SX-682
CAS No. 1648843-04-2
SX-682( —— )
Catalog No. M21976 CAS No. 1648843-04-2
SX-682 is a potent, selective and orally bioavailable inhibitor of CXCR1/2 ,has the potential to treat castration-resistant prostate cancer.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 72 | In Stock |
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| 10MG | 110 | In Stock |
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| 25MG | 205 | In Stock |
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| 50MG | 340 | In Stock |
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| 100MG | 511 | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameSX-682
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NoteResearch use only, not for human use.
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Brief DescriptionSX-682 is a potent, selective and orally bioavailable inhibitor of CXCR1/2 ,has the potential to treat castration-resistant prostate cancer.
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DescriptionSX-682 is a potent, selective and orally bioavailable inhibitor of CXCR1/2 ,has the potential to treat castration-resistant prostate cancer.SX-682 significantly inhibited trafficking of PMN-MDSCs without altering CXCR2 ligand expression. Trafficking of CXCR1+ macrophages was unaltered, possibly due to coexpression of CSF1R. Reduced PMN-MDSC tumor infiltration correlated with enhanced accumulation of endogenous or adoptively transferred T cells. Accordingly, tumor growth inhibition or the rate of established tumor rejection following programed death-axis (PD-axis) immune checkpoint blockade or adoptive cell transfer of engineered T cells was enhanced in combination with SX-682.
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In Vitro——
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In VivoAnimal Model:C57BL/6NTac-Tyrtm1Arte?female mice Dosage:50 mg/kg Administration:Orally; twice a day on a Monday through Friday Result:Has Meager to moderate effects on CRPC progression.
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Synonyms——
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PathwayAutophagy
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TargetCXCR
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RecptorCXCR1|CXCR2
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Research AreaCancer
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IndicationMelanoma Stage IiiMelanoma Stage Iv
Chemical Information
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CAS Number1648843-04-2
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Formula Weight467.2
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Molecular FormulaC19H14BF4N3O4S
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Purity>98% (HPLC)
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SolubilityDMSO:250 mg/mL (535.10 mM; Need ultrasonic)
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SMILESOB(O)c1ccc(OC(F)(F)F)cc1CSc1ncc(cn1)C(=O)Nc1ccc(F)cc1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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TC14012
TC14012, a serum-stable derivative of T140, is a selective and peptidomimetic CXCR4 antagonist with an IC50 of 19.3 nM. TC14012 is a potent CXCR7 agonist with an EC50 of 350 nM for recruiting β-arrestin 2 to CXCR7. TC14012 has anti-HIV activity and anti-cancer activity.
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Ulocuplumab
Ulocuplumab (BMS-936564) is a fully human anti-CXCR4 IgG4 antibody.Ulocplumab exhibits antitumor activity in acute myeloid leukemia (AML), non-Hodgkin's lymphoma (NHL), and multiple myeloma transplantation models.
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AMG 487
AMG 487 prevents the chemokines I-IP-10 and I-ITAC from binding to CXCR3.?In the cellular assays, AMG 487 inhibits CXCR3-mediated cell migration with IC50 values of 8nM, 15nM and 36nM for I-IP-10, I-ITAC and MIG, respectively.
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