Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C27H29F5O4S |
Molecular Weight | 544.574 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 5 / 5 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@@]12CC[C@@](O)(C(F)(F)C(F)(F)F)[C@@]1(C)C[C@]([H])(C3=CC=C(C=C3)S(C)(=O)=O)C4=C5CCC(=O)C=C5CC[C@@]24[H]
InChI
InChIKey=JUFWQQVHQFDUOD-ANRPBIDPSA-N
InChI=1S/C27H29F5O4S/c1-24-14-21(15-3-7-18(8-4-15)37(2,35)36)23-19-10-6-17(33)13-16(19)5-9-20(23)22(24)11-12-25(24,34)26(28,29)27(30,31)32/h3-4,7-8,13,20-22,34H,5-6,9-12,14H2,1-2H3/t20-,21+,22-,24-,25-/m0/s1
Vilaprisan, a small molecule progesterone receptor antagonist is being developed by Bayer HealthCare Pharmaceuticals (formerly Bayer Schering Pharma) for the treatment of endometriosis and uterine leiomyoma. Hormonal imbalance observed in women with endometriosis is a potential target for treating endometriosis. Vilaprisan is a highly selective steroidal progesterone receptor modulator (SPRM). It is a partial agonist of progesterone receptor, which means that the drug activates progesterone receptors to a certain degree upon binding. This triggers a cascade of biochemical reactions that result in the suppression of prostaglandin production. This, in turn, relieves symptoms such as pain and bleeding. Modulating progesterone by taking vilaprisan might help in treating endometriosis over the long term. Phase I and II studies give encouraging results on the efficacy of vilaprisan at different doses. Like other SPRMs, vilaprisan induces benign changes of endometrium (PR modulator-associated endometrial changes, PAECs). These disappear as treatment is discontinued. Unlike GnRHa treatment, neither UPA nor vilaprisan induce hypoestrogenism and associated symptoms. Phase III studies are ongoing to confirm efficacy and safety of vilaprisan in long-term treatment of symptomatic fibroids.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/27841155
Healthy postmenopausal women received a single oral dose of vilaprisan (1, 5, 15, or 30 mg) and - after a wash-out period - daily doses of the same strength over 28 days.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/23739217
Vilaprisan exhibited strong binding activity to human progesterone receptor (PR) with relative
binding affinity (RBA) of 41+4.8. It showed a strong
antagonistic activity with IC50 values of ca. 0.09 nmol/l with 100% efficacy both at PR-A and PR-B.
Name | Type | Language | ||
---|---|---|---|---|
|
Official Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
NCI_THESAURUS |
C1891
Created by
admin on Sat Dec 16 08:00:33 GMT 2023 , Edited by admin on Sat Dec 16 08:00:33 GMT 2023
|
||
|
NCI_THESAURUS |
C129818
Created by
admin on Sat Dec 16 08:00:33 GMT 2023 , Edited by admin on Sat Dec 16 08:00:33 GMT 2023
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
1262108-14-4
Created by
admin on Sat Dec 16 08:00:33 GMT 2023 , Edited by admin on Sat Dec 16 08:00:33 GMT 2023
|
PRIMARY | |||
|
50915138
Created by
admin on Sat Dec 16 08:00:33 GMT 2023 , Edited by admin on Sat Dec 16 08:00:33 GMT 2023
|
PRIMARY | |||
|
DE-104
Created by
admin on Sat Dec 16 08:00:33 GMT 2023 , Edited by admin on Sat Dec 16 08:00:33 GMT 2023
|
PRIMARY | |||
|
DTXSID201110777
Created by
admin on Sat Dec 16 08:00:33 GMT 2023 , Edited by admin on Sat Dec 16 08:00:33 GMT 2023
|
PRIMARY | |||
|
9725
Created by
admin on Sat Dec 16 08:00:33 GMT 2023 , Edited by admin on Sat Dec 16 08:00:33 GMT 2023
|
PRIMARY | |||
|
Vilaprisan
Created by
admin on Sat Dec 16 08:00:33 GMT 2023 , Edited by admin on Sat Dec 16 08:00:33 GMT 2023
|
PRIMARY | |||
|
100000175837
Created by
admin on Sat Dec 16 08:00:33 GMT 2023 , Edited by admin on Sat Dec 16 08:00:33 GMT 2023
|
PRIMARY | |||
|
DB11971
Created by
admin on Sat Dec 16 08:00:33 GMT 2023 , Edited by admin on Sat Dec 16 08:00:33 GMT 2023
|
PRIMARY | |||
|
IN59K53GI9
Created by
admin on Sat Dec 16 08:00:33 GMT 2023 , Edited by admin on Sat Dec 16 08:00:33 GMT 2023
|
PRIMARY | |||
|
C148505
Created by
admin on Sat Dec 16 08:00:33 GMT 2023 , Edited by admin on Sat Dec 16 08:00:33 GMT 2023
|
PRIMARY |
ACTIVE MOIETY