A-40174 |
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5,5-Dimethyl-8-(3-methyloctan-2-yl)-2-prop-2-ynyl-3,4-dihydro-1H-chromeno[4,3-c]pyridin-10-ol
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Formula | C26H37NO2 |
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Molar mass | 395.587 g·mol−1 |
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3D model (JSmol) | |
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c2c(C(C)(C)CCCCCC)cc(O)c1c2OC(C)(C)C(CC3)=C1CN3CC#C
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InChI=1S/C26H37NO2/c1-7-9-10-11-18(3)19(4)20-15-23(28)25-21-17-27(13-8-2)14-12-22(21)26(5,6)29-24(25)16-20/h2,15-16,18-19,28H,7,9-14,17H2,1,3-6H3 YKey:PNEYWTKVWJBOMD-UHFFFAOYSA-N Y
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N Y (what is this?) (verify) |
A-40174 (SP-1) is an analgesic drug which acts as a potent cannabinoid receptor agonist, and was developed by Abbott Laboratories in the 1970s.[1] It is a structural analog of dronabinol and dimethylheptylpyran.
See also
References
- ^ Razdan RK (2009). "Structure–Activity Relationships of Classical Cannabinoids". In Reggio PR (ed.). The Cannabinoid Receptors. The Receptors. pp. 3–19. doi:10.1007/978-1-59745-503-9_1. ISBN 978-1-58829-712-9.
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Phytocannabinoids (comparison) | Cannabibutols | |
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Cannabichromenes | |
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Cannabicyclols | |
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Cannabidiols | |
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Cannabielsoins | |
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Cannabigerols | |
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Cannabiphorols | |
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Cannabinols |
- CBN
- CBNA
- CBN-C1
- CBN-C2
- CBN-C4
- CBNM
- CBND
- CBNP
- CBVD
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Cannabitriols | |
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Cannabivarins | |
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Delta-3-tetrahydrocannabinols | |
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Delta-4-tetrahydrocannabinols | |
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Delta-7-tetrahydrocannabinols | |
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Delta-8-tetrahydrocannabinols | |
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Delta-9-tetrahydrocannabinols | |
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Delta-10-Tetrahydrocannabinols | |
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Delta-11-Tetrahydrocannabinols | |
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Miscellaneous cannabinoids | |
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Active metabolites | |
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Endocannabinoids | |
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Synthetic cannabinoid receptor agonists / neocannabinoids | Classical cannabinoids (dibenzopyrans) | |
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Non-classical cannabinoids | |
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Adamantoylindoles | |
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Benzoylindoles | |
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Phenylacetylindoles | |
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Allosteric CBRTooltip Cannabinoid receptor ligands | |
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Endocannabinoid enhancers (inactivation inhibitors) | |
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Anticannabinoids (antagonists/inverse agonists/antibodies) | |
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