Tanaproget is an orally effective, selective nonsteroidal progesterone receptor (PR) agonist targeting human PR with an IC50 of 1.7 nM. Tanaproget promotes the interaction between PR receptors and coactivators (such as SRC-1), thereby inhibiting the secretion of matrix metalloproteinases (MMP-3/MMP-7) and reducing endometrial tissue invasion and angiogenesis. Tanaproget can be used for contraception and endometriosis inhibition research[1][2][3].
Molekulargewicht:
297.37
Reinheit:
99.73
CAS Nummer:
[304853-42-7]
Formel:
C16H15N3OS
Target-Kategorie:
Progesterone Receptor
Anwendungsbeschreibung:
MCE Product type: Reference compound
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