Cat. No. Name Size Price Add Cart
KI2030SCH 5637055 mg$686.4
SCH 56370510 mg$943.8
SCH 56370550 mg$2745.6
SCH 563705200 mg$6292

Chemical Characteristic

Product NameSCH 563705
SynonymsN/A
CAS No.473728-58-4
Molecular Weight 425.48
FormulaC23H27N3O5
Chemical Name3-((3-((dimethylamino)carbonyl)-2-hydroxyphenyl)amino)-4-(((r)-1-(4-isopropylfuran-2-yl)propyl)amino)cyclobut-3-ene-1,2-dione
SmilesC1(=O)C(=O)C(=C1NC(CC)c1occ(c1)C(C)C)Nc1c(c(ccc1)C(=O)N(C)C)O
Chemical Structure

Biological activities

SCH 563705 is a potent CXCR2 and CXCR1 antagonist with Ki values of 1 and 3 nM, respectively. SCH 563705 inhibits chemokine binding to human CXCR2 and CXCR1 with IC50s of 1.3 and 7.3 nM, respectively. SCH 563705 also inhibits both Gro-alpha and IL-8 induced human polymorphonuclear leukocytes (hPMN) migration in vitro.[1] SCH 563705 selectively reduces the peripheral blood neutrophil frequency, and increases the CXCR2 ligand CXCL1.[2] In addition, SCH 563705 has good oral pharmacokinetic profiles in rat, mouse, monkey, and dog.[1]

Protocols

In vivo: SCH 563705 is dissolved in the vehicle 0.4% hydroxypropyl methyl cellulose (MC).[2]

References

[1] Chao J, et al. C(4)-alkyl substituted furanyl cyclobutenediones as potent, orally bioavailable CXCR2 and CXCR1 receptor antagonists. Bioorg Med Chem Lett. 2007, 17(13): 3778-3783.
[2] Min SH, et al. Pharmacological targeting reveals distinct roles for CXCR2/CXCR1 and CCR2 in a mouse model of arthritis. Biochem Biophys Res Commun. 2010, 391(1): 1080-1086.

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