Chemical Structure : LY223982
CAS No.: 117423-74-2
Catalog No.: PC-27538Not For Human Use, Lab Use Only.
LY223982 (CGS23131, SKF107324) is a potent, selective chemotaxin leukotriene B4 (LTB4) receptor with IC50 of 13.2 nM against [3H]LTB4 binding to LTB4 receptor.
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LY223982 (CGS23131, SKF107324) is a potent, selective chemotaxin leukotriene B4 (LTB4) receptor with IC50 of 13.2 nM against [3H]LTB4 binding to LTB4 receptor.
LY223982 blocks LTB4-induced (20 nM) release of formyl peptides (i.e., CHP), LTB4 and C5a with IC50 of 52 nM.
LY223982 is 189-fold more effective in displacing [3H]LTB4 than 35S-N-formyl-L-methionyl-L-leucyl-L-phenylalanine (FMLP) from their corresponding receptors on human neutrophils.
LY223982 is a potent antagonist of the aggregation of human neutrophils by LTB4 with IC50 of 100 nM.
LY223982 inhibits transient leukopenia induced in rabbits with LTB4 (ED50, 3 mg/kg), but not FMLP.
| M.Wt | 502.56 | |
| Formula | C30H30O7 | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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| Chemical Name/SMILES |
(E)-3-(3-(2-Carboxyethyl)-4-((6-(4-methoxyphenyl)hex-5-en-1-yl)oxy)benzoyl)benzoic acid |
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1. Gapinski DM, et al. J Med Chem. 1990 Oct;33(10):2807-13.
2. Moreira-Ludewig R, et al. J Pharmacol Toxicol Methods. 1992 Apr;27(2):95-100.
3. Griswold DE, et al. J Pharmacol Methods. 1991 Jul;25(4):319-28.
4. Jackson WT, et al. J Pharmacol Exp Ther. 1992 Dec;263(3):1009-14.

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