U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

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
Structure of VILAPRISAN

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

HIDE SMILES / InChI

Molecular Formula C27H29F5O4S
Molecular Weight 544.574
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 5 / 5
E/Z Centers 0
Optical Activity UNSPECIFIED

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

PubMed

PubMed

TitleDatePubMed
Pharmacokinetics and safety of the selective progesterone receptor modulator vilaprisan in healthy postmenopausal women
.
2017 Jan
Vilaprisan for treating uterine fibroids.
2018 May
Patents

Patents

Sample Use Guides

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
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.
Substance Class Chemical
Created
by admin
on Sat Dec 16 08:00:33 GMT 2023
Edited
by admin
on Sat Dec 16 08:00:33 GMT 2023
Record UNII
IN59K53GI9
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
VILAPRISAN
INN   USAN  
INN   USAN  
Official Name English
BAY-1002670
Code English
vilaprisan [INN]
Common Name English
VILAPRISAN [JAN]
Common Name English
20,20,21,21,21-Pentafluoro-17-hydroxy-11β-[4-(methanesulfonyl)phenyl]-19-nor-17α-pregna-4,9-dien-3-one
Systematic Name English
BAY1002670
Code English
19-NORPREGNA-4,9-DIEN-3-ONE, 20,20,21,21,21-PENTAFLUORO-17-HYDROXY-11-(4-(METHYLSULFONYL)PHENYL)-, (11.BETA.,17.ALPHA.)-
Common Name English
VILAPRISAN [USAN]
Common Name English
Vilaprisan [WHO-DD]
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
CAS
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
PUBCHEM
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
USAN
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
EPA CompTox
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
INN
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
WIKIPEDIA
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
SMS_ID
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
DRUG BANK
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
FDA UNII
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
NCI_THESAURUS
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
Related Record Type Details
TARGET->MODULATOR
Related Record Type Details
ACTIVE MOIETY