Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C21H30O3 |
| Molecular Weight | 330.4611 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCCC1=CC(O)=C([C@@H]2C=C(CO)CC[C@H]2C(C)=C)C(O)=C1
InChI
InChIKey=ZELUXPWDPVXUEI-ZWKOTPCHSA-N
InChI=1S/C21H30O3/c1-4-5-6-7-15-11-19(23)21(20(24)12-15)18-10-16(13-22)8-9-17(18)14(2)3/h10-12,17-18,22-24H,2,4-9,13H2,1,3H3/t17-,18+/m0/s1
| Molecular Formula | C21H30O3 |
| Molecular Weight | 330.4611 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 15:09:13 GMT 2023
by
admin
on
Sat Dec 16 15:09:13 GMT 2023
|
| Record UNII |
N38G7JB3K2
|
| Record Status |
Validated (UNII)
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| Record Version |
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-
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Common Name | English | ||
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Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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7-Hydroxycannabidiol
Created by
admin on Sat Dec 16 15:09:13 GMT 2023 , Edited by admin on Sat Dec 16 15:09:13 GMT 2023
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PRIMARY | |||
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11301963
Created by
admin on Sat Dec 16 15:09:13 GMT 2023 , Edited by admin on Sat Dec 16 15:09:13 GMT 2023
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PRIMARY | |||
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N38G7JB3K2
Created by
admin on Sat Dec 16 15:09:13 GMT 2023 , Edited by admin on Sat Dec 16 15:09:13 GMT 2023
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PRIMARY | |||
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50725-17-2
Created by
admin on Sat Dec 16 15:09:13 GMT 2023 , Edited by admin on Sat Dec 16 15:09:13 GMT 2023
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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TARGET -> AGONIST |
Appears to be 5 times more active in preventing seizures than cannabidiol.
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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PARENT -> METABOLITE ACTIVE |
The major circulating metabolites include 7-hydroxy-cannabidiol (7-OH-CBD), which was approximately 38% of the parent based on AUC of cannabidiol.
MAJOR
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