CCR
CC chemokine receptor
CCR Isoform Specific Products
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CCR Inhibitors
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CC Chemokines Proteins
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CCR1 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 Related Products (303)
Related Products (303)
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Recombinant Proteins (164)
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Antibodies (12)
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CCR Isoform Comparison
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CH0076989
0 ImagesCat. No.: HY-136881CAS No.: 954371-52-9CH0076989 is a specific CCR3 agonist. CH0076989 activates eosinophils and transfectants expressing both wild-type CCR3 and a CCR1:CCR3 chimaeric receptor lacking the CCR3 amino-terminus. CH0076989 has a direct interaction with the transmembrane helices of CCR3, supported by the complete loss of its activity due to mutations of the residues Y41, Y113 and E287. CH0076989 can be used for the study of inflammation and allergic diseases (such as asthma). -
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CXCR2 antagonist 10
0 ImagesCat. No.: HY-181681CXCR2 antagonist 10 (Compound 10b) is a CCR2 antagonist with an IC50 of 0.48 μM. CXCR2 antagonist 10 also exhibits antagonistic activity against CXCR2/CCR7, with IC50 values of 4.18 μM and 2.07 μM, respectively. CXCR2 antagonist 10 is applicable for cancer research. -
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Anti-CCL2 (Carlumab)-MC-Vc-PAB-SN38
0 ImagesCat. No.: HY-171684Anti-CCL2 (Carlumab)-MC-Vc-PAB-SN38 is an antibody-drug conjugate (ADC) consisting of the humanized anti-CCL2 (chemokine ligand 2) antibody Carlumab (HY-P99188) conjugated to the linker Mc-VC-PAB and the topoisomerase I inhibitor SN38 (HY-13704). The ADC toxic molecule and linker part are Mc-VC-PAB-SN38 (HY-131057). Anti-CCL2 (Carlumab)-MC-Vc-PAB-SN38 can be used in cancer research. -
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PLS-123
0 ImagesCat. No.: HY-120406CAS No.: 1431727-04-6LPS-123 is a covalently irreversible BTK inhibitor with an IC50 of < 5 nM. LPS-123 simultaneously inhibits the catalytic activity of BTK at Tyr551 and its self-activation at Tyr223. LPS-123 inhibits phosphorylation of the AKT/mTOR and MAPK signaling pathways, activation of PLCγ2, ERK1/2, p38, AKT, and mTOR, and blocks the production of CCL3 and CCL4 chemokines. LPS-123 exhibits significant anti-proliferative activity against various B-cell lymphoma cell lines and effectively induces apoptosis via a caspase-dependent pathway. LPS-123 also demonstrates significant antitumor activity in the OCI-Ly7 xenograft model. LPS-123 can be used for lymphoma research. -
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Zn-DPA-maytansinoid conjugate 1
0 ImagesCat. No.: HY-151559CAS No.: 3034629-04-1Zn-DPA-maytansinoid conjugate 1 is a small molecule-based maytansinoid conjugate targeting immune checkpoint. Zn-DPA-maytansinoid conjugate 1 induces lasting regression of tumor growth and rejuvenates tumor microenvironment (TME) to an "inflamed hot tumor" . -
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ST45177901
0 ImagesCat. No.: HY-182564CAS No.: 618865-88-6ST45177901 is a CC chemokine receptor 4 (CCR4) antagonist. The combination of ST45177901 and Sorafenib (HY-10201) effectively inhibits the chemotaxis of Treg cells via the CCL22/CCL17-CCR4 signaling pathway, thereby significantly suppressing the growth and metastasis of tumor cells. ST45177901 is applicable to liver cancer research. -
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Anti-CCR9 Antibody
0 ImagesCat. No.: HY-P992199 -
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CCL17-IN-2
0 ImagesCat. No.: HY-185145CAS No.: 3104330-35-7CCL17-IN-2 (Compound Ex.128) is a CCL17 secretion inhibitor with an EC50 of 0.3 nM. CCL17-IN-1 can be used in the research of autoimmune diseases, dermatological conditions, and respiratory disorders. -
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Ccr1 Mouse Pre-designed siRNA Set A
0 ImagesCat. No.: HY-RS02148 -
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RO5234444
0 ImagesCat. No.: HY-100819CAS No.: 1365266-79-0RO5234444 is an orally active CCR2 antagonist, with IC50s of 22nM for human CCR2 and 161 nM for mouse CCR2. RO5234444 alleviates glomerulosclerosis, reduces albuminuria, and significantly improves the glomerular filtration rate (GFR) in the uninephrectomized (1K) type 2 diabetic db/db mouse model. RO5234444 can be used for the study of type 2 diabetic nephropathy. -
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TAK-661
0 ImagesCat. No.: HY-159927CAS No.: 175215-34-6TAK-661 is a inhibitor of eosinophil chemotaxis. TAK-661 significantly reduces the bronchoconstriction during the late phase, along with the inhibition of eosinophilia in bronchoalveolar lavage (BAL) and the eosinophil infiltration into the airway wall. -
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Ccr9 Mouse Pre-designed siRNA Set A
0 ImagesCat. No.: HY-RS02173 -
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VCH-286
0 ImagesCat. No.: HY-15571ACAS No.: 891824-47-8VCH-286 is a CCR5 inhibitor that exhibits potent in vitro anti-HIV-1 activity when used alone. -
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CMPD167
0 ImagesCat. No.: HY-124848CAS No.: 313994-79-5Synonyms: MRK-1 -
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ZL-1218 (FUT8-KO)
0 ImagesCat. No.: HY-P991944AZL-1218 (FUT8-KO) is an anti-CCR8 monoclonal antibody expressed by CHO cells with the fucosyltransferase 8 gene (FUT8) knocked out. Fucose deficiency enhances the antibody-dependent cellular cytotoxicity (ADCC) effect of the antibody. ZL-1218 (FUT8-KO) can be used for the research of solid tumour. -
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YM-344031
0 ImagesCat. No.: HY-160998CAS No.: 671204-98-1YM-344031 is an orally active antagonist for CCR3. YM-344031 inhibits binding of Eotaxin-1 and RANTES to CCR3, with IC50 of 3.0 and 16.3 nM. YM-344031 inhibits ligand-induced rise in intracellular Ca[2+] and the ligand-induced chemotaxis. YM-344031 inhibits eotaxin-1-induced changes in eosinophil morphology in macaques blood, and prevents allergic skin reactions in a mouse allergy model. -
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Anti-CCR5 Antibody (HEK/1/85a/7a)
0 ImagesCat. No.: HY-P991843Anti-CCR5 Antibody (HEK/1/85a/7a) recognizes an epitope on human CCR5. CCR5 is a seven-transmembrane G-protein-coupled receptor (GPCR). Recommend Isotype Controls: Rat IgG2b kappa, Isotype Control (HY-P990682). -
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Anti-CCR1 Antibody
0 ImagesCat. No.: HY-P991938 -
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CCR1 antagonist 12
0 ImagesCat. No.: HY-124668CAS No.: 921208-19-7CCR1 antagonist 12 (Compound 12) is an antagonist for CCR1 with IC50 of 3 nM for human CCR1. CCR1 antagonist 12 inhibits CCL3-induced transwell chemotaxis with an IC50 of 0.009 µM. CCR1 antagonist 12 exhibits good pharmacokinetic characters in rats model. -
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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.