lavendustin B

CAS No. 125697-91-8

lavendustin B( Lavendustin B )

Catalog No. M17227 CAS No. 125697-91-8

Lavendustin B is a Tyrosine Kinase Inhibitor and an inhibitor of HIV-1 integrase (IN) interaction with its cognate cellular cofactor, lens epithelium-derived growth factor (LEDGF/p75).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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2MG 71 In Stock
5MG 110 In Stock
10MG 178 In Stock
25MG 403 In Stock
50MG 592 In Stock
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Biological Information

  • Product Name
    lavendustin B
  • Note
    Research use only, not for human use.
  • Brief Description
    Lavendustin B is a Tyrosine Kinase Inhibitor and an inhibitor of HIV-1 integrase (IN) interaction with its cognate cellular cofactor, lens epithelium-derived growth factor (LEDGF/p75).
  • Description
    Lavendustin B is a Tyrosine Kinase Inhibitor amd an inhibitor of HIV-1 integrase (IN) interaction with its cognate cellular cofactor, lens epithelium-derived growth factor (LEDGF/p75).
  • In Vitro
    In HL-60 cells, Lavendustin B (0-1000 μM) inhibits the uptake of methylglucose, deoxyglucose, and dehydroascorbic acid in human erythrocytes in a dose-dependent manner, with 50% inhibition observed at approximately 10-30 μM. Moreover, increasing concentrations of Lavendustin B inhibited, in a dose-dependent manner, the binding of cytochalasin B to human erythrocyte membranes.
  • In Vivo
    ——
  • Synonyms
    Lavendustin B
  • Pathway
    Neuroscience
  • Target
    GluR
  • Recptor
    Tyrosine Kinase inhibitor| HIV-1 integrase
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    125697-91-8
  • Formula Weight
    365.39
  • Molecular Formula
    C21H19NO5
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 50 mg/mL (136.84 mM)
  • SMILES
    O=C(O)c1cc(N(Cc2ccccc2O)Cc2ccccc2O)ccc1O
  • Chemical Name
    5-[Bis[(2-hydroxyphenyl)methyl]amino]-2-hydroxy-benzoic Acid

Shipping & Storage Information

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

Reference

1.Agharbaoui FE, et al. Computational and synthetic approaches for developing Lavendustin B derivatives as allosteric inhibitors of HIV-1 integrase. Eur J Med Chem. 2016 Nov 10;123:673-83
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