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
Molecular Formula | C22H30O4 |
Molecular Weight | 358.4712 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
NMR assignments of the major cannabinoids and cannabiflavonoids isolated from flowers of Cannabis sativa. | 2004 Nov-Dec |
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Cannabidiolic acid as a selective cyclooxygenase-2 inhibitory component in cannabis. | 2008 Sep |
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Down-regulation of cyclooxygenase-2 (COX-2) by cannabidiolic acid in human breast cancer cells. | 2014 |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:35:12 GMT 2023
by
admin
on
Sat Dec 16 08:35:12 GMT 2023
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Record UNII |
FJX8O3OJCD
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Record Status |
Validated (UNII)
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Record Version |
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67136
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1244-58-2
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160570
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DTXSID80154318
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FJX8O3OJCD
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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
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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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Related Record | Type | Details | ||
---|---|---|---|---|
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PARENT -> ACTIVE CONSTITUENT ALWAYS PRESENT |
Cannabidiolic Class | Antibiotic
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