Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C22H34O2 |
| Molecular Weight | 330.5042 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 7 / 7 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@@]12CC[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=GAIHSQSRHYQICG-DACBVQKSSA-N
InChI=1S/C22H34O2/c1-14-13-16-18(20(3)10-6-5-7-17(14)20)8-11-21(4)19(16)9-12-22(21,24)15(2)23/h7,14,16,18-19,24H,5-6,8-13H2,1-4H3/t14-,16+,18-,19-,20-,21-,22-/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 The drug was voluntarily withdrawn from the market in 1969.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 16:15:28 GMT 2023 , Edited by admin on Fri Dec 15 16:15:28 GMT 2023
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| Code System | Code | Type | Description | ||
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SUB05498MIG
Created by
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2740-52-5
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1974
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100000086919
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CHEMBL2104489
Created by
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C79752
Created by
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DTXSID001043405
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S8FB38IU3G
Created by
admin on Fri Dec 15 16:15:28 GMT 2023 , Edited by admin on Fri Dec 15 16:15:28 GMT 2023
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Anagestone
Created by
admin on Fri Dec 15 16:15:28 GMT 2023 , Edited by admin on Fri Dec 15 16:15:28 GMT 2023
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C017235
Created by
admin on Fri Dec 15 16:15:28 GMT 2023 , Edited by admin on Fri Dec 15 16:15:28 GMT 2023
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m563
Created by
admin on Fri Dec 15 16:15:28 GMT 2023 , Edited by admin on Fri Dec 15 16:15:28 GMT 2023
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PRIMARY | Merck Index | ||
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160650
Created by
admin on Fri Dec 15 16:15:28 GMT 2023 , Edited by admin on Fri Dec 15 16:15:28 GMT 2023
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PRIMARY |
ACTIVE MOIETY
