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Catalog | name | Description | price |
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R-R-4261 | AMD 3465 hexahydrobromide CAS No.185991-07-5 | AMD 3465 hexahydrobromide (GENZ-644494 hexahydrobromide)/CAS No.185991-07-5 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. | price> |
R-C-2562 | HO-3867 CAS:1172133-28-6 | HO-3867 is a selective and potent STAT3 inhibitor.HO-3867 selectively inhibited STAT3 phosphorylation,transcription,and DNA binding without affecting the expression of other active STATs.HO-3867 exhibited minimal toxicity toward noncancerous cells and tissues but induced apoptosis in ovarian cancer cells. | price> |
R-R-4262 | CXCR7 modulator 2 CAS No.2227426-37-9 | CXCR7 modulator 2/CAS No.2227426-37-9 is a modulator of C-X-C Chemokine Receptor Type 7 (CXCR7), with a Ki of 13 nM. | price> |
R-C-2563 | STATTIC CAS:19983-44-9 | Stattic is a potent STAT3 inhibitor and inhibits STAT3 phosphorylation(at Y705 and S727).Stattic inhibits the binding of a high affinity phosphopeptide for the SH2 domain of STAT3.Stattic ameliorates the renal dysfunction in Alport syndrome (AS)mice. | price> |
R-R-4263 | CXCR2 antagonist 8 CAS No.182498-30-2 | CXCR2 antagonist 8/CAS No.182498-30-2 is a potent and selective CXCR2 antagonist. CXCR2 antagonist 8 can be used for insulin resistance research. | price> |
R-C-2564 | Belumosudil (KD025, SLx-2119) CAS:911417-87-3 | Belumosudil(KD025)is a selective inhibitor of ROCK2 with IC50s of 105nM and 24 µM for ROCK2 and ROCK1,respectively.Anti-fibrotic properties. | price> |
R-R-4264 | CXCR7 antagonist-1 hydrochloride CAS No.2990472-61-0 | CXCR7 antagonist-1 hydrochloride/CAS No.2990472-61-0 is a CXCR7 antagonist that inhibits the binding of the SDF-1 chemokine (also known as the CXCL12 chemokine) or I-TAC (also known as CXCL11) to the chemokine receptor CXCR7. CXCR7 antagonist-1 hydrochloride is useful in preventing tumor cell proliferation, tumor formation, inflammatory diseases, and many other diseases (extracted from patent WO2014085490A1, compound 1.128). | price> |
R-C-2565 | MDK83190 CAS:79183-19-0 | MDK83190 is a potent apoptosis activator,induces Apaf-1 oligomerization, increases procaspase-9 processing and subsequent caspase-3 activation in a cyto c-dependent Manner. | price> |
R-R-4265 | Ladarixin sodium CAS No.865625-56-5 | Ladarixin sodium (DF 2156A)/CAS No.865625-56-5 is an orally active, allosteric non-competitive and dual CXCR1 and CXCR2 antagonist. Ladarixin sodium can be used for the research of COPD and asthma. | price> |
R-C-2566 | IDF-11774 CAS:1429054-28-3 | IDF-11774 is a hypoxia-inducible factor-1(HIF-1)inhibitor.It reduces the HRE-luciferase activity of HIF-1α(IC50=3.65μM)and blocks HIF-1α accumulation under hypoxia in HCT116 human colon cancer cells. | price> |
R-R-4266 | ATI-2341 TFA | ATI-2341 is a potent and functionally selective allosteric agonist of C-X-C chemokine receptor type 4 (CXCR4), which functions as a biased ligand, favoring Gαi activation over Gα13. ATI-2341 activates the inhibitory heterotrimeric G protein (Gi) to promote inhibition of cAMP production and induce calcium mobilization. ATI-2341 is a potent and efficacious mobilizer of bone marrow polymorphonuclear neutrophils (PMNs) and hematopoietic stem and progenitor cells (HSPCs). | price> |
R-R-4267 | USL311 CAS No.1373268-67-7 | USL311/CAS No.1373268-67-7 is a potent and selective CXCR4 antagonist, with anti-tumor activity. USL311 prevents the binding of stromal-cell derived factor-1 (SDF-1 or CXCL12) to CXCR4. | price> |
R-R-4268 | CXCR2-IN-2 CAS No.1838123-21-9 | CXCR2-IN-2/CAS No.1838123-21-9 is a selective, brain penetrant, and orally bioavailable CXCR2 antagonist (IC50=5.2 nM/1 nM in β-arrestin assay/CXCR2 Tango assay, respectively). CXCR2-IN-2 displays ~730-fold selectivity over CXCR1 and >1900-fold selectivity over all other chemokine receptors. CXCR2-IN-2 inhibits human whole blood Gro-α induced CD11b expression with an IC50 of 0.04 μM. | price> |
R-R-4269 | Ulocuplumab CAS No.1375830-34-4 | Ulocuplumab (Anti-Human CXCR4 Recombinant Antibody/BMS-936564/MDX1338)/CAS No.1375830-34-4 is a fully human IgG4 anti-CXCR4 antibody. Ulocuplumab induces apoptosis and inhibits CXCL12 mediated CXCR4 activation-migration of chronic lymphocytic leukemia (CLL). Ulocuplumab exhibits antitumor activity in established tumors including acute myeloid leukemia (AML), non-Hodgkin lymphoma (NHL), and multiple myeloma xenograft models. | price> |
R-C-2570 | Zotarolimus CAS:221877-54-9 | Zotarolimus(ABT-578)is a derivative of rapamycin(HY-10219),with anti-proliferative activity.Zotarolimus is an immunosuppressant.Zotarolimus is developed specifically for local delivery from stents for the prevention of coronary artery restenosis. | price> |
R-R-4270 | SRT3190 CAS No.1204707-73-2 | SRT3190/CAS No.1204707-73-2 is an antagonist of CXCR2, used in the research of chemokine mediated diseases. | price> |
R-C-2571 | Carmoisine CAS:154-93-8 | Carmustine(bis-chloroethylnitrosourea,BCNU,BiCNU)is a cell-cycle phase nonspecific alkylating antineoplastic agent and used in the treatment of brain tumors and various other malignant neoplasms. | price> |
R-R-4271 | ALX 40-4C Trifluoroacetate | ALX 40-4C Trifluoroacetate is a small peptide inhibitor of the chemokine receptor CXCR4, inhibits SDF-1 from binding CXCR4 with a Ki of 1 μM, and suppresses the replication of X4 strains of HIV-1; ALX 40-4C Trifluoroacetate also acts as an antagonist of the APJ receptor, with an IC50 of 2.9 μM. | price> |
R-C-2572 | Metolazone CAS:17560-51-9 | Metolazone(SR-720-22)is primarily used to treat congestive heart failure and high blood pressure. | price> |
R-R-4272 | CTCE-9908 CAS No.1030384-98-5 | CTCE-9908/CAS No.1030384-98-5 is a potent and selective CXCR4 antagonist. CTCE-9908 induces mitotic catastrophe, cytotoxicity and inhibits migration in CXCR4-expressing ovarian cancer cells. | price> |