T25214 |
CCR-11
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CCR 11,CCR11 |
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CCR-11 inhibits bacterial proliferation by suppressing the assembly and GTPase activity of FtsZ. |
TMP-00942 |
Human ACKR2 / CCR D6, His Tag
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TMP-00941 |
Human ACKR2 / CCR D6, Fc Tag
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T14688 |
BMS CCR2 22
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CCR
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BMS CCR2 22 是一种有效的选择性 CC 型趋化因子受体2拮抗剂,钙通量 IC50为 18 nM,趋化性 IC50为1 nM,结合 IC50为5.1 nM。 |
T10708 |
CCR1 antagonist 6
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CCR
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CCR1 antagonist 6是一种 CCR1 拮抗剂(IC50 :3 nM)。 |
T10715 |
CCR6 inhibitor 1
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CCR
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CCR6 inhibitor 1是一种有效的选择性CCR6抑制剂(猴子和人类CCR6的IC50分别为0.45和6 nM)。CCR6在自身免疫性疾病和非自身免疫性疾病中都有关联,因此CCR6 inhibitor 1 作为CCR6的小分子抑制剂... |
T10156 |
CCR3 antagonist 1
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CCR
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CCR3 antagonist 1是一种有效的 CCR3拮抗药,用于炎症和免疫疾病的研究。 |
T10712 |
CCR2 antagonist 3
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AZD2927,AZD-2927 |
CCR
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CCR2 antagonist 3 是 CCR2的拮抗剂。 |
T13114 |
CCR2 antagonist 4
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Teijin compound 1 |
CCR
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CCR2 antagonist 4 是高效的、特异性的CCR2拮抗剂,对 CCR2b 的IC50为 180 nM,抑制 MCP-1 诱导的趋化作用的 IC50为 24 nM。 |
T14900 |
CCR2-RA-[R]
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(5R)-4-乙酰基-1-(4-氯-2-氟苯基)-5-环己基-1,5-二氢-3-羟基-2H-吡咯-2-酮 |
CCR
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CCR2-RA-[R] 是一种 C-C 趋化因子受体 2 型 (CCR2) 变构拮抗剂,IC50值为103 nM。 |
T9983 |
CCR8 antagonist 1
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CCR
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CCR8 antagonist 1 是 C-C Motif 趋化因子受体 8 (CCR8) 的拮抗剂,Ki 值为 1.6 nM。 |
T60145 |
CCR6 antagonist 1
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CCR
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CCR6 antagonist 1 是一种 CCR6 拮抗剂,可抑制 CCL20/CCR6 信号通路。 CCR6 antagonist 1 可用于自身免疫介导的炎症性疾病的研究,如炎症性肠病 (IBDs)。 |
T39661 |
CCR4 antagonist 3
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CCR4 antagonist 3 |
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CCR4 antagonist 3 is an orally active, potent and selective CCR4 antagonist. CCR4 antagonist 3, featuring a novel piperi... |
T10713 |
CCR4 antagonist 2
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Calcium Channel
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CCR4 antagonist 2 (Compound 31) is a novel potent, orally bioavailable small molecule antagonists of CC chemokine recept... |
T10714 |
CCR5 antagonist 1
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CCR
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HIV Protease
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CCR5 antagonist 1 is a CCR5 antagonist extracted from WO 2004054974 A2. It can inhibit HIV replication. |
T10710 |
CCR1 antagonist 9
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CCR
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CCR1 antagonist 9 is an effective and selective CCR1 antagonist (IC50: 6.8 nM in calcium flux assay). |
T10709 |
CCR1 antagonist 7
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CCR
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CCR1 antagonist 7 (compound 16r) 是CCR1的拮抗剂,IC50值为 4 nM。 |
T10711 |
CCR2 antagonist 1
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CCR
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CCR2 antagonist 1 is a high-affinity and long-residence-time antagonist of CCR2 (Ki: 2.4 nM). |
T14899 |
CCR1 antagonist 8
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CCR
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CCR1 antagonist 8, a third azaindazole series compound, is a CCR1 antagonist (IC50: 1.8 nM in Ca2+ flux assay). |
T39662 |
CCR4 antagonist 3 hydrochloride
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CCR4 antagonist 3 hydrochloride is an orally active, potent and selective CCR4 antagonist. CCR4 antagonist 3, featuring ... |