of obesity and diabetes.", | |
| "key": "thcv", | |
| "name": "THCV", | |
| "scientific_name": "Tetrahydrocannabivarin", | |
| "type": "cannabinoid", | |
| "wikipedia_url": "https://en.wikipedia.org/wiki/Tetrahydrocannabivarin", | |
| "degrades_to": [], | |
| "precursors": [ | |
| "thcva" | |
| ], | |
| "subtype": "", | |
| "CAS_number": "31262-37-0", | |
| "chemical_formula": "C19H26O2", | |
| "molar_mass": 286.415, | |
| "density": null, | |
| "boiling_point": null, | |
| "image_url": "https://huggingface.co/datasets/cannlytics/cannabis_analytes/blob/main/images/cannabinoids/thcv.png", | |
| "chemical_structure_image_url": "https://huggingface.co/datasets/cannlytics/cannabis_analytes/blob/main/images/cannabinoids/thcv.svg" | |
| }, | |
| { | |
| "description": "", | |
| "key": "thcva", | |
| "name": "THCVA", | |
| "scientific_name": "Tetrahydrocannabivarinic acid", | |
| "type": "cannabinoid", | |
| "wikipedia_url": "https://en.wikipedia.org/wiki/Tetrahydrocannabivarinic_acid", | |
| "degrades_to": [ | |
| "thcv" | |
| ], | |
| "precursors": [], | |
| "subtype": "", | |
| "CAS_number": "24274-48-4" | |
| }, | |
| { | |
| "description": "Cannabigerol (CBG) is one of more than 120 identified cannabinoid compounds found in the plant genus Cannabis. Cannabigerol is the decarboxylated form of cannabigerolic acid, the parent molecule from which other cannabinoids are synthesized.Cannabigerol is normally a minor constituent of cannabis. During plant growth, most of the cannabigerol is converted into other cannabinoids, primarily tetrahydrocannabinol (THC) or cannabidiol (CBD), leaving about 1% cannabigerol in the plant.", | |
| "key": "cbg", | |
| "name": "CBG", | |
| "scientific_name": "Cannabigerol", | |
| "type": "cannabinoid", | |
| "wikipedia_url": "https://en.wikipedia.org/wiki/Cannabigerol", | |
| "degrades_to": [], | |
| "precursors": [ | |
| "cbga" | |
| ], | |
| "subtype": "", | |
| "CAS_number": "25654-31-3", | |
| "chemical_formula": "C21H32O2", | |
| "molar_mass": 316.485, | |
| "density": null, | |
| "boiling_point": null, | |
| "image_url": "https://huggingface.co/datasets/cannlytics/cannabis_analytes/blob/main/images/cannabinoids/cbg.png", | |
| "chemical_structure_image_url": "https://huggingface.co/datasets/cannlytics/cannabis_analytes/blob/main/images/cannabinoids/cbg.svg" | |
| }, | |
| { | |
| "description": "Cannabigerolic acid (CBGA) is the acidic form of cannabigerol (CBG). It is a dihydroxybenzoic acid and olivetolic acid in which the hydrogen at position 3 is substituted by a geranyl group. It is a biosynthetic precursor to Delta-9-tetrahydrocannabinol, which is the principal psychoactive constituent of the Cannabis plant.", | |
| "key": "cbga", | |
| "name": "CBGA", | |
| "scientific_name": "Cannabigerolic acid", | |
| "type": "cannabinoid", | |
| "wikipedia_url": "https://en.wikipedia.org/wiki/Cannabigerolic_acid", | |
| "degrades_to": [ | |
| "cbg" | |
| ], | |
| "precursors": [], | |
| "subtype": "", | |
| "CAS_number": "25555-57-1", | |
| "chemical_formula": "C22H32O4", | |
| "molar_mass": 360.494, | |
| "density": null, | |
| "boiling_point": null, | |
| "image_url": "https://huggingface.co/datasets/cannlytics/cannabis_analytes/blob/main/images/cannabinoids/cbga.png", | |
| "chemical_structure_image_url": "https://huggingface.co/datasets/cannlytics/cannabis_analytes/blob/main/images/cannabinoids/cbga.svg" | |
| }, | |
| { | |
| "description": "Cannabinol (CBN) is a mildly psychoactive cannabinoid that acts as a low affinity partial agonist at both CB1 and CB2 receptors. This activity at CB1 and CB2 receptors constitutes interaction of CBN with the endocannabinoid system (ECS).\nCBN was the first cannabis compound to be isolated from cannabis extract in the late 1800s.", | |
| "key": "cbn", | |
| "name": "CBN", | |
| "scientific_name": "Cannabinol", | |
| "type": "cannabinoid", | |
| "wikipedia_url": "https://en.wikipedia.org/wiki/Cannabinol", | |
| "degrades_to": [], | |
| "precursors": [], | |
| "subtype": "", | |
| "CAS_number": "521-35-7", | |
| "chemical_formula": "C21H26O2", | |
| "molar_mass": 310.437, | |
| "density": null, | |
| "boiling_point": null, | |
| "image_url": "https://huggingface.co/datasets/cannlytics/cannabis_analytes/blob/main/images/cannabinoids/cbn.png", | |
| "chemical_structure_image_url": "https://huggingface.co/datasets/cannlytics/cannabis_analytes/blob/main/images/cannabinoids/cbn.svg" | |
| }, | |
| { | |
| "description": "Cannabidivarin (CBDV, GWP42006) is a non-intoxicating psychoactive cannabinoid found in Cannabis. It is a homolog (chemistry) of cannabidiol (CBD), with the side-chain shortened by two methylene bridges (CH2 units).\nAlthough cannabidivarin (CBDV) is usually a minor constituent of the cannabinoid profile, enhanced levels of CBDV have been reported in feral populations of C. indica ( = C. sativa ssp.", | |
| "key": "cbdv", | |
| "name": "CBDV", | |
| "scientific_name": "Cannabidivarin", | |
| "type": "cannabinoid", | |
| "wikipedia_url": "https://en.wikipedia.org/wiki/Cannabidivarin", | |
| "degrades_to": [], | |
| "precursors": [ | |
| "cbdva" | |
| ], | |
| "subtype": "", | |
| "CAS_number": "24274-48-4", | |
| "chemical_formula": "C19H26O2", | |
| "molar_mass": 286.415, | |
| "density": null, | |
| "boiling_point": null, | |
| "image_url": "https://huggingface.co/datasets/cannlytics/cannabis_analytes/blob/main/images/cannabinoids/cbdv.png", | |
| "chemical_structure_image_url": "https://huggingface.co/datasets/cannlytics/cannabis_analytes/blob/main/images/cannabinoids/cbdv.svg" | |
| }, | |
| { | |
| "description": "", | |
| "key": "cbdva", | |
| "name": "Cannabidivarinic acid (CBDVA)", | |
| "type": "cannabinoid", | |
| "wikipedia_url": "https://en.wikipedia.org/wiki/Cannabidivarinic_acid", | |
| "degrades_to": [ | |
| "cbdv" | |
| ], | |
| "precursors": [], | |
| "subtype": "", | |
| "CAS_number": "1245629-14-6" | |
| }, | |
| { | |
| "description": "Cannabichromene (CBC), also called cannabichrome, cannanbichromene, pentylcannabichromene or cannabinochromene, exhibits anti-inflammatory properties in vitro, which may, theoretically, contribute to cannabis analgesic effects.\nIt is a phytocannabinoid, one of the hundreds of cannabinoids found in the Cannabis plant. It bears structural similarity to the other natural cannabinoids, including tetrahydrocannabinol (THC), tetrahydrocannabivarin (THCV), cannabidiol (CBD), and cannabinol (CBN), among others.", | |
| "key": "cbc", | |
| "name": "CBC", | |
| "scientific_name": "Cannabichromene", | |
| "type": "cannabinoid", | |
| "wikipedia_url": "https://en.wikipedia.org/wiki/Cannabichromene", | |
| "degrades_to": [], | |
| "precursors": [ | |
| "cbca" | |
| ], | |
| "subtype": "", | |
| "CAS_number": "20675-51-8", | |
| "chemical_formula": "C21H30O2", | |
| "molar_mass": 314.469, | |
| "density": null, | |
| "boiling_point": null, | |
| "image_url": "https://huggingface.co/datasets/cannlytics/cannabis_analytes/blob/main/images/cannabinoids/cbc.png", | |
| "chemical_structure_image_url": "https://huggingface.co/datasets/cannlytics/cannabis_analytes/blob/main/images/cannabinoids/cbc.svg" | |
| }, | |
| { | |
| "description": "", | |
| "key": "cbca", | |
| "name": "CBCA", | |
| "scientific_name": "Cannabichromenenic acid", | |
| "type": "cannabinoid", | |
| "wikipedia_url": "https://en.wikipedia.org/wiki/Cannabichromenic_acid", | |
| "degrades_to": [ | |
| "cbc" | |
| ], | |
| "precursors": [], | |
| "subtype": "", | |
| "CAS_number": "32556-78-4", | |
| "chemical_formula": "C22H30O4", | |
| "molar_mass": 358.478, | |
| "density": null, | |
| "boiling_point": null, | |
| "image_url": "https://huggingface.co/datasets/cannlytics/cannabis_analytes/blob/main/images/cannabinoids/cbca.png", | |
| "chemical_structure_image_url": "https://huggingface.co/datasets/cannlytics/cannabis_analytes/blob/main/images/cannabinoids/cbca.svg" | |
| }, | |
| { | |
| "description": "Cannabichromevarin (CBCV), also known as cannabivarichromene) is one of over 100 variants of cannabinoid chemical compounds that act on cannabinoid receptors. CBCV is a phytocannabinoid found naturally in cannabis, and is a propyl cannabinoid and an effective anticonvulsant and used to treat brain cancer and epilepsyCBCV was first identified at the University of Nagasaki in 1975 from marijuana from Thailand. CBCV is not thought to be psychoactive or impairing in any way, and is believed to be safe for children and adults and is a compound found in medical marijuana.", | |
| "key": "cbcv", | |
| "name": "CBCV", | |
| "scientific_name": "Cannabichromevarin", | |
| "type": "cannabinoid", | |
| "wikipedia_url": "https://en.wikipedia.org/wiki/Cannabichromevarin", | |
| "degrades_to": [], | |
| "precursors": [], | |
| "subtype": "", | |
| "CAS_number": "62248-85-9", | |
| "chemical_formula": "C19H26O2", | |
| "molar_mass": 286.415, | |
| "density": null, | |
| "boiling_point": null, | |
| "image_url": "https://huggingface.co/datasets/cannlytics/cannabis_analytes/blob/main/images/cannabinoids/cbcv.png", | |
| "chemical_structure_image_url": "https://huggingface.co/datasets/cannlytics/cannabis_analytes/blob/main/images/cannabinoids/cbcv.svg" | |
| }, | |
| { | |
| "description": "Cannabitriol ((+)-CBT, (S,S)-9,10-Dihydroxy-\u03946a(10a)-THC) is a phytocannabinoid first isolated in 1966, an oxidation product of tetrahydrocannabinol which has been identified both as a trace component of cannabis and as a metabolite in cannabis users. Its pharmacology has been little studied, though it has been found to act as an antiestrogen and aromatase inhibitor.", | |
| "key": "cbt", | |
| "name": "CBT", | |
| "scientific_name": "Cannabitriol", | |
| "type": "cannabinoid", | |
| "wikipedia_url": "https://en.wikipedia.org/wiki/Cannabitriol", | |
| "degrades_to": [], | |
| "precursors": [], | |
| "subtype": "", | |
| "CAS_number": "52298-89-8", | |
| "chemical_formula": "C21H30O4", | |
| "molar_mass": 346.467, | |
| "density": null, | |
| "boiling_point": null | |
| }, | |
| { | |
| "description": "Cannabicyclol (CBL) is a non-psychoactive cannabinoid found in Cannabis. CBL is a degradative product like cannabinol, with cannabichromene degrading into CBL through natural irradiation or under acid conditions.CBL is not scheduled under the Convention on Psychotropic Substances.", | |
| "key": "cbl", | |
| "name": "CBL", | |
| "scientific_name": "Cannabicyclol", | |
| "type": "cannabinoid", | |
| "wikipedia_url": "https://en.wikipedia.org/wiki/Cannabicyclol", | |
| "degrades_to": [], | |
| "precursors": [], | |
| "subtype": "", | |
| "CAS_number": "55286-91-5", | |
| "chemical_formula": "C21H30O2", | |
| "molar_mass": 314.469, | |
| "density": null, | |
| "boiling_point": null, | |
| "image_url": "https://huggingface.co/datasets/cannlytics/cannabis_analytes/blob/main/images/cannabinoids/cbl.png", | |
| "chemical_structure_image_url": "https://huggingface.co/datasets/cannlytics/cannabis_analytes/blob/main/images/cannabinoids/cbl.svg" | |
| }, | |
| { | |
| "description": "", | |
| "key": "cbla", | |
| "name": "CBLA", | |
| "scientific_name": "Cannabicyclolic acid", | |
| "type": "cannabinoid", | |
| "wikipedia_url": "https://en.wikipedia.org/wiki/Cannabicyclolic_acid", | |
| "degrades_to": [ | |
| "cbl" | |
| ], | |
| "precursors": [], | |
| "subtype": "", | |
| "CAS_number": "22198-35-0" | |
| } | |
| ] |