Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C24H31F3O4 |
Molecular Weight | 440.4957 |
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](C4=CC(=O)CC[C@]34C)C(F)(F)F
InChI
InChIKey=MXZYUFNILISKBC-WXLIAARGSA-N
InChI=1S/C24H31F3O4/c1-13(28)23(31-14(2)29)10-7-18-16-12-20(24(25,26)27)19-11-15(30)5-8-21(19,3)17(16)6-9-22(18,23)4/h11,16-18,20H,5-10,12H2,1-4H3/t16-,17+,18+,20+,21-,22+,23+/m1/s1
Molecular Formula | C24H31F3O4 |
Molecular Weight | 440.4957 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 7 / 7 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Flumedroxone is a progestative agent. It is a pregnane derivative substituted at C-6 by a trifluoromethyl group. It was tested whether flumedroxone had prophylactic value in migraine. No benefit was found in males, or in females with no history of menstrual exacerbation of migraine. In women whose migraine was worse around the time of menstruation flumedroxone resulted in statistically fewer headaches of less severity. With the dose used in this trial side-effects were frequent, the commonest being polymenorrhagia, which occurred in half the women of reproductive age.
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:13:14 GMT 2023
by
admin
on
Fri Dec 15 15:13:14 GMT 2023
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Record UNII |
S0S93EK936
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Record Status |
Validated (UNII)
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Record Version |
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-
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Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C521
Created by
admin on Fri Dec 15 15:13:14 GMT 2023 , Edited by admin on Fri Dec 15 15:13:14 GMT 2023
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Code System | Code | Type | Description | ||
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C101536
Created by
admin on Fri Dec 15 15:13:14 GMT 2023 , Edited by admin on Fri Dec 15 15:13:14 GMT 2023
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PRIMARY | |||
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3749
Created by
admin on Fri Dec 15 15:13:14 GMT 2023 , Edited by admin on Fri Dec 15 15:13:14 GMT 2023
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192154
Created by
admin on Fri Dec 15 15:13:14 GMT 2023 , Edited by admin on Fri Dec 15 15:13:14 GMT 2023
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PRIMARY | |||
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SUB02211MIG
Created by
admin on Fri Dec 15 15:13:14 GMT 2023 , Edited by admin on Fri Dec 15 15:13:14 GMT 2023
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PRIMARY | |||
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Flumedroxone acetate
Created by
admin on Fri Dec 15 15:13:14 GMT 2023 , Edited by admin on Fri Dec 15 15:13:14 GMT 2023
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PRIMARY | |||
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DTXSID701024795
Created by
admin on Fri Dec 15 15:13:14 GMT 2023 , Edited by admin on Fri Dec 15 15:13:14 GMT 2023
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52412
Created by
admin on Fri Dec 15 15:13:14 GMT 2023 , Edited by admin on Fri Dec 15 15:13:14 GMT 2023
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PRIMARY | |||
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100000086972
Created by
admin on Fri Dec 15 15:13:14 GMT 2023 , Edited by admin on Fri Dec 15 15:13:14 GMT 2023
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PRIMARY | |||
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m189
Created by
admin on Fri Dec 15 15:13:14 GMT 2023 , Edited by admin on Fri Dec 15 15:13:14 GMT 2023
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PRIMARY | Merck Index | ||
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213-577-0
Created by
admin on Fri Dec 15 15:13:14 GMT 2023 , Edited by admin on Fri Dec 15 15:13:14 GMT 2023
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S0S93EK936
Created by
admin on Fri Dec 15 15:13:14 GMT 2023 , Edited by admin on Fri Dec 15 15:13:14 GMT 2023
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PRIMARY | |||
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987-18-8
Created by
admin on Fri Dec 15 15:13:14 GMT 2023 , Edited by admin on Fri Dec 15 15:13:14 GMT 2023
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PRIMARY |
Related Record | Type | Details | ||
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PARENT -> SALT/SOLVATE |
Related Record | Type | Details | ||
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ACTIVE MOIETY |