Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C18H18N2O |
| Molecular Weight | 278.3483 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Charge | 0 |
| Stereo Comments | Meso |
SHOW SMILES / InChI
SMILES
O[C@@H]1C[C@@H]2CC[C@H](C1)N2C3=C4C=CC=CC4=C(C=C3)C#N
InChI
InChIKey=ATKWLNSCJYLXPF-FICVDOATSA-N
InChI=1S/C18H18N2O/c19-11-12-5-8-18(17-4-2-1-3-16(12)17)20-13-6-7-14(20)10-15(21)9-13/h1-5,8,13-15,21H,6-7,9-10H2/t13-,14+,15+
| Molecular Formula | C18H18N2O |
| Molecular Weight | 278.3483 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:35:17 GMT 2025
by
admin
on
Mon Mar 31 22:35:17 GMT 2025
|
| Record UNII |
U8VS41J5O6
|
| Record Status |
Validated (UNII)
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| Record Version |
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-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
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Common Name | English | ||
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Preferred Name | English | ||
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Systematic Name | English | ||
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Systematic Name | English |
| Classification Tree | Code System | Code | ||
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WIKIPEDIA |
Designer-drugs-AC-262536
Created by
admin on Mon Mar 31 22:35:17 GMT 2025 , Edited by admin on Mon Mar 31 22:35:17 GMT 2025
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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U8VS41J5O6
Created by
admin on Mon Mar 31 22:35:17 GMT 2025 , Edited by admin on Mon Mar 31 22:35:17 GMT 2025
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PRIMARY | |||
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870888-46-3
Created by
admin on Mon Mar 31 22:35:17 GMT 2025 , Edited by admin on Mon Mar 31 22:35:17 GMT 2025
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PRIMARY | |||
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DTXSID701336168
Created by
admin on Mon Mar 31 22:35:17 GMT 2025 , Edited by admin on Mon Mar 31 22:35:17 GMT 2025
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PRIMARY | |||
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44512434
Created by
admin on Mon Mar 31 22:35:17 GMT 2025 , Edited by admin on Mon Mar 31 22:35:17 GMT 2025
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PRIMARY | |||
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AC-262,536
Created by
admin on Mon Mar 31 22:35:17 GMT 2025 , Edited by admin on Mon Mar 31 22:35:17 GMT 2025
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PRIMARY | AC-262,356 is a drug developed by Acadia Pharmaceuticals which acts as a selective androgen receptor modulator. Chemically it possesses endo-exo isomerism, with the endo form being the active form. It acts as a partial agonist for the androgen receptor with a Ki of 5nM, and no significant affinity for any other receptors tested. In animal studies it produced a maximal effect of around 66% of the anabolic action of testosterone, but only around 27% of its potency as an androgen. | ||
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DB13935
Created by
admin on Mon Mar 31 22:35:17 GMT 2025 , Edited by admin on Mon Mar 31 22:35:17 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
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ACTIVE MOIETY |
