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
• Empirical Formula (Hill Notation): C₂₇H₃₃NO₂ClSNa · xH₂O
• CAS Number: 118427-55-7
• Molecular Weight: 494.06 (anhydrous basis)
• MDL number: MFCD11045945
• UNSPSC Code: 12352200
• PubChem Substance ID: 24278612

Properties

• Assay: >98% (HPLC)
• color: white
• solubility: DMSO: 32 mg/mL; H₂O: insoluble
• storage temp.: 2-8°C
• SMILES string: O.[Na+].CC(C)c1ccc2n(Cc3ccc(Cl)cc3)c(CC(C)(C)C([O-])=O)c(SC(C)(C)C)c2c1
• 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
• InChI key: APMAGPLTTCSTMM-UHFFFAOYSA-M

Description

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.

Safety Information

• Storage Class Code: 13 - Non Combustible Solids
• WGK: WGK 3
• Flash Point(F): Not applicable
• Flash Point(C): Not applicable
• Personal Protective Equipment: dust mask type N95 (US), Eyeshields, Gloves