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GPCR/G Protein
Leukotriene Receptor

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Leukotriene Receptor

Chemical Structure Cat. No. Product Name CAS No.
SC 57461A Chemical Structure
BCP36043 SC 57461A 423169-68-0
SC 57461A is a potent and competitive inhibitor of recombinant human leukotriene A4 hydrolase in vitro.
LYS-006 Chemical Structure
BCP35741 LYS-006 1799681-85-8
LYS-006 is a novel leukotriene A4 hydrolase inhibitor.
11-Keto-beta-boswellic acid Chemical Structure
BCP32934 11-Keto-beta-boswellic acid 17019-92-0
11-Keto-beta-boswellic acid is a pentacyclic triterpenic acid of the oleogum resin from the bark of the Boswellia serrate tree, popularly known as Indian Frankincense.
Cilastatin Chemical Structure
BCP21135 Cilastatin 82009-34-5
Cilastatin is a Renal Dehydropeptidase Inhibitor. The mechanism of action of cilastatin is as a Dipeptidase Inhibitor.
Montelukast Chemical Structure
BCP28542 Montelukast 158966-92-8
Montelukast is a Leukotriene Receptor Antagonist. The mechanism of action of montelukast is as a Leukotriene Receptor Antagonist.
Montelukast Sulfone Chemical Structure
BCP27889 Montelukast Sulfone 1266620-74-9
Montelukast Sulfone is an impurity of Montelukast Sodium.
Tipelukast Chemical Structure
BCP17000 Tipelukast 125961-82-2
Tipelukast is a sulfidopeptide leukotriene receptor antagonist, an orally bioavailable anti-inflammatory agent and used for the treatment of asthma.
CP-105696 Chemical Structure
BCP30009 CP-105696 158081-99-3
CP-105696 is a potent and selective Leukotriene B4 Receptor antagonist, with an IC50 of 8.42 nM.
L-660711 Chemical Structure
BCP30001 L-660711 135028-15-8
MK-571 is a selective, orally active CysLT1 receptor antagonist. It blocks the binding of LTD4, but not LTC4, to human and guinea pig lung membranes with Ki values of 0.22 nM and 2.1 nM, respectively. MK-571 attenuates kidney ischemia and reperfusion-induced airway hypersensitivity in rats. MK-571 alters bronchoalveolar lavage fluid proteome in a mouse asthma model.
Etalocib Chemical Structure
BCP29555 Etalocib 161172-51-6
Etalocib, also known as LY293111 and VML295, is a novel diaryl ether carboxylic acid derivative, is a potent and selective inhibitor of the lipoxygenase pathway either directly through 5'-lipoxygenase or via antagonism of the leukotriene B4 (LTB4) receptor.
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