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Catalog | name | Description | price |
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R-R-4152 | Bindarit CAS No.130641-38-2 | Bindarit (AF2838)/CAS No.130641-38-2 is a selective inhibitor of the monocyte chemotactic proteins MCP-1/CCL2, MCP-3/CCL7, and MCP-2/CCL8, and no effect on other CC and CXC chemokines such as MIP-1α/CCL3, MIP-1β/CCL4, MIP-3/CCL23. Bindarit also has anti-inflammatory activity. | price> |
R-C-2453 | BNC210 CAS:13589-06-5 | BNC210(H-Ile-Trp-OH;IW-2143)is a α7 nAChR negative allosteric modulator. BNC210 has potent activity in animal models of anxiety and depression. | price> |
R-R-4153 | INCB3344 CAS No.1262238-11-8 | INCB3344/CAS No.1262238-11-8 is a potent, selective and orally bioavailable CCR2 antagonist with IC50 values of 5.1 nM (hCCR2) and 9.5 nM (mCCR2) in binding antagonism and 3.8 nM (hCCR2) and 7.8 nM (mCCR2) in antagonism of chemotaxis activity. | price> |
R-C-2454 | VU0238441 CAS:85511-68-8 | VU0238441 is a pan muscarinic acetylcholine receptor(mAChR)positive allosteric modulator(PAM)with EC50s of 3.2 μM,2.8μM,2.2μM,2.1μM,>10μM for M1,M2,M3,M5 and M4,respectively. | price> |
R-R-4154 | Ilacirnon CAS No.1100318-47-5 | CCX140 (CCX140-B)/CAS No.1100318-47-5 is a potent CCR2 antagonist. | price> |
R-C-2455 | VU0119498 CAS:79183-37-2 | VU0119498 is a pan Gq mAChR M1,M3,M5 positive allosteric modulator(PAM), with EC50s of 6.04,6.38,and 4.08µM,respectively.VU0119498 has antidiabetic activity. | price> |
R-R-4155 | (1S)-CCR2 antagonist 1 CAS No.1683534-97-5 | (1S)-CCR2 antagonist 1/CAS No.1683534-97-5 is a left-handed chiral body of CCR2 antagonist 1 (HY-112792). CCR2 antagonist 1 is a high-affinity and long-residence-time CCR2 antagonist, with a Ki of 2.4 nM. | price> |
R-C-2456 | benzylquinolone carboxylic acid CAS:338747-41-4 | BQCA(benzylquinolone carboxylic acid)is a highly selective positive allosteric modulator of the M1 muscarinic acetylcholine receptor(mAChR). | price> |
R-R-4156 | RS102895 hydrochloride CAS No.1173022-16-6 | RS102895 hydrochloride/CAS No.1173022-16-6 is a potent CCR2 antagonist, with an IC50 of 360 nM, and shows no effect on CCR1. | price> |
R-C-2457 | VU0238429 CAS:1160247-92-6 | VU 0238429 is positive allosteric modulator of muscarinic acetylcholine receptor subtype 5(mAChR5 or M5),with an EC50 of 1.16μM. | price> |
R-R-4157 | Cenicriviroc CAS No.497223-25-3 | Cenicriviroc (TAK-652)/CAS No.497223-25-3 is an orally active, dual CCR2/CCR5 antagonist, also inhibits both HIV-1 and HIV-2, and displays potent anti-inflammatory and antiinfective activity. | price> |
R-C-2458 | JHU37152 CAS:2369979-67-7 | JHU37152 is a potent and brain-penetrant DREADD agonist,with EC50s of 5 nM and 0.5 nM for hM3Dq and hM4Di DREADDs in HEK-293 cells,respectively. JHU37152 exhibits selective [3H]Clozapine displacement from DREADDs and not from other Clozapine-binding sites in mice brain tissue. | price> |
R-R-4158 | TAK-779 CAS No.229005-80-5 | TAK-779/CAS No.229005-80-5 is a potent and selective nonpeptide antagonist of CCR5 and CXCR3, with a Ki of 1.1 nM for CCR5, and effectively and selectively inhibits R5 HIV-1, with EC50 and EC90 of 1.2 nM and 5.7 nM, respectively, in MAGI-CCR5 cells. | price> |
R-C-2459 | JHU37160 CAS:2369979-68-8 | JHU37160 is a potent and brain-penetrant DREADD agonist,with EC50s of 18.5 nM and 0.2 nM for hM3Dq and hM4Di DREADDs in HEK-293 cells,respectively.JHU37160 exhibits selective Clozapine displacement from DREADDs and not from other Clozapine-binding sites in mice brain tissue. | price> |
R-R-4159 | Zelnecirnon CAS No.2366152-15-8 | Zelnecirnon (RPT193)/CAS No.2366152-15-8 is an orally active inhibitor of CCR4, blocks the recruitment of Th2 inflammatory immune cells into inflamed tissues. Zelnecirnon can be used for allergic inflammation in atopic dermatitis, asthma, and other diseases research. | price> |
R-C-2460 | Varenicline Tartrate (CP 526555-18) CAS:375815-87-5 | Varenicline Tartrate(CP 526555;Champix)is a nicotinic receptor partial agonist; it stimulates nicotine receptors more weakly than nicotine itself does. | price> |
R-R-4160 | CCR6 antagonist 1 CAS No.588674-64-0 | CCR6 antagonist 1/CAS No.588674-64-0 is a CCR6 antagonist that inhibits the CCL20/CCR6 axis. CCR6 antagonist 1 can be used in the research of autoimmune-mediated inflammatory diseases, such as inflammatory bowel diseases (IBDs). | price> |
R-C-2461 | Bethanechol chloride CAS:590-63-6 | Bethanechol chloride(Carbamyl-β-methylcholine chloride),a parasympathomimetic agent,is a mAChR agonist that exerts its effects via directly stimulating the mAChR(M1,M2,M3,M4,and M5)of the parasympathetic nervous system. | price> |
R-R-4161 | CCR6 inhibitor 1 CAS No.2437547-04-9 | CCR6 inhibitor 1/CAS No.2437547-04-9 is a potent and selective CCR6 inhibitor, with IC50s of 0.45 and 6 nM for monkey and human CCR6, much more selective at CCR6 over human CCR1 (IC50, > 30000 nM), and CCR7 (IC50, 9400 nM). CCR6 inhibitor 1 markedly blocks ERK phosphorylation. CCR6 inhibitor 1 is used in the research of autoimmune diseases and cancer. | price> |
R-C-2462 | Pilocarpine HCl CAS:54-71-7 | Pilocarpine Hydrochloride is a potent M3-type muscarinic acetylcholine receptor(M3 muscarinic receptor)agonist. | price> |