Bioactivity:

Verlukast is an (R)-enantiomer of MK-571 and a potent and selective LTD4 receptor antagonist. Verlukast showed [3H]leukotriene D4 binding in guinea-pig (IC50 = 3.1 +/- 0.5 nM) and human (IC50 = 8.0 +/- 3.0 nM) lung homogenates and dimethyl sulfoxide diffe

CAS nr:

120443-16-5

Purity:

98%

Molecular Weight:

515,08

SMILES:

O=C(O)CCS[C@H](C1=CC=CC(/C=C/C2=NC3=CC(Cl)=CC=C3C=C2)=C1)SCCC(N(C)C)=O

Formula:

C26H27ClN2O3S2

Pathway:

Target: