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Description: Sitaxentan sodium (also known as Sitaxsentan, TBC-11251 and IPI 1040) is a selective and orally bioavailable endothelin A receptor (ETA) antagonist with IC50 and Ki of 1.4 nM and 0.43 nM, respectively, it exhibits 7000-fold selectivity over ETB. Sitaxentanis a medication for the treatment of pulmonary arterial hypertension (PAH). Sitaxentan is a small molecule that blocks the action of endothelin (ET) on the endothelin-A (ETA) receptor selectively (by a factor of 6000 compared with the ETB).
References: J Med Chem. 1997; 40(11):1690-7; Pulm Pharmacol Ther. 2000; 13(2):87-97; Neurosurgery. 1998; 43(6):1409-17.
Related CAS: 210421-74-2 (sodium salt); 184036-34-8 (free)
Name: sodium (4-chloro-3-methylisoxazol-5-yl)((2-(2-(6-methylbenzo[d][1, 3]dioxol-5-yl)acetyl)thiophen-3-yl)sulfonyl)amide
InChi Key: MDTNUYUCUYPIHE-UHFFFAOYSA-N
InChi Code: InChI=1S/C18H14ClN2O6S2.Na/c1-9-5-13-14(26-8-25-13)7-11(9)6-12(22)17-15(3-4-28-17)29(23, 24)21-18-16(19)10(2)20-27-18; /h3-5, 7H, 6, 8H2, 1-2H3; /q-1; +1
SMILES Code: O=C(C(SC=C1)=C1S(N([Na])C2=C(C(C)=NO2)Cl)(=O)=O)CC3=C(C)C=C(OCO4)C4=C3
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