1049672-75-4 Usage
Uses
Used in Pharmaceutical Industry:
1H-PYRAZOLO[3,4-C]PYRIDIN-5-AMINE is used as a potential anti-cancer agent for its pharmacological activities. It has been studied for its ability to inhibit cancer cell growth and proliferation, making it a promising candidate for the development of new targeted cancer therapies.
1H-PYRAZOLO[3,4-C]PYRIDIN-5-AMINE is also used as a kinase inhibitor, which plays a crucial role in the regulation of various cellular processes. Its potential as a kinase inhibitor could contribute to the development of targeted cancer therapies by specifically inhibiting the activity of enzymes involved in cancer progression.
Used in Research and Development:
1H-PYRAZOLO[3,4-C]PYRIDIN-5-AMINE is used in research for its potential role in the treatment of inflammatory and autoimmune diseases. Its pharmacological properties are being investigated to understand its mechanism of action and to explore its potential as a therapeutic agent for these conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 1049672-75-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,9,6,7 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1049672-75:
(9*1)+(8*0)+(7*4)+(6*9)+(5*6)+(4*7)+(3*2)+(2*7)+(1*5)=174
174 % 10 = 4
So 1049672-75-4 is a valid CAS Registry Number.
1049672-75-4Relevant academic research and scientific papers
Tsikouris, Orestis,Bartl, Tomas,Tousek, Jaromir,Lougiakis, Nikolaos,Tite, Tony,Marakos, Panagiotis,Pouli, Nicole,Mikros, Emmanuel,Marek, Radek
, p. 643 - 649 (2008)
Substituted pyrazolopyridines are potent inhibitors of phosphodiesterases and cyclin-dependent kinases. In this study, NMR was used to investigate the potential NI-H and N2-H tautomerism of 5-substituted pyrazolo[3,4-c]pyridine derivatives. Six compounds were fully characterized by using 1H, 13C, and 15N chemical shifts and indirect 1H-13C and 1H-15N coupling constants. The 1H NMR spectra were measured over a broad range of temperatures. All of the compounds were shown to exist predominantly in the NI-H tautomeric form. Complementary quantum-chemical calculations of the chemical shieldings and indirect spin-spin couplings support the structural conclusions drawn. Copyright
