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Merck
CN

M2692

MK-886 sodium salt hydrate

>98% (HPLC)

Synonym(s):

3-[3-tert-Butylthio-1-(4-chlorobenzyl)-5-isopropyl-1H-indol-2-yl]-2,2-dimethylpropionic acid, sodium salt hydrate

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About This Item

Empirical Formula (Hill Notation):
C27H33NO2ClSNa · xH2O
CAS Number:
Molecular Weight:
494.06 (anhydrous basis)
UNSPSC Code:
12352200
PubChem Substance ID:
MDL number:
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InChI

1S/C27H34ClNO2S.Na.H2O/c1-17(2)19-10-13-22-21(14-19)24(32-26(3,4)5)23(15-27(6,7)25(30)31)29(22)16-18-8-11-20(28)12-9-18;;/h8-14,17H,15-16H2,1-7H3,(H,30,31);;1H2/q;+1;/p-1

SMILES string

O.[Na+].CC(C)c1ccc2n(Cc3ccc(Cl)cc3)c(CC(C)(C)C([O-])=O)c(SC(C)(C)C)c2c1

InChI key

APMAGPLTTCSTMM-UHFFFAOYSA-M

assay

>98% (HPLC)

color

white

solubility

DMSO: 32 mg/mL, H2O: insoluble

storage temp.

2-8°C

Biochem/physiol Actions

Potent and specific inhibitor of leukotriene biosynthesis.

Features and Benefits

This compound was developed by Merck & Co., Inc., Kenilworth, NJ, U.S.. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

Storage Class

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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Chen-Hsuan Wang et al.
Brain research bulletin, 79(3-4), 169-176 (2009-05-12)
Molecules involved in self-protection of neurons against glucose/oxygen/serum deprivation (GOSD) were investigated. Trypan blue dye exclusion assay, Western blotting, ELISA, cytokine antibody array and chemical blocking assay were applied in the study. Results showed that early induction (at 6h of

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