Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C19H28O3 |
| Molecular Weight | 304.4238 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 6 / 6 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@]12CC[C@H]3[C@@H](CCC4=C(O)C(=O)CC[C@]34C)[C@@H]1CC[C@@H]2O
InChI
InChIKey=BQOIJSIMMIDHMO-FBPKJDBXSA-N
InChI=1S/C19H28O3/c1-18-10-8-15(20)17(22)14(18)4-3-11-12-5-6-16(21)19(12,2)9-7-13(11)18/h11-13,16,21-22H,3-10H2,1-2H3/t11-,12-,13-,16-,18+,19-/m0/s1
| Molecular Formula | C19H28O3 |
| Molecular Weight | 304.4238 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 6 / 6 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Synthesis and steroid sulphatase inhibitory activity of C19- and C21-steroidal derivatives bearing a benzyl-inhibiting group. | 2001-10-16 |
|
| The aryl hydrocarbon receptor (AHR)/AHR nuclear translocator (ARNT) heterodimer interacts with naturally occurring estrogen response elements. | 1999-11-25 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:15:51 GMT 2025
by
admin
on
Mon Mar 31 22:15:51 GMT 2025
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| Record UNII |
912GOZ167T
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| Record Status |
Validated (UNII)
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| Record Version |
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Preferred Name | English | ||
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Common Name | English | ||
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| Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C2017
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DEA NO. |
4000
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160615
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DTXSID80902477
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2141-17-5
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4-HYDROXYTESTOSTERONE
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912GOZ167T
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DB01485
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C113835
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admin on Mon Mar 31 22:15:51 GMT 2025 , Edited by admin on Mon Mar 31 22:15:51 GMT 2025
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PRIMARY | NCIT |
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ACTIVE MOIETY |
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