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Piperidine-3-carboxylic acid [5-chloro-4-(5-fluoro-2-methoxy-phenyl)-pyridin-2-yl]-amide

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Piperidine-3-carboxylic acid [5-chloro-4-(5-fluoro-2-methoxy-phenyl)-pyridin-2-yl]-amide Basic information

Product Name:
Piperidine-3-carboxylic acid [5-chloro-4-(5-fluoro-2-methoxy-phenyl)-pyridin-2-yl]-amide
Synonyms:
  • Piperidine-3-carboxylic acid [5-chloro-4-(5-fluoro-2-methoxy-phenyl)-pyridin-2-yl]-amide
  • (3R)-N-[5-Chloro-4-(5-fluoro-2-methoxyphenyl)-2-pyridinyl]-3-piperidinecarboxamide
  • Novartis
  • CDK inhibitor II
  • CDK-IN-2
  • (R)-N-(5-chloro-4-(5-fluoro-2-methoxyphenyl)pyridin-2-yl)piperidine-3-carboxamide
  • CDK inhibitor 2
  • 3-Piperidinecarboxamide, N-[5-chloro-4-(5-fluoro-2-methoxyphenyl)-2-pyridinyl]-, (3R)-
CAS:
1269815-17-9
MF:
C18H19ClFN3O2
MW:
363.81
EINECS:
604-604-1
Mol File:
1269815-17-9.mol
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Piperidine-3-carboxylic acid [5-chloro-4-(5-fluoro-2-methoxy-phenyl)-pyridin-2-yl]-amide Chemical Properties

Boiling point:
525.6±50.0 °C(Predicted)
Density 
1.300
storage temp. 
Store at -20°C
solubility 
Soluble in DMSO
pka
12.16±0.20(Predicted)
form 
Powder
color 
Light yellow to yellow
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Piperidine-3-carboxylic acid [5-chloro-4-(5-fluoro-2-methoxy-phenyl)-pyridin-2-yl]-amide Usage And Synthesis

Uses

CDK-IN-2 is a potent and specific CDK9 inhibitor with IC50 of <8 nM, extracted from reference 1, example 4. IC50 Value: <8 nM [1] Target: CDK9 In vitro: In vivo:

IC 50

CDK9/cyclinT1: 8 nM (IC50)

References

[1] Keith B Pfister, et al. Heteroaryl compounds as kinase inhibitors. 2011, WO2011026917A1.

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Piperidine-3-carboxylic acid [5-chloro-4-(5-fluoro-2-methoxy-phenyl)-pyridin-2-yl]-amide(1269815-17-9)Related Product Information