From €89.00 €75.65
Cenicriviroc is an orally bioavailable antagonist of C-C chemokine receptor type 5 (CCR5) and CCR2 that inhibits binding of macrophage inflammatory protein 1? (MIP-1?; IC50 = 2.3 nM) and monocyte chemotactic protein 1 (MCP-1; IC50 = 5.9 nM), respectively, in CHO cells.{41586} Cenicriviroc is also an antagonist of CCR3 and CCR4 (IC50s = 2.4 and 1.1 ?M, respectively), however, it does not inhibit agonist binding to CCR1 or CCR7 at concentrations up to 10 ?M. At a concentration of 100 nM, cenicriviroc completely inhibits replication of R5 HIV-1 in U87.CD4.CCR5 cells. Cenicriviroc inhibits replication of the R5 HIV-1 strains JR-FL and KK in peripheral blood mononuclear cells (PBMCs) with EC50 values ranging from 21 to 210 pM and 33 to 91 pM, respectively. In vivo, cenicriviroc (20 mg/kg per day) reduces collagen deposition, levels of collagen type 1 protein and mRNA expression, and non-alcoholic fatty liver disease activity score in a mouse model of non-alcoholic steatohepatitis (NASH).{41587} It also reduces collagen type 1 protein levels, mRNA expression, and collagen deposition in a mouse model of unilateral ureter obstruction and a rat model of thioacetamide-induced liver fibrosis.
Territorial Availability: Available through Bertin Technologies only in France
| Size | 1 mg, 10 mg, 5 mg, 500 µg |
|---|---|
| Shipping | dry ice |
| CAS number | 497223-25-3 |
| Molecular formula | C41H52N4O4S |
| Smiles | CCCCOCCOC1=CC=C(C2=CC=C(N(CC(C)C)CCC/C(C(NC3=CC=C([S@](CC4=CN=CN4CCC)=O)C=C3)=O)=C5)C5=C2)C=C1, CCCCOCCOC1=CC=C(C2=CC=C(N(CC(C)C)CCC/C(C(NC3=CC=C([S@](CC4=CN=CN4CCC)=O)C=C3)=O)=C5)C5=C2)C=C1, CCCCOCCOC1=CC=C(C2=CC=C(N(CC(C)C)CCC/C(C(NC3=CC=C([S@](CC4=CN=CN4CCC)=O)C=C3)=O)=C5)C5=C2)C=C1, CCCCOCCOC1=CC=C(C2=CC=C(N(CC(C)C)CCC/C(C(NC3=CC=C([S@](CC4=CN=CN4CCC)=O)C=C3)=O)=C5)C5=C2)C=C1 |
| Molecular weight | 696,9 |
| Custom code | 2933.29 |
| Formulation | A crystalline solid |
| Purity | ≥95% |
| UNSPSC code | 12352100 |
Cayman Chemical’s mission is to help make research possible by supplying scientists worldwide with the basic research tools necessary for advancing human and animal health. Our utmost commitment to healthcare researchers is to offer the highest quality products with an affordable pricing policy.
Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.
Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.
Our organic and analytical chemists specialize in the rapid development of manufacturing processes and analytical methods to carry out clinical and commercial GMP-API production. Pre-clinical drug discovery efforts are currently underway in the areas of bone restoration and repair, muscular dystrophy, oncology, and inflammation. A separate group of Ph.D.-level scientists are dedicated to offering Hit-to-Lead Discovery and Profiling Services for epigenetic targets. Our knowledgeable chemists can be contracted to perform complete sample analysis for analytes measured by the majority of our assays. We also offer a wide range of analytical services using LC-MS/MS, HPLC, GC, and many other techniques.
Accreditations
ISO/IEC 17025:2005
ISO Guide 34:2009
Cayman is a leader in the field of emerging drugs of abuse, providing high-purity Schedule I-V Controlled Substances to federally-licensed laboratories and qualified academic research institutions for forensic analyses. We are certified by ACLASS Accreditation Services with dual accreditation to ISO/IEC 17025:2005 and ISO Guide 34:2009.
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