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InChi: InChI=1S/C20H17ClF4N4O4S/c21-14-3-5-15(6-4-14)34(31
25(12):1883-90
Smiles: FC1=CC=C(Cl)C=C1C1N=C2N=CC=NC2=C(NC2C=CN=CC=2)N=1
¹⁵]hexadeca-1(15)
¹⁶]hexadeca-1(15)
(R)-Elagolix Size:Contact [email protected] for quotation InChi: InChI=1S/C20H17ClF4N4O4S/c21-14-3-5-15(6-4-14)34(31Elagolix is a highly potent, selective, orally active, short duration, non peptide antagonist of the gonadotropin releasing hormone receptor (GnRHR) (KD = 54 pM). Target: GnRHin vitro: Elagolix is a short acting, nonpeptide, GnRH antagonist, administered orally, that unlike injectable depot GnRH agonists and antagonists, produces a dose dependent suppression of ovarian estrogen production, that is, from partial suppression at lower doses to full
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