Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C23H36N2O2 |
Molecular Weight | 372.5441 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 7 / 7 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@@]12CC[C@H](C(=O)NC(C)(C)C)[C@@]1(C)CC[C@@]3([H])[C@@]2([H])CC[C@@]4([H])NC(=O)C=C[C@]34C
InChI
InChIKey=DBEPLOCGEIEOCV-WSBQPABSSA-N
InChI=1S/C23H36N2O2/c1-21(2,3)25-20(27)17-8-7-15-14-6-9-18-23(5,13-11-19(26)24-18)16(14)10-12-22(15,17)4/h11,13-18H,6-10,12H2,1-5H3,(H,24,26)(H,25,27)/t14-,15-,16-,17+,18+,22-,23+/m0/s1
Molecular Formula | C23H36N2O2 |
Molecular Weight | 372.5441 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 7 / 7 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:06:54 UTC 2023
by
admin
on
Fri Dec 15 15:06:54 UTC 2023
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Record UNII |
57GNO57U7G
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Record Status |
Validated (UNII)
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Record Version |
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-
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Common Name | English |
Classification Tree | Code System | Code | ||
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WHO-VATC |
QG04CB01
Created by
admin on Fri Dec 15 15:06:54 UTC 2023 , Edited by admin on Fri Dec 15 15:06:54 UTC 2023
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EPA PESTICIDE CODE |
129113
Created by
admin on Fri Dec 15 15:06:54 UTC 2023 , Edited by admin on Fri Dec 15 15:06:54 UTC 2023
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NCI_THESAURUS |
C2319
Created by
admin on Fri Dec 15 15:06:54 UTC 2023 , Edited by admin on Fri Dec 15 15:06:54 UTC 2023
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WHO-ATC |
G04CA51
Created by
admin on Fri Dec 15 15:06:54 UTC 2023 , Edited by admin on Fri Dec 15 15:06:54 UTC 2023
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WHO-ATC |
G04CB01
Created by
admin on Fri Dec 15 15:06:54 UTC 2023 , Edited by admin on Fri Dec 15 15:06:54 UTC 2023
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WHO-VATC |
QD11AX10
Created by
admin on Fri Dec 15 15:06:54 UTC 2023 , Edited by admin on Fri Dec 15 15:06:54 UTC 2023
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NDF-RT |
N0000000126
Created by
admin on Fri Dec 15 15:06:54 UTC 2023 , Edited by admin on Fri Dec 15 15:06:54 UTC 2023
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LIVERTOX |
NBK548319
Created by
admin on Fri Dec 15 15:06:54 UTC 2023 , Edited by admin on Fri Dec 15 15:06:54 UTC 2023
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WHO-ATC |
D11AX10
Created by
admin on Fri Dec 15 15:06:54 UTC 2023 , Edited by admin on Fri Dec 15 15:06:54 UTC 2023
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WHO-VATC |
QG04CA51
Created by
admin on Fri Dec 15 15:06:54 UTC 2023 , Edited by admin on Fri Dec 15 15:06:54 UTC 2023
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NDF-RT |
N0000175836
Created by
admin on Fri Dec 15 15:06:54 UTC 2023 , Edited by admin on Fri Dec 15 15:06:54 UTC 2023
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Code System | Code | Type | Description | ||
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57GNO57U7G
Created by
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6818
Created by
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PRIMARY | |||
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CHEMBL710
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57363
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DB01216
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759318
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PRIMARY | |||
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100000092656
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C1099
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FINASTERIDE
Created by
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741485
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PRIMARY | |||
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25025
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admin on Fri Dec 15 15:06:54 UTC 2023 , Edited by admin on Fri Dec 15 15:06:54 UTC 2023
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PRIMARY | RxNorm | ||
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57GNO57U7G
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DTXSID3020625
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D018120
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1270402
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PRIMARY | |||
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98319-26-7
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m5383
Created by
admin on Fri Dec 15 15:06:54 UTC 2023 , Edited by admin on Fri Dec 15 15:06:54 UTC 2023
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PRIMARY | Merck Index | ||
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5062
Created by
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6793
Created by
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1171
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6539
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AA-52
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SUB07629MIG
Created by
admin on Fri Dec 15 15:06:54 UTC 2023 , Edited by admin on Fri Dec 15 15:06:54 UTC 2023
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PRIMARY |
Related Record | Type | Details | ||
---|---|---|---|---|
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TARGET->WEAK INHIBITOR |
IC50
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TARGET -> INHIBITOR |
A Slow-Binding 5a-Reductase Inhibitor
TIME-DEPENDENT INHIBITION
IC50
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Related Record | Type | Details | ||
---|---|---|---|---|
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METABOLITE -> PARENT |
IN DOGS
FECAL; PLASMA; URINE
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METABOLITE LESS ACTIVE -> PARENT |
via the cytochrome P450 3A4 enzyme subfamily
MAJOR
URINE
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METABOLITE LESS ACTIVE -> PARENT |
via the cytochrome P450 3A4 enzyme subfamily
MAJOR
PLASMA
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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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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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Related Record | Type | Details | ||
---|---|---|---|---|
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ACTIVE MOIETY |
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