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 Related Products (351)
Related Products (351)
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Recombinant Proteins (153)
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Antibodies (9)
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Related Compound Screening Libraries (1)
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CXCR Isoform Comparison
- Polyphemusin II-Derived Peptide
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PMX464
0 ImagesCat. No.: HY-108534CAS No.: 485842-97-5Synonyms: AW 464PMX464 (AW 464) is a thiol-reactive quinol compound and an inhibitor of the thioredoxin-thioredoxin reductase (Trx/TrxR) system, with an IC50 value of 6.5 μM against TrxR. PMX464 acts by irreversibly inhibiting the thioredoxin (Trx-1) system, blocking HIF-1α transcriptional activation and the NF-κB inflammatory pathway, inducing apoptosis, attenuating platelet function and inhibiting thrombosis, and specifically disrupting the trypanothione antioxidant metabolic network in parasites. PMX464 is used in research concerning malignant tumors (colorectal cancer, breast cancer, renal cancer, and leukemia), pulmonary inflammation, African sleeping sickness, and antithrombotic applications. -
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cGAS-IN-9
0 ImagesCat. No.: HY-147129CAS No.: 2369750-66-1cGAS-IN-9 is a cyclic guanosine monophosphate-adenosine monophosphate synthase (cGAS) inhibitor, with IC50 values of 27.5 nM and 5.15 μM against human and murine cGAS, respectively. cGAS-IN-9 shows weak inhibitory activity against human soluble adenylate cyclase, with an IC50 of 26.4 μM. cGAS-IN-9 inhibits dsDNA-induced expression of IFNB1 and CXCL10, as well as activation of the NF-κB pathway, in human immune cells. cGAS-IN-9 can be used in research related to cGAS-dependent inflammatory diseases. -
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BC-1485
0 ImagesCat. No.: HY-114366CAS No.: 2035085-19-7BC-1485 is a small molecule inhibitor of Fibrosis-inducing E3 ligase 1 (FIEL1). BC-1485 protects PIAS4 from ubiquitin-mediated degradation. BC-1485 decreases α-SMA, BAL and CXCL1. BC-1485 ameliorates fibrotic lung injury in murine models. -
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Peptide E5
0 ImagesCat. No.: HY-P11728CAS No.: 1643580-44-2Peptide E5 is an antagonist targeting the CXCR4/CXCL12 axis. Peptide E5 blocks the CXCR4/CXCL12 axis, downregulates CXCR4 expression, and inhibits the phosphorylation of downstream Akt and Erk. Peptide E5 induces apoptosis, suppresses migration and adhesion of breast cancer cells. Peptide E5 inhibits CXCL12-mediated endothelial progenitor cell recruitment, thereby suppressing tumor angiogenesis. Peptide E5 is applicable to relevant research on breast cancer. -
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mDF6002
0 ImagesCat. No.: HY-P992517 -
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- CXCR4-IN-1
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- CTCE-9908 TFA
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Cxcr1 Rat Pre-designed siRNA Set A
0 ImagesCat. No.: HY-RS03399 -
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VB-85247
0 ImagesCat. No.: HY-173404VB-85247 is a STING agonist. VB-85247 induces upregulation of inflammatory cytokines IFNα/β, TNFα, IL6, and CXCL10, as well as maturation and activation of dendritic cells by activating the STING pathway. VB-85247 can achieve regression of intrabladder tumors and can be used in bladder cancer research. -
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CXCR2 antagonist 6
0 ImagesCat. No.: HY-144783CXCR2 antagonist 6 (compound 35c) is a potent CXCR2 antagonist. CXCR2 antagonist 6 shows potent CXCR2 binding affinity (IC50=0.044 µM) and calcium mobilization (IC50=0.66 µM)[ 1]. -
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Cxcr1 Mouse Pre-designed siRNA Set A
0 ImagesCat. No.: HY-RS03398 -
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- TC14012 TFA
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Anti-Mouse CXCR2 Antibody (Cx2Mab-1)
0 ImagesCat. No.: HY-P991746Anti-Mouse CXCR2 Antibody (Cx2Mab-1) reacts with mouse CXCR2 targeting the N-terminal extracellular domain of CXCR2. Recommend Isotype Controls: Rat IgG2b kappa, Isotype Control (HY-P990682). -
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AMD 3465 (Standard)
0 ImagesCat. No.: HY-15971ARCAS No.: 185991-24-6Synonyms: GENZ-644494 (Standard)AMD 3465 (Standard) is the analytical standard of AMD 3465. This product is intended for research and analytical applications. AMD 3465 (GENZ-644494) is a potent antagonist of CXCR4, inhibits binding of 12G5 mAb and CXCL12AF647 to CXCR4, with IC50s of 0.75 nM and 18 nM in SupT1 cells; AMD 3465 also potently inhibits the replication of X4 HIV strains (IC50: 1-10 nM), but has no effect on CCR5-using (R5) viruses. -
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CXCL12 ligand 1
0 ImagesCat. No.: HY-139906CAS No.: 2045891-59-4CXCL12 ligand 1 is the first ligand of the sY12-binding pocket on chemokine CXCL12. -
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CXCR2 antagonist 5
0 ImagesCat. No.: HY-144781CAS No.: 3037517-09-9CXCR2 antagonist 5 (compound 25) is a potent CXCR2 antagonist. CXCR2 antagonist 5 shows potent CXCR2 binding affinity (IC50=0.013 µM) and calcium mobilization (IC50=0.1 µM)[ 1]. -
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Decursin (Standard)
0 ImagesDecursin (Standard) is the analytical standard of Decursin. This product is intended for research and analytical applications. Decursin ((+)-Decursin) is a potent anti-tumor agent. Decursin also is a cytotoxic agent and a potent protein kinase C activator. Decursin induces apoptosis and cell cycle arrest at G1 phase. Decursin decreases the expression of CDK2, CDK4, CDK6, cyclin D1 protein at 48 h. Decursin inhibits cell proliferation and migration. Decursin shows anti-tumor, anti-inflammatory and analgesic activities[4]. -
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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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Your Search Returned No Results.
Sorry. There is currently no product that acts on isoform Bcl-2, Bcl-W and Bim together.Please
try each isoform separately.