Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C21H36 |
| Molecular Weight | 288.5105 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 7 / 7 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC[C@H]1CC[C@H]2[C@@H]3CC[C@H]4CCCC[C@]4(C)[C@H]3CC[C@]12C
InChI
InChIKey=JWMFYGXQPXQEEM-GCOKGBOCSA-N
InChI=1S/C21H36/c1-4-15-9-11-18-17-10-8-16-7-5-6-13-20(16,2)19(17)12-14-21(15,18)3/h15-19H,4-14H2,1-3H3/t15-,16+,17-,18-,19-,20-,21+/m0/s1
| Molecular Formula | C21H36 |
| Molecular Weight | 288.5105 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 7 / 7 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Antagonism of neurosteroid modulation of native gamma-aminobutyric acid receptors by (3alpha,5alpha)-17-phenylandrost-16-en-3-ol. | 2007-10-31 |
|
| 3Beta-hydroxysteroids and pregnenolone sulfate inhibit recombinant rat GABA(A) receptor through different channel property. | 2007-02-28 |
|
| Progesterone metabolites in breast cancer. | 2006-09 |
|
| The role of progesterone metabolites in breast cancer: potential for new diagnostics and therapeutics. | 2005-02 |
|
| Thymol, a constituent of thyme essential oil, is a positive allosteric modulator of human GABA(A) receptors and a homo-oligomeric GABA receptor from Drosophila melanogaster. | 2003-12 |
|
| Changes in 5alpha-pregnane steroids and neurosteroidogenic enzyme expression in fetal sheep with umbilicoplacental embolization. | 2003-12 |
|
| Changes in 5alpha-pregnane steroids and neurosteroidogenic enzyme expression in the perinatal sheep. | 2003-06 |
|
| Neuroactive steroids: mechanisms of action and neuropsychopharmacological properties. | 2003-02 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:55:28 GMT 2025
by
admin
on
Mon Mar 31 21:55:28 GMT 2025
|
| Record UNII |
ZTF5KN7S9R
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
DTXSID201031678
Created by
admin on Mon Mar 31 21:55:28 GMT 2025 , Edited by admin on Mon Mar 31 21:55:28 GMT 2025
|
PRIMARY | |||
|
6857463
Created by
admin on Mon Mar 31 21:55:28 GMT 2025 , Edited by admin on Mon Mar 31 21:55:28 GMT 2025
|
PRIMARY | |||
|
641-85-0
Created by
admin on Mon Mar 31 21:55:28 GMT 2025 , Edited by admin on Mon Mar 31 21:55:28 GMT 2025
|
PRIMARY | |||
|
m1528
Created by
admin on Mon Mar 31 21:55:28 GMT 2025 , Edited by admin on Mon Mar 31 21:55:28 GMT 2025
|
PRIMARY | Merck Index | ||
|
211-378-3
Created by
admin on Mon Mar 31 21:55:28 GMT 2025 , Edited by admin on Mon Mar 31 21:55:28 GMT 2025
|
PRIMARY | |||
|
Allopregnane
Created by
admin on Mon Mar 31 21:55:28 GMT 2025 , Edited by admin on Mon Mar 31 21:55:28 GMT 2025
|
PRIMARY | |||
|
ZTF5KN7S9R
Created by
admin on Mon Mar 31 21:55:28 GMT 2025 , Edited by admin on Mon Mar 31 21:55:28 GMT 2025
|
PRIMARY | |||
|
20656
Created by
admin on Mon Mar 31 21:55:28 GMT 2025 , Edited by admin on Mon Mar 31 21:55:28 GMT 2025
|
PRIMARY |