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SCH-900875

SCH-900875 is an orally active, brain-penetrant and selective CXCR3 receptor inhibitor, which also shows high selectivity over CXCR1 and CXCR2 receptors. SCH-900875 binds to CXCR3, blocking the binding of ligands CXCL9, CXCL10, and CXCL11, inhibiting downstream G protein and β-arrestin signaling pathways to suppress inflammatory cell migration. SCH-900875 is promising for research of autoimmune diseases (rheumatoid arthritis, multiple sclerosis) and inflammatory disorders (psoriasis, inflammatory bowel disease) [1][2].

Product Specifications

CAS Number

[907206-98-8]

UNSPSC

12352005

Target

Arrestin; CXCR

Related Pathways

GPCR/G Protein; Immunology/Inflammation

Field of Research

Inflammation/Immunology

Purity

98.16

Solubility

DMSO : 100 mg/mL (ultrasonic)

Smiles

O=C(C1=CC=C(Cl)C=C1)N2CCC(N3[C@@H](CC)CN(C4=NC=C(C5=NN=C(NCC)O5)N=C4C)[C@H](C)C3)CC2

Molecular Formula

C28H37ClN8O2

Molecular Weight

553.10

References & Citations

[1]Frank Xing Chen, et al. Process and intermediates for the Synthesis of heterocyclic Substituted Piperazines with CXCR3 Antagonist Activity. US20110124867A1. 2011-05-26.|[2]Andrews SP, Cox RJ. Small Molecule CXCR3 Antagonists. J Med Chem. 2016 Apr 14;59 (7) :2894-917.

Shipping Conditions

Room Temperature

Storage Conditions

-20°C, 3 years; 4°C, 2 years (Powder)

Scientific Category

Reference compound1

Clinical Information

No Development Reported

Isoform

CXCR1; CXCR2; CXCR3

Available Sizes

Curated Selection

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