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497223-28-6,MFCD28502077
Catalog No.:AA01EOIC

497223-28-6 | Cenicriviroc Mesylate

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1mg
99%
1 week  
$193.00   $135.00
- +
5mg
99%
1 week  
$304.00   $213.00
- +
10mg
99%
1 week  
$463.00   $324.00
- +
25mg
99%
1 week  
$876.00   $613.00
- +
50mg
99%
1 week  
$1,447.00   $1,013.00
- +
  • Technical Information
  • Properties
  • Literature
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA01EOIC
Chemical Name:
Cenicriviroc Mesylate
CAS Number:
497223-28-6
Molecular Formula:
C42H56N4O7S2
Molecular Weight:
793.0466
MDL Number:
MFCD28502077
SMILES:
CS(=O)(=O)O.CCCCOCCOc1ccc(cc1)c1ccc2c(c1)C=C(CCCN2CC(C)C)C(=O)Nc1ccc(cc1)[S@@](=O)Cc1cncn1CCC
Properties
Computed Properties
 
Complexity:
1150  
Covalently-Bonded Unit Count:
2  
Defined Bond Stereocenter Count:
1  
Heavy Atom Count:
55  
Hydrogen Bond Acceptor Count:
10  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
17  
Undefined Atom Stereocenter Count:
1  

Literature

Title: A randomized, placebo-controlled trial of cenicriviroc for treatment of nonalcoholic steatohepatitis with fibrosis.

Journal: Hepatology (Baltimore, Md.) 20180501

Title: Isolation and characterization of human immunodeficiency virus type 1 resistant to the small-molecule CCR5 antagonist TAK-652.

Journal: Antimicrobial agents and chemotherapy 20070201

Title: Highly potent and orally active CCR5 antagonists as anti-HIV-1 agents: synthesis and biological activities of 1-benzazocine derivatives containing a sulfoxide moiety.

Journal: Journal of medicinal chemistry 20060323

Title: TAK-652 inhibits CCR5-mediated human immunodeficiency virus type 1 infection in vitro and has favorable pharmacokinetics in humans.

Journal: Antimicrobial agents and chemotherapy 20051101

Title: Lefebvre E, et al. Antifibrotic Effects of the Dual CCR2/CCR5 Antagonist Cenicriviroc in Animal Models of Liver and Kidney Fibrosis. PLoS One. 2016 Jun 27;11(6):e0158156.

Title: Visseaux B, et al. Cenicriviroc, a Novel CCR5 (R5) and CCR2 Antagonist, Shows In Vitro Activity against R5 Tropic HIV-2 Clinical Isolates. PLoS One. 2015 Aug 6;10(8):e0134904.

Title: Lalezari J, et al. Safety, efficacy, and pharmacokinetics of TBR-652, a CCR5/CCR2 antagonist, in HIV-1-infected, treatment-experienced, CCR5 antagonist-naive subjects. J Acquir Immune Defic Syndr. 2011 Jun 1;57(2):118-25.

Title: Baba M, et al. TAK-652 inhibits CCR5-mediated human immunodeficiency virus type 1 infection in vitro and has favorable pharmacokinetics in humans. Antimicrob Agents Chemother. 2005 Nov;49(11):4584-91.

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