CJ-13610

Modify Date: 2024-02-04 13:32:38

CJ-13610 Structure
CJ-13610 structure
Common Name CJ-13610
CAS Number 179420-17-8 Molecular Weight 393.50200
Density N/A Boiling Point N/A
Molecular Formula C22H23N3O2S Melting Point 198 - 200 °C
MSDS Chinese USA Flash Point N/A

 Use of CJ-13610


CJ-13,610, a nonredox-type 5-LO inhibitor, dose dependently suppresses 5-LO product formation in ionophore A23187-stimulated PMNL in the absence of exogenous AA with an IC50 of about 70 nM[1]. PMNL: polymorphonuclear leukocytes; AA: arachidonic acid

 Names

Name 4-[3-[4-(2-methylimidazol-1-yl)phenyl]sulfanylphenyl]oxane-4-carboxamide
Synonym More Synonyms

 CJ-13610 Biological Activity

Description CJ-13,610, a nonredox-type 5-LO inhibitor, dose dependently suppresses 5-LO product formation in ionophore A23187-stimulated PMNL in the absence of exogenous AA with an IC50 of about 70 nM[1]. PMNL: polymorphonuclear leukocytes; AA: arachidonic acid
Related Catalog
References

[1]. Fischer L, et al. Molecular pharmacological profile of the nonredox-type 5-lipoxygenase inhibitor CJ-13,610. Br J Pharmacol. 2004;142(5):861-868.

 Chemical & Physical Properties

Melting Point 198 - 200 °C
Molecular Formula C22H23N3O2S
Molecular Weight 393.50200
Exact Mass 393.15100
PSA 96.43000
LogP 5.01510
Storage condition 2-8°C

 Safety Information

RIDADR NONH for all modes of transport

 Synthetic Route

 Articles1

More Articles
Comparative protection against liver inflammation and fibrosis by a selective cyclooxygenase-2 inhibitor and a nonredox-type 5-lipoxygenase inhibitor.

J. Pharmacol. Exp. Ther. 323(3) , 778-86, (2007)

In this study, we examined the relative contribution of cyclooxygenase-2 (COX-2) and 5-lipoxygenase (5-LO), two major proinflammatory pathways up-regulated in liver disease, to the progression of hepa...

 Synonyms

Tetrahydro-4-[3-[[4-(2-methyl-1H-imidazol-1-yl)phenyl]thio]phenyl]-2H-pyran-4-carboxamide