| Identification | Back Directory | [Name]
Ro 46-8443 | [CAS]
175556-12-4 | [Synonyms]
Ro 46-8443
RO46-8443, CID 5312146
4-TERT-BUTYL-N-[6-[(2R)-2,3-DIHYDROXYPROPOXY]-5-(2-METHOXYPHENOXY)-2-(4-METHOXYPHENYL)PYRIMIDIN-4-YL]BENZENESULFONAMIDE
(R)-4-(tert-Butyl)-N-(6-(2,3-dihydroxypropoxy)-5-(2-methoxyphenoxy)-2-(4-methoxyphenyl)pyrimidin-4-yl)benzenesulfonamide
Inhibitor,RO 468443,Ro 46-8443,selective,ETB,normotensive,RO 46 8443,inhibit,Endothelin Receptor,hypertensive rats,non-peptide
(R)-N-[6-(2,3-Dihydroxypropoxy)-5-(2-methoxyphenoxy)-2-(4-methoxyphenyl)-4-pyrimidinyl]-4-(1,1-dimethylethyl)benzenesulfonamide
Benzenesulfonamide, N-[6-[(2R)-2,3-dihydroxypropoxy]-5-(2-methoxyphenoxy)-2-(4-methoxyphenyl)-4-pyrimidinyl]-4-(1,1-dimethylethyl)- | [EINECS(EC#)]
604-604-1 | [Molecular Formula]
C31H35N3O8S | [MDL Number]
MFCD00946586 | [MOL File]
175556-12-4.mol | [Molecular Weight]
609.69 |
| Hazard Information | Back Directory | [Uses]
Ro 46-8443 is the first non-peptide endothelin ETB receptor selective antagonist. Ro 46-8443 displays an at least 100-fold selectivity for ETB (IC50: 34-69 nM) over ETA receptors (IC50: 6800 nM)[1][2]. | [IC 50]
ETB: 34-69 nM (IC50); ETA: 6800 nM (IC50) | [References]
[1] Breu V, et al. In vitro characterisation of Ro 46-8443, the first non-peptide antagonist selective for the endothelin ETB receptor. FEBS Lett. 1996;383(1-2):37-41. DOI:10.1016/0014-5793(96)00213-x
[2] Clozel M, et al. The role of ETB receptors in normotensive and hypertensive rats as revealed by the non-peptide selective ETB receptor antagonist Ro 46-8443. FEBS Lett. 1996;383(1-2):42-45. DOI:10.1016/0014-5793(96)00212-8 |
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