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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CCR4 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 (302)
Related Products (302)
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Recombinant Proteins (164)
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Antibodies (12)
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CCR Isoform Comparison
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Ccr7 Mouse Pre-designed siRNA Set A
0 ImagesCat. No.: HY-RS02167 -
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JNJ-17166864
0 ImagesCat. No.: HY-129991CAS No.: 874887-03-3JNJ-17166864 is a highly selective CCR2 antagonist. JNJ-17166864 has low oral bioavailability. JNJ-17166864 can significantly reduce the area of alveolar bone loss in a mouse model of periodontitis induced by Porphyromonas gingivalis infection. JNJ-17166864 can be used in the research of inflammatory diseases such as allergic rhinitis and periodontitis. -
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INCB9471
0 ImagesCat. No.: HY-14230CAS No.: 869769-98-2INCB9471 is a potent, selective and orally active CCR5 antagonist. INCB9471 shows anti-HIV-1 activity. -
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- Fuscin
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YM-344484
0 ImagesCat. No.: HY-182736CAS No.: 671205-14-4YM-344484 is an orally active dual antagonist of chemokine CCR3 receptor and histamine histamine H1 receptor. YM-344484 inhibits ligand-induced Ca2+ influx, chemotaxis of CCR3-expressing cells, histamine-induced Ca2+ influx, increased vascular permeability and eosinophil accumulation. YM-344484 suppresses vascular permeability and inhibits eosinophil infiltration in a mouse asthma model. YM-344484 can be used in research related to asthma, allergic rhinitis and atopic dermatitis. -
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- SD-24
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Vicriviroc
0 ImagesCat. No.: HY-B0155CAS No.: 306296-47-9Synonyms: SCH 417690; SCH-D; MK-7690 free baseVicriviroc (SCH 417690) is an orally active CCR5 antagonist with the IC50 of 10 nM, and also inhibts MIP-1α and intracellular calcium release induced by the ligand RANTES (10 nM) with the IC50 values of 0.91 nM and 16 nM,,respectively. Vicriviroc can inhibits human immunodeficiency virus type 1 (HIV-1) infection, and can also used for study of cancer. -
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- LUF8100
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Anti-CCL28 Antibody
0 ImagesCat. No.: HY-P992198 -
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Ccr2 Mouse Pre-designed siRNA Set A
0 ImagesCat. No.: HY-RS02152 -
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- CXCR2/CCR7 antagonist-1
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Viscumneoside V
0 ImagesViscumneoside V is a plant-derived anti-inflammatory agent present in Viscum album var. coloratum. Viscumneoside V inhibits the expression of MCP-1 and promotes the production of RANTES in LPS-stimulated immune cells. Viscumneoside V can be used for research related to skin rashes. -
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Velaprumig
0 ImagesCat. No.: HY-P991168CAS No.: 2988741-17-7Velaprumig is a monoclonal antibody targeting human CD99, CCL25, and anti-human Aβ (Aβ-47F). Velaprumig regulates immune cell migration and reduces β-amyloid-related pathological processes, exerting immunomodulatory and potential anti - Alzheimer's disease activities. -
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Ccr2 Rat Pre-designed siRNA Set A
0 ImagesCat. No.: HY-RS02153 -
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CP-481715
0 ImagesCat. No.: HY-12079CAS No.: 212790-31-3CP-481715 is a potent, reversible and selective CCR1 antagonist with a Kd of 9.2 nM for human CCR1. CP-481715 is >100-fold selective for CCR1 as compared with a panel of G-protein-coupled receptors including related chemokine receptors. CP-481715 has the potential for rheumatoid arthritis and other inflammatory diseases research. -
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GSK-2239633
0 ImagesCat. No.: HY-122565CAS No.: 2181665-31-4GSK-2239633 is an indazole arylsulfonamide-based CCR4 antagonist. GSK-2239633 is applicable to research related to asthma. -
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CCR4 Human Pre-designed siRNA Set A
0 ImagesCat. No.: HY-RS02157 -
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Enzelkitug (FUT8-KO)
0 ImagesCat. No.: HY-P991135ASynonyms: RO-7502175 (FUT8-KO); RG-6411 (FUT8-KO)Enzelkitug (RO-7502175; RG-6411) (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. Enzelkitug (FUT8-KO) can be used for the research of various solid tumors and hematological malignancies. -
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ALK4290 dihydrochloride
0 ImagesCat. No.: HY-136788ACAS No.: 1372127-19-9Synonyms: AKST4290 dihydrochloride; BI144807 dihydrochlorideALK4290 dihydrochloride (AKST4290 dihydrochlorid) is a potent and orally active CCR3 inhibitor extracted from patent US20130261153A1, compound Example 2, with a Ki of 3.2 nM for hCCR3. ALK4290 can be used for the research of neovascular age-related macular degeneration and Parkinsonism. -
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PF-232798
0 ImagesCat. No.: HY-14388CAS No.: 849753-15-7 -
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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.