Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C21H28O2 |
Molecular Weight | 312.4458 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 6 / 6 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@@]12CC[C@@](O)(C#C)[C@@]1(C)CC[C@]3([H])C4=C(C[C@@H](C)[C@@]23[H])CC(=O)CC4
InChI
InChIKey=WZDGZWOAQTVYBX-XOINTXKNSA-N
InChI=1S/C21H28O2/c1-4-21(23)10-8-18-19-13(2)11-14-12-15(22)5-6-16(14)17(19)7-9-20(18,21)3/h1,13,17-19,23H,5-12H2,2-3H3/t13-,17-,18+,19-,20+,21+/m1/s1
Molecular Formula | C21H28O2 |
Molecular Weight | 312.4458 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 6 / 6 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:21:22 UTC 2023
by
admin
on
Fri Dec 15 15:21:22 UTC 2023
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Record UNII |
FF9X0205V2
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Record Status |
Validated (UNII)
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Record Version |
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-
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Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C2360
Created by
admin on Fri Dec 15 15:21:22 UTC 2023 , Edited by admin on Fri Dec 15 15:21:22 UTC 2023
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LIVERTOX |
NBK548180
Created by
admin on Fri Dec 15 15:21:22 UTC 2023 , Edited by admin on Fri Dec 15 15:21:22 UTC 2023
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WHO-ATC |
G03CX01
Created by
admin on Fri Dec 15 15:21:22 UTC 2023 , Edited by admin on Fri Dec 15 15:21:22 UTC 2023
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WHO-VATC |
QG03CX01
Created by
admin on Fri Dec 15 15:21:22 UTC 2023 , Edited by admin on Fri Dec 15 15:21:22 UTC 2023
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Code System | Code | Type | Description | ||
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C66955
Created by
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PRIMARY | |||
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2655
Created by
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PRIMARY | |||
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5630-53-5
Created by
admin on Fri Dec 15 15:21:22 UTC 2023 , Edited by admin on Fri Dec 15 15:21:22 UTC 2023
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PRIMARY | |||
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m10852
Created by
admin on Fri Dec 15 15:21:22 UTC 2023 , Edited by admin on Fri Dec 15 15:21:22 UTC 2023
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PRIMARY | Merck Index | ||
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2777
Created by
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PRIMARY | |||
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38260
Created by
admin on Fri Dec 15 15:21:22 UTC 2023 , Edited by admin on Fri Dec 15 15:21:22 UTC 2023
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PRIMARY | RxNorm | ||
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DB09070
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admin on Fri Dec 15 15:21:22 UTC 2023 , Edited by admin on Fri Dec 15 15:21:22 UTC 2023
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PRIMARY | |||
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TIBOLONE
Created by
admin on Fri Dec 15 15:21:22 UTC 2023 , Edited by admin on Fri Dec 15 15:21:22 UTC 2023
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CHEMBL2103774
Created by
admin on Fri Dec 15 15:21:22 UTC 2023 , Edited by admin on Fri Dec 15 15:21:22 UTC 2023
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759898
Created by
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444008
Created by
admin on Fri Dec 15 15:21:22 UTC 2023 , Edited by admin on Fri Dec 15 15:21:22 UTC 2023
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PRIMARY | |||
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C027385
Created by
admin on Fri Dec 15 15:21:22 UTC 2023 , Edited by admin on Fri Dec 15 15:21:22 UTC 2023
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PRIMARY | |||
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32223
Created by
admin on Fri Dec 15 15:21:22 UTC 2023 , Edited by admin on Fri Dec 15 15:21:22 UTC 2023
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PRIMARY | |||
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SUB11022MIG
Created by
admin on Fri Dec 15 15:21:22 UTC 2023 , Edited by admin on Fri Dec 15 15:21:22 UTC 2023
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PRIMARY | |||
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FF9X0205V2
Created by
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PRIMARY | |||
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100000092534
Created by
admin on Fri Dec 15 15:21:22 UTC 2023 , Edited by admin on Fri Dec 15 15:21:22 UTC 2023
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227-069-1
Created by
admin on Fri Dec 15 15:21:22 UTC 2023 , Edited by admin on Fri Dec 15 15:21:22 UTC 2023
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PRIMARY | |||
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DTXSID5023667
Created by
admin on Fri Dec 15 15:21:22 UTC 2023 , Edited by admin on Fri Dec 15 15:21:22 UTC 2023
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PRIMARY |
Related Record | Type | Details | ||
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TARGET -> AGONIST |
Related Record | Type | Details | ||
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METABOLITE ACTIVE -> PARENT | |||
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METABOLITE ACTIVE -> PARENT | |||
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METABOLITE ACTIVE -> PARENT |
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Related Record | Type | Details | ||
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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Related Record | Type | Details | ||
---|---|---|---|---|
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ACTIVE MOIETY |