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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

C[C@]12C[C@H](C3=CC=C(C=C3)S(C)(=O)=O)C4=C5CCC(=O)C=C5CC[C@H]4[C@@H]1CC[C@@]2(O)C(F)(F)C(F)(F)F

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

Description

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.

Originator

Approval Year

PubMed

Patents

Sample Use Guides

In Vivo Use Guide
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
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.