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| Product | Description | |
|---|---|---|
| Verlukast | A receptor antagonist for the treatment of respiratory diseases. Group: Biochemicals. Alternative Names: 3- [ [ (R) - [3- [ (1E) -2- (7-Chloro-2-quinolinyl) ethenyl] phenyl] [ [3- (dimethylamino) -3-oxopropyl] thio] methyl] thio] -propanoic Acid; L 668019; MK 679; R-(-)-MK 571. Grades: Highly Purified. CAS No. 120443-16-5. Pack Sizes: 5mg, 10mg. US Biological Life Sciences. |  Worldwide |
| Verlukast | This active molecular is a R-enantiomer of MK-571 which is a selective LTD4 receptor antagonist. Verlukast showed [3H]leukotriene D4 binding in guinea-pig with IC50 value of 3.1+/-0.5nM, in human lung homogenates with IC50 value of 8.0+/-3.0nM and in dimethyl sulfoxide differentiated U937 cell membrane preparations with IC50 value of 10.7+/-1.6nM. Verlukast was in clinical development for the treatment of respiratory diseases but was discontinued for treatment of Asthma. Uses: The treatment of respiratory diseases. Synonyms: 3-[[(R)-[3-[(1E)-2-(7-Chloro-2-quinolinyl)ethenyl]phenyl][[3-(dimethylamino)-3-oxopropyl]thio]methyl]thio]-propanoic Acid; L 668,019; L 668019; L-668,019; MK 0679; MK 679; MK-679; R-(-)-MK 571. Grades: 95%. CAS No. 120443-16-5. Molecular formula: C26H27ClN2O3S2. Mole weight: 515.09. |  |
| Verlukast-d6 | A receptor antagonist for the treatment of respiratory diseases. Group: Biochemicals. Alternative Names: 3- [ [ (R) - [3- [ (1E) -2- (7-Chloro-2-quinolinyl) ethenyl] phenyl] [ [3- (di (methyl-d3) amino) -3-oxopropyl] thio] methyl] thio] -propanoic Acid; L 668019-d6; MK 679-d6; R-(-)-MK 571-d6. Grades: Highly Purified. CAS No. 153698-86-3. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
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