SX-517
- Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
- Dry Ice Shipment: No


SX-517
Description :
SX-517 is a dual CXCR2/1 antagonist, containing boronic acid. SX-517 inhibits CXCL1-induced Ca2+ flux (IC50=38 nM), and antagonizes CXCL8-induced [ (35) S]GTPγS binding (IC50=60 nM) and ERK1/2 phosphorylation. SX-517 has significant ability for inflammation suppression, in both humanized polymorphonuclear (PMN) cells and in murine model[1][2].UNSPSC :
12352005Target :
CXCRType :
Reference compoundRelated Pathways :
GPCR/G Protein; Immunology/InflammationApplications :
COVID-19-immunoregulationField of Research :
Inflammation/ImmunologyAssay Protocol :
https://www.medchemexpress.com/sx-517.htmlConcentration :
10mMPurity :
99.90Solubility :
DMSO : 100 mg/mL (ultrasonic)Smiles :
OB(C1=CC=CC=C1CSC2=NC=C(C(NC3=CC=C(F)C=C3)=O)C=C2)OMolecular Formula :
C19H16BFN2O3SMolecular Weight :
382.22References & Citations :
[1]2-[5- (4-Fluorophenylcarbamoyl) pyridin-2-ylsulfanylmethyl]phenylboronic Acid (SX-517) : Noncompetitive Boronic Acid Antagonist of CXCR1 and CXCR2. J Med Chem. 2014 Oct 23;57 (20) :8378-97. |[2]Ti H, et al. Targeted Treatments for Chronic Obstructive Pulmonary Disease (COPD) Using Low-Molecular-Weight Drugs (LMWDs) . J Med Chem. 2019 Jul 11;62 (13) :5944-5978.Shipping Conditions :
Room TemperatureStorage Conditions :
4°C (Powder, sealed storage, away from moisture and light)Scientific Category :
Reference compound1Clinical Information :
No Development ReportedIsoform :
CXCR1; CXCR2CAS Number :
[1240494-13-6]

