CXCR
CXC chemokine receptors; C-X-C motif chemokine receptors
CXCR Isoform Specific Products
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CXCR Inhibitors
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CXCR Agonists
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CXCR Antagonists
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CXCR Activators
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CXCR Modulators
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CXCR Inducer
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CXCR Degrader
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CXCR Controls
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CXCR Ligand
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CXC Chemokines Proteins
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CXC Chemokine Receptor Proteins
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CXCR2 Proteins
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CXCR3 Proteins
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CXCR4 Proteins
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CXCR Produits associés (354)
Produits associés (354)
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Protéines Recombinantes (153)
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Anticorps (9)
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Related Compound Screening Libraries (1)
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CXCR Isoform Comparison
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KY1051
0 ImagesCat. No.: HY-P992397KY1051 is a human monoclonal antibody targeting CXCR4/CD184. KY1051 can be used for research related to tumor immunology. -
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CXCR4 modulator-1
0 ImagesCat. No.: HY-146053CAS No.: 2987682-11-9CXCR4 modulator-1 (compound ZINC72372983) is a potent CXCR4 modulator with an EC50 value of 100 nM. CXCR4 modulator-1 can be used for researching anti-inflammatory, anticancer and anti-HIV. -
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SDF-1α (human)
0 ImagesCat. No.: HY-P4911CAS No.: 1268129-65-2SDF-1α (human) is a mononuclear cells chemoattractant that can bind to CXCR4. SDF-1α plays a central role in stem cell homing, retention, survival, proliferation, cardiomyocyte repair, angiogenesis and ventricular remodelling following myocardial infarction. SDF-1α (human) can be used in cardiovascular disease research. -
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(R)-SCH 546738
0 Images(R)-SCH 546738 is the R-isomer of SCH 546738 (HY-10017). SCH 546738 is an orally active and non-competitive antagonist for CXCR3 with Ki of 0.4 nM for human CXCR3 receptor. -
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CXCR4 antagonist 3
0 ImagesCat. No.: HY-144286CAS No.: 2761009-43-0CXCR4 antagonist 3 (compound 12a) is a potent antagonist of CXCR4 with an IC50 of 11 nM. CXCR4 antagonist 3 is a congener of TIQ15. CXCR4 antagonist 3 demonstrates the best overall properties including CXCR4 antagonism, CYP 2D6 inhibition, metabolic stability, and permeability. CXCR4 antagonist 3 has the potential for the research of human immunodeficiency virus. -
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Cyclazosin
0 ImagesCat. No.: HY-184086CAS No.: 139953-73-4Cyclazosin is an α1D-adrenergic receptor antagonist and a partial agonist of CXCR4/ACKR3. The pKi values of Cyclazosin for cloned human α1D, α1B and α1A adrenergic receptors are 9.28, 9.23 and 8.18, respectively. Cyclazosin induces β-arrestin recruitment in CXCR4 and ACKR3 with EC50 values of 16 μM and 10 μM, respectively, stimulates ERK1/2 phosphorylation, and induces receptor internalization. Cyclazosin potently inhibits CXCL12-induced chemotaxis of primary human aortic vascular smooth muscle cells. Cyclazosin alters MDMA-induced thermoregulatory responses in mice, converting monophasic hyperthermia to a biphasic pattern without affecting resting core body temperature. Cyclazosin can be used for diseases related to tumor metastasis, MDMA-induced hyperthermia and vasoconstriction. -
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UCUF-965
0 ImagesCat. No.: HY-182850CAS No.: 2965316-77-0UCUF-965 is a CXCR4 positive allosteric modulator. UCUF-965 potentiates CXCL12-induced β-arrestin recruitment and cAMP signaling, activates lymphoblast migration, induces calcium flux, and does not bind CXCR4’s orthosteric CXCL12 site. UCUF-965 reduces miR-15b and miR-29a levels, increases miR-146a levels in fibroblasts. UCUF-965 enhances angiogenesis and reduces wound healing time in diabetic mice. UCUF-965 can be used for the research of diabetic wound healing impairment. -
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CXCR4-IN-2
0 ImagesCat. No.: HY-149558CXCR4-IN-2 (compound A1) is a bifunctional fluorinated small molecule that is a potent CXCR4 inhibitor with anticancer activity. CXCR4-IN-2 has cytotoxic (IC50: 60 μg/mL; 72 h) and antiproliferative effects on mouse colorectal cancer (CRC) cells. CXCR4-IN-2 induces cell arrest in the G2/M phase and induces apoptosis. -
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SMU-3k
0 ImagesCat. No.: HY-183607SMU-3k is a STING activator and PD-L1 inhibitor, with a PD-L1 IC50 of 106 nM, a KD of 386 nM for human PD-L1, and a KD of 352 nM for murine PD-L1. SMU-3k activates the STING pathway, induces phosphorylation of TBK1 and IRF3, and promotes the expression of IFN-β, IL-6 and CXCL10. SMU-3k blocks the PD-1/PD-L1 interaction, reduces PD-L1 levels and induces PD-L1 internalization. Through dual immunomodulation, SMU-3k exerts synergistic tumor growth inhibitory effects in a mouse colon cancer model. SMU-3k can be used for the research of colon cancer. -
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- HL82624
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Sirt1/CXCR3-IN-1
0 ImagesCat. No.: HY-184899Sirt1/CXCR3-IN-1 is a dual Sirt1/CXCR3 inhibitor with an IC50 of 0.77 μM against Sirt1. Sirt1/CXCR3-IN-1 inhibits dengue virus replication, upregulates the expression of interferon-stimulated genes, and enhances the antiviral defense capacity of the host. Sirt1/CXCR3-IN-1 suppresses CXCR3-mediated T cell chemotaxis and cytokine release, thereby reducing immune activation and inflammatory responses. Sirt1/CXCR3-IN-1 is applicable to research related to dengue virus infection. -
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SFB-AMD3465
0 ImagesCat. No.: HY-158317CAS No.: 2416231-90-6 -
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- E70K
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CXCR1 Human Pre-designed siRNA Set A
0 ImagesCat. No.: HY-RS03397 -
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STING-IN-18
0 ImagesCat. No.: HY-181057STING-IN-18 is an orally active STING inhibitor. STING-IN-18 exhibits an IC50 of 86 nM against STING in murine RAW-LuciaTM ISG cells. STING-IN-18 inhibits STING activation and blocks downstream signaling pathways. STING-IN-18 suppresses kidney injury and inflammation. STING-IN-18 can be used for the research of autoimmune and inflammatory diseases. -
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CXCR4 antagonist 4
0 ImagesCat. No.: HY-144285CAS No.: 2761009-30-5CXCR4 antagonist 4 is a potent, orally active CXCR4 antagonist (IC50=24 nM) with diminished CYP 2D6 activity, improved PAMPA permeability, potent inhibition of human immunodeficiency virus entry (IC50=7 nM). -
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CXCR4-antagonist-11
0 ImagesCat. No.: HY-182909CAS No.: 2892568-27-1CXCR4-antagonist-11 is a CXCR4 antagonist with CXCR4 IC50 values of 68.9 nM and 48.3 nM. CXCR4-antagonist-11 modulates CXCR4 receptor function. CXCR4-antagonist-11 demonstrates high permeability, selectivity against CYP 2D6, and a high hERG index. CXCR4-antagonist-11 shows improved oral exposure in mouse pharmacokinetic studies. -
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VUF11207 TFA
0 ImagesCat. No.: HY-115615CAS No.: 1492153-74-8 -
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- TBS6b
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- NoxaBH3
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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.