Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C22H30O4 |
Molecular Weight | 358.4712 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCCC1=C(C(O)=O)C(O)=C([C@@H]2C=C(C)CC[C@H]2C(C)=C)C(O)=C1
InChI
InChIKey=WVOLTBSCXRRQFR-DLBZAZTESA-N
InChI=1S/C22H30O4/c1-5-6-7-8-15-12-18(23)20(21(24)19(15)22(25)26)17-11-14(4)9-10-16(17)13(2)3/h11-12,16-17,23-24H,2,5-10H2,1,3-4H3,(H,25,26)/t16-,17+/m0/s1
Approval Year
PubMed
Title | Date | PubMed |
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Metabolomic differentiation of Cannabis sativa cultivars using 1H NMR spectroscopy and principal component analysis. | 2004 Jun |
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Cannabinoids act as necrosis-inducing factors in Cannabis sativa. | 2008 Dec |
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Cannabidiolic acid as a selective cyclooxygenase-2 inhibitory component in cannabis. | 2008 Sep |
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Identification of candidate genes affecting Delta9-tetrahydrocannabinol biosynthesis in Cannabis sativa. | 2009 |
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Standardized cannabis in multiple sclerosis: a case report. | 2010 Jan 6 |
Patents
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Code System | Code | Type | Description | ||
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67136
Created by
admin on Sat Dec 16 08:35:12 GMT 2023 , Edited by admin on Sat Dec 16 08:35:12 GMT 2023
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1244-58-2
Created by
admin on Sat Dec 16 08:35:12 GMT 2023 , Edited by admin on Sat Dec 16 08:35:12 GMT 2023
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160570
Created by
admin on Sat Dec 16 08:35:12 GMT 2023 , Edited by admin on Sat Dec 16 08:35:12 GMT 2023
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DTXSID80154318
Created by
admin on Sat Dec 16 08:35:12 GMT 2023 , Edited by admin on Sat Dec 16 08:35:12 GMT 2023
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FJX8O3OJCD
Created by
admin on Sat Dec 16 08:35:12 GMT 2023 , Edited by admin on Sat Dec 16 08:35:12 GMT 2023
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3359
Created by
admin on Sat Dec 16 08:35:12 GMT 2023 , Edited by admin on Sat Dec 16 08:35:12 GMT 2023
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Cannabidiolic acid
Created by
admin on Sat Dec 16 08:35:12 GMT 2023 , Edited by admin on Sat Dec 16 08:35:12 GMT 2023
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PRIMARY |
SUBSTANCE RECORD