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LY 163443

Catalog No. T27877   CAS 97581-70-9
Synonyms: LY163443, LY-163443

LY 163443 is an dual receptor antagonist of LTD4 and LTE4.

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LY 163443 Chemical Structure
LY 163443, CAS 97581-70-9
Pack Size Availability Price/USD Quantity
25 mg 6-8 weeks $ 1,670.00
50 mg 6-8 weeks $ 2,180.00
100 mg 6-8 weeks $ 2,800.00
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This compound is a customized synthesis product. We have a strong synthesis team with excellent synthesis technology and capabilities. However, due to various objective factors, there is a low probability that the synthesis will not be successful. If you need to learn more, please feel free to consult us, we will serve you wholeheartedly.
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Biological Description
Chemical Properties
Storage & Solubility Information
Description LY 163443 is an dual receptor antagonist of LTD4 and LTE4.
Synonyms LY163443, LY-163443
Molecular Weight 366.41
Formula C20H22N4O3
CAS No. 97581-70-9

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

TargetMolReferences and Literature

1. Lawrence JW, Kroll DJ, Eacho PI. Ligand-dependent interaction of hepatic fatty acid-binding protein with the nucleus. J Lipid Res. 2000 Sep;41(9):1390-401. PubMed PMID: 10974046. 2. Nuessler V, Pelka-Fleischer R, Zwierzina H, Wilmanns W, Denzlinger C. Effects of progesterone and leukotriene receptor antagonists in experimental models of P-glycoprotein-related resistance. Eur J Med Res. 1997 Apr 21;2(4):159-64. PubMed PMID: 9110922. 3. Eacho PI, Foxworthy PS, Lawrence JW, Herron DK, Noonan DJ. Common structural requirements for peroxisome proliferation by tetrazole and carboxylic acid-containing compounds. Ann N Y Acad Sci. 1996 Dec 27;804:387-402. PubMed PMID: 8993558. 4. Dillard RD, Hahn RA, McCullough D, Carr FP, Rinkema LE, Roman CR, Fleisch JH. (Phenylmethoxy)phenyl derivatives of omega-oxo- and omega-tetrazolylalkanoic acids and related tetrazoles. Synthesis and evaluation as leukotriene D4 receptor antagonists. J Med Chem. 1991 Sep;34(9):2768-78. PubMed PMID: 1654427.

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Keywords

LY 163443 97581-70-9 LY163443 LY-163443 inhibitor inhibit

 

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