Catalog |
name |
Description |
price |
R-R-4184 |
BMS CCR2 22 CAS No.445479-97-0 |
BMS CCR2 22/CAS No.445479-97-0 is a potent, specific and high affinity CC-type chemokine receptor 2 (CCR2) antagonist with excellent binding affinity (binding IC50 of 5.1 nM) and potent functional antagonism (calcium flux IC50 of 18 nM and chemotaxis IC50 of 1 nM). |
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R-R-4185 |
CCR2 antagonist 1 CAS No.1683534-96-4 |
CCR2 antagonist 1/CAS No.1683534-96-4 is a high-affinity and long-residence-time CCR2 antagonist, with a Ki of 2.4 nM. |
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R-R-4186 |
SB297006 CAS No.58816-69-6 |
SB297006/CAS No.58816-69-6 is a CCR3 antagonist, which significantly inhibits proliferation and neurosphere formation in CCL11-treated neural progenitor cells. |
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R-R-4187 |
GSK2239633A CAS No.1240516-71-5 |
GSK2239633A/CAS No.1240516-71-5 is a CC-chemokine receptor 4 (CCR4) antagonist, which inhibits the binding of [125I]-TARC to human CCR4 with a pIC50 of 7.96 ± 0.11. |
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R-R-4188 |
LMD-009 CAS No.950195-51-4 |
LMD-009/CAS No.950195-51-4 is a selective CCR8 nonpeptide agonist. LMD-009 mediates chemotaxis, inositol phosphate accumulation, and calcium release in high potencies with EC50s from 11 to 87 nM. |
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R-R-4189 |
RS102895 CAS No.300815-41-2 |
RS102895/CAS No.300815-41-2 is a potent CCR2 antagonist, with an IC50 of 360 nM, and shows no effect on CCR1. |
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R-R-4190 |
CCR2-RA-[R] CAS No.512177-83-2 |
CCR2-RA-[R]/CAS No.512177-83-2 is an allosteric antagonist of the C-C chemokine receptor type 2 (CCR2) with an IC50 of 103 nM. |
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R-R-4191 |
TAK-220 CAS No.333994-00-6 |
TAK-220/CAS No.333994-00-6 is a selective and orally bioavailable CCR5 antagonist, with IC50s of 3.5 nM and 1.4 nM for inhibition on the binding of RANTES and MIP-1α to CCR5, respectively, but shows no effect on the binding to CCR1, CCR2b, CCR3, CCR4, or CCR7; TAK-220 also selectively inhibits HIV-1, with EC50s of 1.2 nM (HIV-1 KK), 0.72 nM (HIV-1 CTV), 1.7 nM (HIV-1 HKW), 1.7 nM (HIV-1 HNK), 0.93 nM (HIV-1 HTN), and 0.55 nM (HIV-1 HHA), and EC90s of 12 nM (HIV-1 KK), 5 nM (HIV-1 CTV), 12 nM (HIV-1 HKW), 28 nM (HIV-1 HNK), 15 nM (HIV-1 HTN), and 4 nM (HIV-1 HHA) in PBMCs. |
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R-R-4192 |
BI 639667 CAS No.1295298-26-8 |
BI 639667 (compound 19n)/CAS No.1295298-26-8, a third azaindazole series compound, is a CCR1 antagonist, with an IC50 of 1.8 nM in Ca2+ flux assay. |
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R-R-4193 |
YM022 CAS No.145084-28-2 |
YM022/CAS No.145084-28-2 is a highly potent, selective and orally active gastrin/cholecystokinin (CCK)-B receptor (CCK-BR) antagonist. YM022 shows the Ki values of 68 pM and 63 nM for CCK-B and CCK-A receptor, respectively. YM022 can inhibit gastrin-induced gastric acid secretion and histidine decarboxylase activation in vivo. |
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