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1218918-62-7,MFCD22741619
Catalog No.:AA003ALB

1218918-62-7 | Mk-7246

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1mg
≥98%
in stock  
$128.00   $89.00
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5mg
≥98%
in stock  
$565.00   $395.00
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10mg
≥98%
in stock  
$1,000.00   $700.00
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25mg
≥98%
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$1,872.00   $1,310.00
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA003ALB
Chemical Name:
Mk-7246
CAS Number:
1218918-62-7
Molecular Formula:
C21H21FN2O4S
Molecular Weight:
416.4658
MDL Number:
MFCD22741619
SMILES:
OC(=O)Cc1c2CC[C@H](Cn2c2c1cccc2)N(S(=O)(=O)c1ccc(cc1)F)C
Properties
Computed Properties
 
Complexity:
704  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Heavy Atom Count:
29  
Hydrogen Bond Acceptor Count:
6  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
5  
XLogP3:
2.8  

Downstream Synthesis Route

[1]Patent:WO2010/31182,2010,A1.Locationinpatent:Page/Pagecolumn17

[2]JournalofOrganicChemistry,2012,vol.77,p.2299-2309

(+/-){7-(4-fluorophenyl)sulfonyl(methyl)amino-6,7,8,9-tetrahydropyrido1,2-aindol-10-yl}aceticacid 
  1218918-62-7   
C21H21FN2O4S 

[1]BioorganicandMedicinalChemistryLetters,2011,vol.21,p.288-293

[1]BioorganicandMedicinalChemistryLetters,2011,vol.21,p.288-293

[1]JournalofOrganicChemistry,2012,vol.77,p.2299-2309

[1]JournalofOrganicChemistry,2012,vol.77,p.2299-2309

Literature

Title: UGT2B17 genetic polymorphisms dramatically affect the pharmacokinetics of MK-7246 in healthy subjects in a first-in-human study.

Journal: Clinical pharmacology and therapeutics 20120701

Title: CRTH2 antagonist MK-7246: a synthetic evolution from discovery through development.

Journal: The Journal of organic chemistry 20120302

Title: Discovery of potent, selective, and orally bioavailable alkynylphenoxyacetic acid CRTH2 (DP2) receptor antagonists for the treatment of allergic inflammatory diseases.

Journal: Journal of medicinal chemistry 20111027

Title: New indole amide derivatives as potent CRTH2 receptor antagonists.

Journal: Bioorganic & medicinal chemistry letters 20110601

Title: Azaindoles as potent CRTH2 receptor antagonists.

Journal: Bioorganic & medicinal chemistry letters 20110115

Title: Pharmacological characterization of MK-7246, a potent and selective CRTH2 (chemoattractant receptor-homologous molecule expressed on T-helper type 2 cells) antagonist.

Journal: Molecular pharmacology 20110101

Title: Discovery of MK-7246, a selective CRTH2 antagonist for the treatment of respiratory diseases.

Journal: Bioorganic & medicinal chemistry letters 20110101

Title: Gervais FG, et al. Pharmacological characterization of MK-7246, a potent and selective CRTH2 (chemoattractant receptor-homologous molecule expressed on T-helper type 2 cells) antagonist. Mol Pharmacol. 2011 Jan;79(1):69-76.

Title: Gil MA, et al. Anti-inflammatory actions of Chemoattractant Receptor-homologous molecule expressed on Th2 by the antagonist MK-7246 in a novel rat model of Alternaria alternata elicited pulmonary inflammation. Eur J Pharmacol. 2014 Nov 15;743:106-16.

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SDS
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