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892549-43-8,MFCD18384972
Catalog No.:AA00GT9J

892549-43-8 | MF63

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1mg
≥98%
in stock  
$49.00   $34.00
- +
5mg
≥98%
in stock  
$143.00   $100.00
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10mg
≥98%
in stock  
$262.00   $183.00
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25mg
≥98%
in stock  
$530.00   $371.00
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  • Technical Information
  • Properties
  • Literature
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA00GT9J
Chemical Name:
MF63
CAS Number:
892549-43-8
Molecular Formula:
C23H11ClN4
Molecular Weight:
378.8132
MDL Number:
MFCD18384972
SMILES:
N#Cc1cccc(c1c1[nH]c2c(n1)c1ccccc1c1c2ccc(c1)Cl)C#N
Properties
Computed Properties
 
Complexity:
667  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
28  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
1  
XLogP3:
4.8  

Literature

Title: Dynamic modeling of human 5-lipoxygenase-inhibitor interactions helps to discover novel inhibitors.

Journal: Journal of medicinal chemistry 20120322

Title: Synthesis and SAR study of imidazoquinolines as a novel structural class of microsomal prostaglandin E₂ synthase-1 inhibitors.

Journal: Bioorganic & medicinal chemistry letters 20120101

Title: Trisubstituted ureas as potent and selective mPGES-1 inhibitors.

Journal: Bioorganic & medicinal chemistry letters 20110301

Title: Microsomal prostaglandin e synthase-1 in rheumatic diseases.

Journal: Frontiers in pharmacology 20100101

Title: Discovery of disubstituted phenanthrene imidazoles as potent, selective and orally active mPGES-1 inhibitors.

Journal: Bioorganic & medicinal chemistry letters 20091015

Title: MF498 [N-{[4-(5,9-Diethoxy-6-oxo-6,8-dihydro-7H-pyrrolo[3,4-g]quinolin-7-yl)-3-methylbenzyl]sulfonyl}-2-(2-methoxyphenyl)acetamide], a selective E prostanoid receptor 4 antagonist, relieves joint inflammation and pain in rodent models of rheumatoid and osteoarthritis.

Journal: The Journal of pharmacology and experimental therapeutics 20080501

Title: Substituted phenanthrene imidazoles as potent, selective, and orally active mPGES-1 inhibitors.

Journal: Bioorganic & medicinal chemistry letters 20071215

Title: Xu D et al. MF63 -(6-chloro-1H-phenanthro[9,10-dimidazol-2-yl)-isophthalonitrile, a selective microsomal prostaglandin E synthase-1 inhibitor, relieves pyresis and pain in preclinical models of inflammation. J Pharmacol Exp Ther. 2008 Sep;326(3):754-6

Title: Coté B et al. Substituted phenanthrene imidazoles as potent, selective, and orally active mPGES-1 inhibitors. Bioorg Med Chem Lett. 2007 Dec 15;17(24):6816-20.

Title: Baragatti B, Coceani F.,Dual, constrictor-to-dilator, response of the mouse ductus arteriosus to the microsomal prostaglandin E synthase-1 inhibitor, 2-(6-chloro-1H-phenanthro[9,10dimidazole- 2-yl)isophthalonitrile.,Neonatology. 2011;100(2):139-46. Epub

Title: Giroux A, et al. Discovery of disubstituted phenanthrene imidazoles as potent, selective and orally active mPGES-1 inhibitors.,Bioorg Med Chem Lett. 2009 Oct 15;19(20):5837-41. Epub 2009 Aug 28.

Title: Xu D, L,et al. MF63 -(6-chloro-1H-phenanthro[9,10-dimidazol-2-yl)-isophthalonitrile, a selective microsomal prostaglandin E synthase-1 inhibitor, relieves pyresis and pain in preclinical models of inflammation.,J Pharmacol Exp Ther. 2008 Sep;326(3):75

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