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HAMI3379

Chemical Structure : HAMI3379

CAS No.: 1245653-57-9

HAMI3379 (HAMI 3379;HAMI-3379)

Catalog No.: PC-35285Not For Human Use, Lab Use Only.

HAMI3379 (HAMI-3379) is a potent and selective antagonist of cysteinyl leukotriene 2 (CysLT(2)) receptor, inhibits LTD4- and LTC4-induced intracellular calcium mobilization withIC50 of 3.8 nM and 4.4 nM respectively.

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Purity & Documentation Purity: >98% (HPLC)

Biological Activity

HAMI3379 (HAMI-3379) is a potent and selective antagonist of cysteinyl leukotriene 2 (CysLT(2)) receptor, inhibits LTD4- and LTC4-induced intracellular calcium mobilization withIC50 of 3.8 nM and 4.4 nM respectively; exhibits very low potency on a recombinant CysLT(1) receptors (IC50>10 uM), does not exhibit any agonistic activity on both CysLT receptors; concentration-dependently inhibits and reverses the LTC(4)-induced perfusion pressure increase and contractility decrease in isolated Langendorff-perfused guinea pig hearts, protects against acute brain injury after focal cerebral ischemia in rats.

Physicochemical Properties

M.Wt 595.733
Formula C34H45NO8
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

3-({[(1S,3S)-3-carboxycyclohexyl]amino}carbonyl)-4-(3-{4-[4-(cyclo-hexyloxy)butoxy]phenyl}propoxy) benzoic acid

References

1. Merten N, et al. Cell Chem Biol. 2018 Jun 21;25(6):775-786.e5.

2. Wunder F, et al. Br J Pharmacol. 2010 May;160(2):399-409.

3. Shi QJ, et al. Brain Res. 2012 Nov 12;1484:57-67.

4. Zhang XY, et al. J Pharmacol Exp Ther. 2013 Aug;346(2):328-41.

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