DRB

CAS No. 53-85-0

DRB( —— )

Catalog No. M21065 CAS No. 53-85-0

DRB is a nucleoside analog that inhibits several carboxyl-terminal domain (CTD) kinases including casein kinase II (IC50 range of 4-10 μM).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
25MG 65 Get Quote
50MG 87 Get Quote
100MG 140 Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    DRB
  • Note
    Research use only, not for human use.
  • Brief Description
    DRB is a nucleoside analog that inhibits several carboxyl-terminal domain (CTD) kinases including casein kinase II (IC50 range of 4-10 μM).
  • Description
    DRB is a nucleoside analog that inhibits several carboxyl-terminal domain (CTD) kinases including casein kinase II (IC50 range of 4-10 μM).
  • In Vitro
    Western Blot Analysis Cell Line:LS174T, HT29, SW48 Concentration:80 μg/mL Incubation Time:24 h Result:Decreased incorporation of [5,6-3H] uridine and increased level of p53 protein.Cell Viability Assay Cell Line:MCF-7, T-47D Concentration:10, 50, 75,100 μM Incubation Time:72 h Result:Inhibited cell-growth in a dose-dependent manner.Resulted in a higher early apoptotic population (5.7 ± 1.1 vs. 2 ± 0.4%) and late apoptotic population (15.9 ± 2.4 vs. 7.7 ± 0.9%) at a concentration of 75 μM.Western Blot Analysis Cell Line:MCF-7 Concentration:75 μM Incubation Time:0.5, 2, 6, 10 h Result:Reduced Mcl-1 protein levels in a time-dependent manner and increased the level of p53 after 6 h.
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Microbiology/Virology
  • Target
    HIV
  • Recptor
    HIV
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    53-85-0
  • Formula Weight
    319.14
  • Molecular Formula
    C12H12Cl2N2O4
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 100 mg/mL (313.34 mM)
  • SMILES
    OC[C@H]1O[C@@H](n2cnc3cc(Cl)c(Cl)cc32)[C@H](O)[C@@H]1O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Marciniak R A Sharp P A . HIV-1 Tat protein promotes formation of more-processive elongation complexes.[J]. Embo Journal 1991 10(13):4189-4196.
molnova catalog
related products
  • Darunavir ethanolate

    A potent, selective HIV-1 protease inhibitor that is extremely potent against laboratory HIV-1 strains and primary clinical isolates with IC50 of 3 nM, IC90 of 9 nM.

  • TAT 48-57

    TAT (48-57) is a cell-permeable peptide, derived from HIV-1 transactivator of transcription (Tat) protein residue 48-57.This peptide is amino acid residues 48 to 57 fragment of the basic domain of HIV Tat.

  • ALW-II-41-27

    ALW-II-41-27, an Eph receptor tyrosine kinase inhibitor, is used for cancer therapy.