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CCR
| Cat. No. | Product Name | CAS No. | Information |
|---|---|---|---|
| CSN12197 | Vicriviroc Maleate | 599179-03-0 | Vicriviroc maleate is a CCR5 antagonist with IC50 of 0.91 nM in clinical development for the treatment of HIV-1. |
| CSN18397 | Vercirnon | 698394-73-9 | Vercirnon is a highly potent antagonist of CCR9, which has been implicated in the aetiology of inflammatory bowel diseases such as Crohns disease. |
| CSN16904 | TAK-220 | 333994-00-6 | TAK-220 is an orally bioavailable small-molecule CCR5 antagonist |
| CSN22613 | SB297006 | 58816-69-6 | SB297006 is a selective antagonist of CCR3 with IC50 of 39 nM |
| CSN18192 | RS-102895 | 300815-41-2 | RS102895 is a potent and specific CCR2 antagonist with binding IC50 of 360 nM, no significant inhibition on CCR1 (IC50 17 M). |
| CSN13797 | RS-102895 HCl | 1173022-16-6 | RS102895 hydrochloride is a potent and specific CCR2 antagonist with binding IC50 of 360 nM, no significant inhibition on CCR1 (IC50 17 M). |
| CSN12845 | RS-504393 | 300816-15-3 | RS 504393 is a selective CCR2 chemokine receptor antagonist (IC50 values are 98 nM and 100 M for inhibition of human recombinant CCR2b and CCR1 receptors respectively). |
| CSN17712 | PF-4136309 | 1341224-83-6 | PF-4136309 is a potent, Selective, and orally bioavailable CCR2 antagonist. |
| CSN17807 | NSC 5844 | 140926-75-6 | NSC 5844 is a bisquinoline compound with C-C chemokine receptor type 1 CCR1-agonistic properties |
| CSN18995 | MK-0812 Succinate | 851916-42-2 | MK-0812 succinate is a potent and selective CCR2 antagonist with low nM affinity for CCR2 on human monocytes |
| CSN13664 | MK-0812 | 624733-88-6 | MK-0812 is a potent and selective CCR2 antagonist with low nM affinity for CCR2 on human monocytes. |
| CSN11361 | Maraviroc | 376348-65-1 | Maraviroc is a selective CCR5 antagonist (IC50 6.4 nM) and displays potent anti-HIV-1 activity. |
| CSN17640 | INCB3344 | 1262238-11-8 | INCB3344 is a potent and selective small molecule antagonist of the mouse CCR2 receptor and inhibits the binding of CCL2 to mouse monocytes with nanomolar potency (IC50 10 nM). |
| CSN13799 | INCB 3284 Dimesylate | 887401-93-6 | INCB 3284 is a potent, selective and orally bioavailable hCCR2 antagonist with IC50 of 3.7 nM. |
| CSN18528 | INCB 3284 | 887401-92-5 | INCB 3284 is a potent, selective and orally bioavailable hCCR2 antagonist with IC50 of 3.7 nM (inhibition of monocyte chemoattractant protein-1 binding to hCCR2). |
| CSN22186 | GW 766994 | 408303-43-5 | GW 766994 is a specific and oral chemokine receptor-3 (CCR3) antagonist, which has entered clinical trial for asthma and eosinophilic bronchitis. |
| CSN22234 | GSK2239633A | 1240516-71-5 | GSK2239633A is a CC-chemokine receptor 4 CCR4 antagonist which inhibits the binding of 125I-TARC to human CCR4 with a pIC50 of 796011 |
| CSN23233 | DAPTA | 106362-34-9 | DAPTA is a potent and selective CCR5 antagonist |
| CSN15987 | Cenicriviroc | 497223-25-3 | Cenicriviroc is an oral, dual CCR2CCR5 antagonist, and displays potent anti-inflammatory and aninfective activity. |
| CSN22175 | CCR5 Antagonist 1 | 716354-86-8 | CCR5 antagonist 1 is a CCR5 antagonist which can inhibit HIV replication extracted from WO 2004054974 A2 |
| CSN18114 | BX471 | 217645-70-0 | BX471 is a potent, selective non-peptide CCR1 antagonist (Ki 1 nM for human CCR1) and exhibits 250-fold selectivity for CCR1 over CCR2, CCR5 and CXCR4. |
| CSN18182 | BX471 HCl | 288262-96-4 | BX471 hydrochloride is a potent, selective non-peptide CCR1 antagonist (Ki 1 nM for human CCR1) and exhibits 250-fold selectivity for CCR1 over CCR2, CCR5 and CXCR4. |
| CSN20665 | AZD-2098 | 566203-88-1 | AZD2098 is a potent CC-chemokine receptor 4 (CCR4) inhibitor, used for asthma research. |
| CSN20666 | AZD-1678 | 942137-41-9 | AZD1678 is a potent CC-chemokine receptor 4 (CCR4) inhibitor, used for asthma research. |
| CSN22732 | C 021 2HCl | 864289-85-0 | |
| CSN22729 | BX 513 HCl | 1216540-18-9 | |
| CSN22720 | BMS CCR2 22 | 445479-97-0 | |
| CSN23102 | SB 328437 | 247580-43-4 | |
| CSN23164 | Teijin Compound 1 | 1313730-14-1 |
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