Home Carboxes 136668-42-3
136668-42-3,MFCD00900782
Catalog No.:AA00124G

136668-42-3 | 1H-Indole-2-propanoic acid, 1-[(4-chlorophenyl)methyl]-3-[(1,1-dimethylethyl)thio]-α,α-dimethyl-5-(2-quinolinylmethoxy)-

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1mg
≥98%
in stock  
$96.00   $67.00
- +
5mg
≥98%
in stock  
$428.00   $299.00
- +
10mg
≥98%
in stock  
$712.00   $498.00
- +
25mg
≥98%
in stock  
$1,420.00   $994.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA00124G
Chemical Name:
1H-Indole-2-propanoic acid, 1-[(4-chlorophenyl)methyl]-3-[(1,1-dimethylethyl)thio]-α,α-dimethyl-5-(2-quinolinylmethoxy)-
CAS Number:
136668-42-3
Molecular Formula:
C34H35ClN2O3S
Molecular Weight:
587.1713
MDL Number:
MFCD00900782
SMILES:
Clc1ccc(cc1)Cn1c(CC(C(=O)O)(C)C)c(c2c1ccc(c2)OCc1ccc2c(n1)cccc2)SC(C)(C)C
Properties
Computed Properties
 
Complexity:
873  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
41  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
10  
XLogP3:
8.2  

Literature

Title: Lead modification: amino acid appended indoles as highly effective 5-LOX inhibitors.

Journal: Bioorganic & medicinal chemistry 20140301

Title: MK591, a leukotriene biosynthesis inhibitor, induces apoptosis in prostate cancer cells: synergistic action with LY294002, an inhibitor of phosphatidylinositol 3'-kinase.

Journal: Cancer letters 20100528

Title: 5-Lipoxygenase-activating protein inhibitors. Part 2: 3-{5-((S)-1-Acetyl-2,3-dihydro-1H-indol-2-ylmethoxy)-3-tert-butylsulfanyl-1-[4-(5-methoxy-pyrimidin-2-yl)-benzyl]-1H-indol-2-yl}-2,2-dimethyl-propionic acid (AM679)--a potent FLAP inhibitor.

Journal: Bioorganic & medicinal chemistry letters 20100101

Title: 5-lipoxygenase-activating protein inhibitors: development of 3-[3-tert-butylsulfanyl-1-[4-(6-methoxy-pyridin-3-yl)-benzyl]-5-(pyridin-2-ylmethoxy)-1H-indol-2-yl]-2,2-dimethyl-propionic acid (AM103).

Journal: Journal of medicinal chemistry 20091008

Title: Effect of 5-lipoxygenase inhibitor MK591 on early molecular and signaling events induced by staphylococcal enterotoxin B in human peripheral blood mononuclear cells.

Journal: The FEBS journal 20080601

Title: Substituted 2,2-bisaryl-bicycloheptanes as novel and potent inhibitors of 5-lipoxygenase activating protein.

Journal: Bioorganic & medicinal chemistry letters 20080315

Title: Angiotensin II-induced abdominal aortic aneurysm occurs independently of the 5-lipoxygenase pathway in apolipoprotein E-deficient mice.

Journal: Prostaglandins & other lipid mediators 20070801

Title: Crystal structure of inhibitor-bound human 5-lipoxygenase-activating protein.

Journal: Science (New York, N.Y.) 20070727

Title: Montelukast regulates eosinophil protease activity through a leukotriene-independent mechanism.

Journal: The Journal of allergy and clinical immunology 20060701

Title: Arachidonic acid activates phospholipase D in human neutrophils; essential role of endogenous leukotriene B4 and inhibition by adenosine A2A receptor engagement.

Journal: Journal of leukocyte biology 20030401

Title: Role of 5-lipoxygenase products in the local accumulation of neutrophils in dermal inflammation in the rabbit.

Journal: Journal of immunology (Baltimore, Md. : 1950) 19990915

Title: Assessment of the in vivo biochemical efficacy of orally active leukotriene biosynthesis inhibitors.

Journal: Agents and actions 19930901

Title: Brideau C, et al. Pharmacology of MK-0591 (3--(4-chlorobenzyl)-3-(t-butylthio)-5-(quinolin-2-yl-methoxy)- indol-2-yl-2,2-dimethyl propanoic acid), a potent, orally active leukotriene biosynthesis inhibitor. Can J Physiol Pharmacol. 1992 Jun;70(6):799-807.

Title: Park MS, et al. 5-Lipoxygenase-activating protein (FLAP) inhibitor MK-0591 prevents aberrant alveolarization in newborn mice exposed to 85% oxygen in a dose- and time-dependent manner. Lung. 2011 Feb;189(1):43-50.

Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
SDS
Tags:136668-42-3 Molecular Formula|136668-42-3 MDL|136668-42-3 SMILES|136668-42-3 1H-Indole-2-propanoic acid, 1-[(4-chlorophenyl)methyl]-3-[(1,1-dimethylethyl)thio]-α,α-dimethyl-5-(2-quinolinylmethoxy)-