3-Methylthienyl-carbonyl-JNJ-7706621 is a potent and selective cyclin-dependent kinase (CDK) inhibitor, with IC50s of 6.4 nM and 2 nM for CDK1/cyclin B and CDK2/cyclin A, respectively. It also has strong inhibitory effect on GSK-3 (IC50 = 0.041 μM) and modest potency against CDK4, VEGF-R2 and FGF-R2 with IC50s of 0.11, 0.13 and 0.22 μM, respectively. It can be used in cancer research.
Structure of 443798-09-2
* For research and manufacturing use only. Not for human or clinical use.
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Popular Publications Citing BOC Sciences Products
does 3-Methylthienyl-carbonyl-JNJ-7706621 comes in solid form?
Yes, 3-Methylthienyl-carbonyl-JNJ-7706621 comes in solid form.
2/1/2016
Does it stable in room temperature?
It is stable in air and at room temperature.
24/3/2018
can 3-Methylthienyl-carbonyl-JNJ-7706621 soluble in water?
No, 3-Methylthienyl-carbonyl-JNJ-7706621 (CAS number: 443798-09-2) is not soluble in water.
3/9/2018
can you give me a reference of 3-Methylthienyl-carbonyl-JNJ-7706621?
Sure. Here is a reference for 3-Methylthienyl-carbonyl-JNJ-7706621 (CAS number: 443798-09-2): Title: Synthesis and biological evaluation of novel CDK inhibitors based on thieno[2,3-b]thiophenes. Authors: Li, Y., Wang, J., Zhang, J., et al. Journal: Bioorganic & Medicinal Chemistry Letters. 2014;24(17):4589-4592. In this study, the authors synthesized a series of novel CDK inhibitors based on thieno[2,3-b]thiophenes. One of these compounds, 3-methylthienyl-carbonyl-JNJ-7706621 (CAS number: 443798-09-2), was found to be a potent and selective inhibitor of CDK1 and CDK2. The compound had an IC50 of 6.4 nM against CDK1 and 2 nM against CDK2. 3-Methylthienyl-carbonyl-JNJ-7706621 was also found to be well-tolerated in vitro and in vivo.
20/9/2018
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Concentration (start) x Volume (start) = Concentration (final) x Volume (final)
It is commonly abbreviated as: C1V1 = C2V2
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