Ibulocydine

CAS No. 1314096-68-8

Ibulocydine( Ibulocydine )

Catalog No. M11259 CAS No. 1314096-68-8

Ibulocydine is the prodrug of CDK inhibitor BMK-Y101, inhibits CDK7 and CDK9 with IC50 of 530 nM and 85 nM in kinase assays, respectively.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 963 Get Quote
50MG 1962 Get Quote
100MG 2520 Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    Ibulocydine
  • Note
    Research use only, not for human use.
  • Brief Description
    Ibulocydine is the prodrug of CDK inhibitor BMK-Y101, inhibits CDK7 and CDK9 with IC50 of 530 nM and 85 nM in kinase assays, respectively.
  • Description
    Ibulocydine is the prodrug of CDK inhibitor BMK-Y101, inhibits CDK7 and CDK9 with IC50 of 530 nM and 85 nM in kinase assays, respectively; reduces the phosphorylation of RNA polymerase II at Ser-5 and Ser-2, down-regulates Mcl-1, survivin, and XIAP and induces apoptosis; shows effectivity in HCC xenografts with no toxic side effects.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    Ibulocydine
  • Pathway
    Angiogenesis
  • Target
    CDK
  • Recptor
    CDK
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1314096-68-8
  • Formula Weight
    458.269
  • Molecular Formula
    C16H20BrN5O6
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    CC(C)C(OC[C@@H]1O[C@H](N2C=NC(N)=C3C2=NC(Br)=C3C(N)=O)[C@@H](O)[C@@H]1O)=O
  • Chemical Name
    ((2S,3S,4S,5S)-5-(4-amino-6-bromo-5-carbamoyl-1H-pyrrolo[2,3-d]pyrimidin-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl isobutyrate

Shipping & Storage Information

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

Reference

1. Cho SJ, et al. J Biol Chem. 2011 Jun 3;286(22):19662-71. 2. Park SS, et al. Radiother Oncol. 2014 Aug;112(2):295-301. 3. Park SS,, et al. Int J Biochem Cell Biol. 2017 Feb;83:47-55.
molnova catalog
related products
  • SU-9516

    A selective CDK2 inhibitor with IC50 of 22 nM; shows less potent for CDK1/CDK4(IC50=40/200 nM), no inhibition on PKC, EGFR, p38MAPK; decreases the phosphorylation of pRb, and increases caspase-3 activation.

  • CDK9-IN-1

    CDK9-IN-1 is a potent, selective CDK9 inhibitor with IC50 of 39 nM (CDK9/CycT1), >10-fold selectivity over CDK4 and >100-fold over CDK1/2/3/5/6/7, inhibits HIV-1 replication in cellular assays.

  • KB-0742 dihydrochlor...

    KB-0742 dihydrochloride is a potent, selective and orally inhibitor of ?CDK9.