Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C24H36O3 |
| Molecular Weight | 372.5408 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 7 / 7 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@@]12CC[C@](OC(C)=O)(C(C)=O)[C@@]1(C)CC[C@@]3([H])[C@@]2([H])C[C@H](C)C4=CCCC[C@]34C
InChI
InChIKey=KDLNOQQQEBKBQM-DICPTYMLSA-N
InChI=1S/C24H36O3/c1-15-14-18-20(22(4)11-7-6-8-19(15)22)9-12-23(5)21(18)10-13-24(23,16(2)25)27-17(3)26/h8,15,18,20-21H,6-7,9-14H2,1-5H3/t15-,18+,20-,21-,22-,23-,24-/m0/s1
Anagestone acetate is a progestin medication, used in the 1960s in combination with the estrogen mestranol as a combined birth control pill. Toxicological study of chronic administration in dogs and monkeys showed the increased risk of developing malignant tumors in the mammary glands and a dose-dependent, nonprogressive decrease in hemoglobin and hematocrits. The drug was voluntarily withdrawn from the market in 1969.
Approval Year
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| Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C776
Created by
admin on Fri Dec 15 15:00:05 GMT 2023 , Edited by admin on Fri Dec 15 15:00:05 GMT 2023
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| Code System | Code | Type | Description | ||
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C76302
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DTXSID50953411
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208
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CHEMBL2104489
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221-535-8
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3137-73-3
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Anagestone acetate
Created by
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252301
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SUB00522MIG
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m563
Created by
admin on Fri Dec 15 15:00:05 GMT 2023 , Edited by admin on Fri Dec 15 15:00:05 GMT 2023
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PRIMARY | Merck Index | ||
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GNT396G9QT
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73880
Created by
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100000085181
Created by
admin on Fri Dec 15 15:00:05 GMT 2023 , Edited by admin on Fri Dec 15 15:00:05 GMT 2023
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PRIMARY |
ACTIVE MOIETY
SUBSTANCE RECORD
