ICAM-1-IN-1

CAS No. 251994-14-6

ICAM-1-IN-1( —— )

Catalog No. M26481 CAS No. 251994-14-6

ICAM-1-IN-1 is a potent and selective E-selectin(IC50 = 7 nM) and ICAM-1(IC50 = 5 nM) inhibitor.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 432 In Stock
5MG 392 In Stock
10MG 587 In Stock
25MG 936 In Stock
50MG 1237 In Stock
100MG 1665 In Stock
200MG Get Quote In Stock
500MG 3339 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    ICAM-1-IN-1
  • Note
    Research use only, not for human use.
  • Brief Description
    ICAM-1-IN-1 is a potent and selective E-selectin(IC50 = 7 nM) and ICAM-1(IC50 = 5 nM) inhibitor.
  • Description
    ICAM-1-IN-1 is a potent and selective E-selectin(IC50 = 7 nM) and ICAM-1(IC50 = 5 nM) inhibitor.(In Vivo):In a rat rheumatoid arthritis model and in a mouse asthma model, ICAM-1-IN-1 shows significant efficacy. The width of inflamed ankles after the ninth day following treatment was reduced by ICAM-1-IN-1, but no efficacy was shown in the acute phase. Treatment with ICAM-1-IN-1 (25 mg/kg) for 21 days significantly reduced eosinophils, serum-soluble ICAM-1 (sICAM-1) and the ankle inflammation of the arthritis rats.
  • In Vitro
    ——
  • In Vivo
    ICAM-1-IN-1 shows significant efficacy in a rat rheumatoid arthritis model and in a mouse asthma model. ICAM-1-IN-1 reduces the width of inflamed ankles after the ninth day following treatment, but shows no efficacy in the acute phase. Treatment with ICAM-1-IN-1 (25 mg/kg) for 21 days significantly reduces the ankle inflammation of the arthritis rats. Significant reduction of eosinophils and serum-soluble ICAM-1 (sICAM-1) is observed.
  • Synonyms
    ——
  • Pathway
    Cell Cycle/DNA Damage
  • Target
    Integrin
  • Recptor
    CDK4| CDK6
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    251994-14-6
  • Formula Weight
    363.23
  • Molecular Formula
    C15H11BrN2O2S
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : ≥ 135 mg/mL (371.67 mM)
  • SMILES
    CNC(=O)c1cc2c(Oc3ccc(Br)cc3)cncc2s1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Zhang P, et al. A phase 1 study of dalpiciclib, a cyclin-dependent kinase 4/6 inhibitor in Chinese patients with advanced breast cancer. Biomark Res. 2021;9(1):24. Published 2021 Apr 12.
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