CCR
CC chemokine receptor
CCR Isoform Specific Products
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CCR Inhibitors
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CCR Agonists
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CCR Antagonists
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CCR Chemical
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CC Chemokines Proteins
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CCR1 Proteins
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CCR4 Proteins
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CCR5 Proteins
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CCR6 Proteins
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CCR7 Proteins
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CCR8 Proteins
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CCR9 Proteins
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CCR2/CD192 Proteins
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CCR 관련 제품 (302)
관련 제품 (302)
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Recombinant Proteins (164)
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Antibodies (12)
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CCR Isoform Comparison
- CCR5 modulator-1
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Maraviroc-d6
0 ImagesCat. No.: HY-13004SCAS No.: 1033699-22-7Maraviroc-d6 (UK-427857-d6) is the deuterium labeled Maraviroc. Maraviroc (UK-427857) is a selective CCR5 antagonist with activity against human HIV. -
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HFB101110
0 ImagesCat. No.: HY-P992365HFB101110 is a human-derived inhibitor and Treg depleter that specifically targets CCR8. It does not bind to the homologous CCR4 receptor and is mainly used in research on solid tumors, renal cell carcinoma and colorectal cancer. HFB101110 blocks hCCL1 binding by interacting with the N-terminal extracellular domain of hCCR8, thereby inhibiting hCCL1-induced calcium influx, chemotaxis and downstream signaling pathways. Meanwhile, HFB101110 can mediate ADCC effects to specifically deplete CCR8-positive cells, including intratumoral Tregs. HFB101110 exhibits favorable anti-tumor activity and pharmacokinetic properties. -
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Catenarin
0 ImagesCatenarin, an anthraquinone compound, inhibits CCR5- and CXCR4-mediated chemotaxis. Catenarin reduces the phosphorylation of mitogen-activated protein kinases (p38 and JNK) and their upstream kinases (MKK6 and MKK7), and calcium mobilization. Catenarin shows anti-inflammatory effect and suppresses leukocyte migration in the diabetes. Catenarin exhibits significant inhibitory effects against Gram-positive bacteria. Catenarin prevents type 1 diabetes (T1D) in nonobese diabetic mice[1][2]. -
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SLW131
0 ImagesSLW131 is a CCR7 antagonist with a Ki value of 9.85 nM. SLW131 inhibits CCL19-induced Go protein activation with an IC50 of 29.4 μM, and suppresses β-arrestin2 recruitment with an IC50 of 6.0 μM. SLW131 serves as a probe for investigating the biological functions of CCR7 in cells. SLW131 is applicable to research related to rheumatoid arthritis. -
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LUF7996
0 ImagesCat. No.: HY-180571CAS No.: 3104736-80-0LUF7996 is a CCR2 PROTAC Degrader degrading CCR2 with DC50 = 2.6 μM. LUF7996 demonstrates engagement of both and the E3 ligase cereblon and displays sustain and concentration-dependent degradation of CCR2. LUF7996 reliance on the lysosomal pathway to induce CCR2 degradation. LUF7996 efficiently inhibits monocyte migration in virto. -
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cis-J-113863
0 ImagesCat. No.: HY-103360ACAS No.: 202796-41-6Synonyms: UCB35625cis-J-113863 is a competitive chemokine receptor 1 (CCR1) antagonist, with IC50 values of 0.9 and 5.8 nM for human and mouse CCR1 receptors, respectively. -
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PROTAC CCR9 Degrader 1
0 ImagesCat. No.: HY-181287PROTAC CCR9 Degrader 1 is a PROTAC-based degrader targeting CCR9. PROTAC CCR9 Degrader 1 induces ubiquitination, proteasomal degradation of CCR9 and reduces intracellular CCR9 levels by recruiting the VHL E3 ligase. PROTAC CCR9 Degrader 1 has a Ki value of 78.0 nM against human CCR9. PROTAC CCR9 Degrader 1 modulates GPCR activity by binding to the intracellular allosteric binding site of CCR9. PROTAC CCR9 Degrader 1 can be used in research related to Crohn's disease. -
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HZ-1127
0 ImagesCat. No.: HY-P992378HZ-1127 is a thymic stromal lymphopoietin (TSLP) inhibitor. HZ-1127 selectively binds to TSLP, blocks receptor complex interaction, inhibits STAT5 activation, downstream inflammatory signaling, and TSLP-induced CCL17 and CCL22 secretion. HZ-1127 can be used for the research of allergic diseases and cancer. -
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CCR1 antagonist 13
0 ImagesCat. No.: HY-124668ACAS No.: 868408-20-2CCR1 antagonist 13 is a selective CCR1 small molecule antagonist. -
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Histamine glutarimide
0 ImagesCat. No.: HY-165528CAS No.: 1464897-15-1Synonyms: XC8Histamine glutarimide (XC8) is an orally active anti-asthma agent. Histamine glutarimide blocks the maturation of chemokines (CCL2, CCL7, CCL8, CCL13) and inhibits the migration of eosinophils and the degranulation of mast cells. In asthma models induced by carrageenan and rat ovalbumin, Histamine glutarimide can reduce airway resistance and the count of eosinophils in bronchoalveolar lavage fluid. Histamine glutarimide can be used in asthma research. -
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SQA1
0 ImagesCat. No.: HY-162505CAS No.: 1255915-27-5 -
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CCR9 Human Pre-designed siRNA Set A
0 ImagesCat. No.: HY-RS02172 -
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- Ophiobolin C
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Medrysone (Standard)
0 ImagesSynonyms: HMS (Standard); 6α-Methyl-11β-hydroxyprogesterone (Standard)Medrysone (Standard) is the analytical standard of Medrysone. This product is intended for research and analytical applications. Medrysone (HMS; 6α-Methyl-11β-hydroxyprogesterone) is a STAT6 modulator and M2 macrophage polarization inducer. Medrysone enhances IL-4-triggered STAT6 activation, upregulates the expression of M2 markers, and promotes the secretion of VEGF and CCL2. Medrysone also enhances the pro-migratory activity of M2-like macrophages toward endothelial cells. By regulating macrophage polarization and related repair pathways, Medrysone significantly promotes corneal wound repair in a rat mechanical injury model. Medrysone can be used for research related to corneal injury. -
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CCR6 antagonist 4
0 ImagesCat. No.: HY-176980CCR6 antagonist 4 (compound OXM1) is a potent and selective CC chemokine receptor 6 (CCR6) allosteric antagonist (IC50 = 158 nM). CCR6 antagonist 4 binds to an extracellular pocket and disrupts the receptor activation network. CCR6 antagonist 4 can be used for chronic inflammatory diseases research. -
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Reftinirsen inapertide
0 ImagesCat. No.: HY-185930CAS No.: 3119104-59-2Reftinirsen inapertide is a CNOT3 inhibitor. CNOT3 is a non-catalytic subunit of the CCR4-NOT complex, serving as a direct transcriptional repressor and penetrance modifier of PRPF31. Reftinirsen inapertide can be used for the research of retinal dystrophies associated with prpf31 mutations. -
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Vercirnon (Standard)
0 ImagesSynonyms: GSK-1605786 (Standard); CCX282-B (Standard); Traficet-EN (Standard)Vercirnon (Standard) is the analytical standard of Vercirnon. This product is intended for research and analytical applications. Vercirnon (GSK1605786A) is an orally bioavailable, selective, and potent antagonist of CCR9. Vercirnon inhibits CCR9-mediated Ca2+ mobilization and chemotaxis on Molt-4 cells with IC50 values of 5.4 and 3.4 nM, respectively. Vercirnon is selective for CCR9 over CCR1-12 and CX3CR1-7 (IC50s>10 μM for all). Vercirnon is an equipotent inhibitor of CCL25-directed chemotaxis of both splice forms of CCR9 (CCR9A and CCR9B) with IC50 values of 2.8 and 2.6 nM, respectively. -
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CCR2 antagonist 6
0 ImagesCat. No.: HY-185299CAS No.: 1421063-89-9CCR2 antagonist 6 (Example 98) is a CCR2 antagonist (Kb: 0.215 μM for CCR2, 0.174 μM for hCCR2B). CCR2 antagonist 6 can be used in the research of inflammation and autoimmune diseases. -
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GSK2239633A (Standard)
0 ImagesCat. No.: HY-100183RCAS No.: 1240516-71-5GSK2239633A (Standard) is the analytical standard of GSK2239633A (HY-100183). This product is intended for research and analytical applications. GSK2239633A is a CC-chemokine receptor 4 (CCR4) antagonist, which inhibits the binding of [125I]-TARC to human CCR4 with a pIC50 of 7.96. -
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Sorry. There is currently no product that acts on isoform Bcl-2, Bcl-W and Bim together.Please
try each isoform separately.