Ibulocydine

Ibulocydine Suppliers list
Company Name: HANGZHOU CLAP TECHNOLOGY CO.,LTD
Tel: 86-571-88216897,88216896 13588875226
Email: sales@hzclap.com
Products Intro: Product Name:Ibulocydine
CAS:1314096-68-8
Purity:100599% Package:10kg 25kg 200 kilograms per barrel Remarks:good
Company Name: TargetMol Chemicals Inc.
Tel: +17819995354
Email: marketing@targetmol.com
Products Intro: Product Name:Ibulocydine
CAS:1314096-68-8
Package:25mg;1670USD|100mg;2800USD|50mg;2180USD
Company Name: TargetMol Chemicals Inc.  
Tel: 15002134094
Email: marketing@targetmol.cn
Products Intro: Product Name:Ibulocydine
CAS:1314096-68-8
Package:25mg/RMB 11700;100mg/RMB 19500;50mg/RMB 15300
Company Name: Nanjing Shizhou Biology Technology Co.,Ltd  
Tel: 025-85560043 15850508050
Email: cindy.huang@synzest.com
Products Intro: Product Name:Ibulocydine
CAS:1314096-68-8
Purity:98% Package:10mg 100mg

Ibulocydine manufacturers

  • Ibulocydine
  • Ibulocydine pictures
  • $1670.00 / 25mg
  • 2025-08-21
  • CAS:1314096-68-8
  • Min. Order:
  • Purity:
  • Supply Ability: 10g
Ibulocydine Basic information
Product Name:Ibulocydine
Synonyms:Ibulocydine;1H-Pyrrolo[2,3-d]pyrimidine-5-carboxamide, 4-amino-6-bromo-1-[5-O-(2-methyl-1-oxopropyl)-β-L-xylofuranosyl]-
CAS:1314096-68-8
MF:C16H20BrN5O6
MW:458.27
EINECS:
Product Categories:
Mol File:1314096-68-8.mol
Ibulocydine Structure
Ibulocydine Chemical Properties
Boiling point 567.1±60.0 °C(Predicted)
density 1.98±0.1 g/cm3(Predicted)
pka12.82±0.70(Predicted)
Safety Information
MSDS Information
Ibulocydine Usage And Synthesis
DescriptionIbulocydine is a potent CDK inhibitor. Ibulocydine has high activity against Cdk7/cyclin H/Mat1 and Cdk9/cyclin T. Ibulocydine inhibited the growth of HCC cells more effectively than other Cdk inhibitors, including olomoucine and roscovitine, whereas ibulocydine as well as the other Cdk inhibitors and BMK-Y101 minimally influenced the growth of normal hepatocyte cells. Ibulocydine induced apoptosis in HCC cells, most likely by inhibiting Cdk7 and Cdk9. In vitro treatment of HCC cells with ibulocydine rapidly blocked phosphorylation of the carboxyl-terminal domain (CTD) of the large subunit of RNA polymerase II, a process mediated by Cdk7/9. Anti-apoptotic gene products such as Mcl-1, survivin, and X-linked IAP (XIAP) are crucial for the survival of many cell types, including HCC. Following the inhibition of RNA polymerase II phosphorylation, ibulocydine caused rapid down-regulation of Mcl-1, survivin, and XIAP, thus inducing apoptosis. Furthermore, ibulocydine effectively induced apoptosis in HCC xenografts with no toxic side effects. These results suggest that ibulocydine is a strong candidate anti-cancer drug for the treatment of HCC.
Ibulocydine Preparation Products And Raw materials
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