Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C21H29FO2 |
| Molecular Weight | 332.4522 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 6 / 6 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@@]12CC[C@H](C(=O)CF)[C@@]1(C)CC[C@@]3([H])[C@@]2([H])CCC4=CC(=O)CC[C@]34C
InChI
InChIKey=NWJJZHDRVSKTBB-YFWFAHHUSA-N
InChI=1S/C21H29FO2/c1-20-9-7-14(23)11-13(20)3-4-15-16-5-6-18(19(24)12-22)21(16,2)10-8-17(15)20/h11,15-18H,3-10,12H2,1-2H3/t15-,16-,17-,18+,20-,21-/m0/s1
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Synthesis of fluorine-18 labeled 21-fluoroprogesterone. | 1977 Oct |
|
| The effect of progesterone analogues, naturally occurring steroids, and contraceptive progestins on hypothalamic and anterior pituitary delta4-steroid (progesterone) 5alpha-reductase. | 1978 Jun |
|
| Steroid binding specificity of the hamster uterine progesterone receptor. | 1980 Jun |
Patents
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DTXSID00963005
Created by
admin on Sat Dec 16 08:24:58 GMT 2023 , Edited by admin on Sat Dec 16 08:24:58 GMT 2023
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434-18-4
Created by
admin on Sat Dec 16 08:24:58 GMT 2023 , Edited by admin on Sat Dec 16 08:24:58 GMT 2023
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19608
Created by
admin on Sat Dec 16 08:24:58 GMT 2023 , Edited by admin on Sat Dec 16 08:24:58 GMT 2023
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200138
Created by
admin on Sat Dec 16 08:24:58 GMT 2023 , Edited by admin on Sat Dec 16 08:24:58 GMT 2023
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DX31XG2JO0
Created by
admin on Sat Dec 16 08:24:58 GMT 2023 , Edited by admin on Sat Dec 16 08:24:58 GMT 2023
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PRIMARY |
SUBSTANCE RECORD
