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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:
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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