Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C28H35NO3 |
Molecular Weight | 433.5824 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 5 / 5 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@@]12CC[C@](O)(C(C)=O)[C@@]1(C)C[C@]([H])(C3=CC=C(C=C3)N(C)C)C4=C5CCC(=O)C=C5CC[C@@]24[H]
InChI
InChIKey=HKDLNTKNLJPAIY-WKWWZUSTSA-N
InChI=1S/C28H35NO3/c1-17(30)28(32)14-13-25-23-11-7-19-15-21(31)10-12-22(19)26(23)24(16-27(25,28)2)18-5-8-20(9-6-18)29(3)4/h5-6,8-9,15,23-25,32H,7,10-14,16H2,1-4H3/t23-,24+,25-,27-,28-/m0/s1
Molecular Formula | C28H35NO3 |
Molecular Weight | 433.5824 |
Charge | 0 |
Count |
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Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 5 / 5 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 17:17:44 UTC 2023
by
admin
on
Fri Dec 15 17:17:44 UTC 2023
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Record UNII |
6J5J15Q2X8
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Record Status |
Validated (UNII)
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Record Version |
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-
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Official Name | English | ||
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Common Name | English | ||
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Common Name | English | ||
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Common Name | English | ||
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Common Name | English | ||
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Common Name | English | ||
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Common Name | English | ||
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Common Name | English |
Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C1891
Created by
admin on Fri Dec 15 17:17:44 UTC 2023 , Edited by admin on Fri Dec 15 17:17:44 UTC 2023
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WHO-ATC |
G03XB02
Created by
admin on Fri Dec 15 17:17:44 UTC 2023 , Edited by admin on Fri Dec 15 17:17:44 UTC 2023
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WHO-VATC |
QG03XB02
Created by
admin on Fri Dec 15 17:17:44 UTC 2023 , Edited by admin on Fri Dec 15 17:17:44 UTC 2023
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WHO-ATC |
G03AD02
Created by
admin on Fri Dec 15 17:17:44 UTC 2023 , Edited by admin on Fri Dec 15 17:17:44 UTC 2023
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WHO-VATC |
QG03AD02
Created by
admin on Fri Dec 15 17:17:44 UTC 2023 , Edited by admin on Fri Dec 15 17:17:44 UTC 2023
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NDF-RT |
N0000191263
Created by
admin on Fri Dec 15 17:17:44 UTC 2023 , Edited by admin on Fri Dec 15 17:17:44 UTC 2023
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Code System | Code | Type | Description | ||
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SUB30471
Created by
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PRIMARY | |||
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4166
Created by
admin on Fri Dec 15 17:17:44 UTC 2023 , Edited by admin on Fri Dec 15 17:17:44 UTC 2023
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PRIMARY | |||
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6J5J15Q2X8
Created by
admin on Fri Dec 15 17:17:44 UTC 2023 , Edited by admin on Fri Dec 15 17:17:44 UTC 2023
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PRIMARY | |||
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6J5J15Q2X8
Created by
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PRIMARY | |||
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DB08867
Created by
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PRIMARY | |||
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159811-51-5
Created by
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PRIMARY | |||
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DTXSID501025842
Created by
admin on Fri Dec 15 17:17:44 UTC 2023 , Edited by admin on Fri Dec 15 17:17:44 UTC 2023
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PRIMARY | |||
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m11300
Created by
admin on Fri Dec 15 17:17:44 UTC 2023 , Edited by admin on Fri Dec 15 17:17:44 UTC 2023
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PRIMARY | Merck Index | ||
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C91056
Created by
admin on Fri Dec 15 17:17:44 UTC 2023 , Edited by admin on Fri Dec 15 17:17:44 UTC 2023
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PRIMARY | |||
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C094854
Created by
admin on Fri Dec 15 17:17:44 UTC 2023 , Edited by admin on Fri Dec 15 17:17:44 UTC 2023
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PRIMARY | |||
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1005921
Created by
admin on Fri Dec 15 17:17:44 UTC 2023 , Edited by admin on Fri Dec 15 17:17:44 UTC 2023
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PRIMARY | RxNorm | ||
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13559281
Created by
admin on Fri Dec 15 17:17:44 UTC 2023 , Edited by admin on Fri Dec 15 17:17:44 UTC 2023
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PRIMARY | |||
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Ulipristal
Created by
admin on Fri Dec 15 17:17:44 UTC 2023 , Edited by admin on Fri Dec 15 17:17:44 UTC 2023
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PRIMARY | |||
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N0000191262
Created by
admin on Fri Dec 15 17:17:44 UTC 2023 , Edited by admin on Fri Dec 15 17:17:44 UTC 2023
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PRIMARY | Selective Progesterone Receptor Modulators [MoA] | ||
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CHEMBL2103846
Created by
admin on Fri Dec 15 17:17:44 UTC 2023 , Edited by admin on Fri Dec 15 17:17:44 UTC 2023
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PRIMARY | |||
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100000093430
Created by
admin on Fri Dec 15 17:17:44 UTC 2023 , Edited by admin on Fri Dec 15 17:17:44 UTC 2023
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PRIMARY | |||
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8367
Created by
admin on Fri Dec 15 17:17:44 UTC 2023 , Edited by admin on Fri Dec 15 17:17:44 UTC 2023
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PRIMARY | |||
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WW-157
Created by
admin on Fri Dec 15 17:17:44 UTC 2023 , Edited by admin on Fri Dec 15 17:17:44 UTC 2023
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PRIMARY |
Related Record | Type | Details | ||
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BINDER->LIGAND |
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TARGET -> AGONIST |
Ulipristal acetate is an orally-active progesterone agonist/antagonist with antagonistic and partial agonistic effects at the progesterone receptor.
BINDING
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BINDER->LIGAND |
BINDING
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METABOLIC ENZYME -> SUBSTRATE |
Concomitant administration of CYP3A4 inhibitors may inhibit the metabolism of ulipristal acetate and cause increased plasma concentration of ulipristal acetate. In addition, concomitant administration of CYP3A4 inducers may reduce plasma concentrations of ulipristal acetate and may result in decrease in efficacy.
MAJOR
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TARGET -> INHIBITOR |
Related Record | Type | Details | ||
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ACTIVE MOIETY |
Name | Property Type | Amount | Referenced Substance | Defining | Parameters | References |
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Biological Half-life | PHARMACOKINETIC |
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Tmax | PHARMACOKINETIC |
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oral administration |
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