SCH-527123

CAS No. 473727-83-2

SCH-527123( SCH527123 | Navarixin | SCH 527123 | MK-7123 )

Catalog No. M14572 CAS No. 473727-83-2

A potent, selective, orally bioavailable CXCR2/CXCR1 receptor antagonist with Kd of 0.08 and 41 nM for cynomolgus CXCR2 and CXCR1, respectively.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 80 In Stock
10MG 120 In Stock
25MG 219 In Stock
50MG 357 In Stock
100MG 537 In Stock
500MG 1188 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    SCH-527123
  • Note
    Research use only, not for human use.
  • Brief Description
    A potent, selective, orally bioavailable CXCR2/CXCR1 receptor antagonist with Kd of 0.08 and 41 nM for cynomolgus CXCR2 and CXCR1, respectively.
  • Description
    A potent, selective, orally bioavailable CXCR2/CXCR1 receptor antagonist with Kd of 0.08 and 41 nM for cynomolgus CXCR2 and CXCR1, respectively; potently inhibits CXCR2-mediated chemotaxis with IC50 of 3-6 nM; inhibits neutrophil recruitment, mucus production, and goblet cell hyperplasia in animal models of pulmonary inflammation.COPD Phase 2 Discontinued.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    SCH527123 | Navarixin | SCH 527123 | MK-7123
  • Pathway
    GPCR/G Protein
  • Target
    Chemokine Receptor
  • Recptor
    Chemokine Receptor
  • Research Area
    Inflammation/Immunology
  • Indication
    COPD

Chemical Information

  • CAS Number
    473727-83-2
  • Formula Weight
    397.4244
  • Molecular Formula
    C21H23N3O5
  • Purity
    >98% (HPLC)
  • Solubility
    10 mM in DMSO
  • SMILES
    O=C(N(C)C)C1=CC=CC(NC2=C(N[C@@H](C3=CC=C(C)O3)CC)C(C2=O)=O)=C1O
  • Chemical Name
    Benzamide, 2-hydroxy-N,N-dimethyl-3-[[2-[[(1R)-1-(5-methyl-2-furanyl)propyl]amino]-3,4-dioxo-1-cyclobuten-1-yl]amino]-

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Chapman RW, et al. J Pharmacol Exp Ther. 2007 Aug;322(2):486-93. 2. Dwyer MP, et al. J Med Chem. 2006 Dec 28;49(26):7603-6. 3. Gonsiorek W, et al. J Pharmacol Exp Ther. 2007 Aug;322(2):477-85. 4. Singh S, et al. Clin Cancer Res. 2009 Apr 1;15(7):2380-6.
molnova catalog
related products
  • BMS-681

    A potent and orally bioavailable dual antagonist of CCR2 and CCR5 with binding IC50 of 0.7 nM and 2.4 nM, respectively.

  • IT1t

    A highly potent, selective, orally bioavailable CXCR4 inhibitor with binding IC50 of 8 nM for hCXCR4, IC50 of 1.1 nM in Ca2+-mobilization assays.

  • ML 604086

    ML 604086 (ML604086) is a potent, selective CCR8 inhibitor that inhibits CCL1 mediated chemotaxis and increases in intracellular Ca2+ concentrations with IC50 of 1.3?uM and 1.0?uM respectively in cellular assays.