An improved ensemble learning machine for biological activity prediction of tyrosine kinase inhibitors

2015 ◽  
Vol 29 (4) ◽  
pp. 213-223 ◽  
Author(s):  
Hossein Tavakoli ◽  
Jahan B. Ghasemi
Keyword(s):  
Biological Activity ◽  
Tyrosine Kinase ◽  
Tyrosine Kinase Inhibitors ◽  
Ensemble Learning ◽  
Kinase Inhibitors ◽  
Activity Prediction ◽  
Learning Machine

scholarly journals Synthesis, Reactivity, and Biological Activity of Gold(I) Complexes Modified with Thiourea-Functionalized Tyrosine Kinase Inhibitors

2015 ◽  
Vol 54 (7) ◽  
pp. 3316-3324 ◽  
Author(s):  
Mu Yang ◽  
Amanda J. Pickard ◽  
Xin Qiao ◽  
Matthew J. Gueble ◽  
Cynthia S. Day ◽  
...  
Keyword(s):  
Biological Activity ◽  
Tyrosine Kinase ◽  
Tyrosine Kinase Inhibitors ◽  
Kinase Inhibitors

scholarly journals Expanding the Diversity at the C-4 Position of Pyrido[2,3-d]pyrimidin-7(8H)-ones to Achieve Biological Activity against ZAP-70

2021 ◽  
Vol 14 (12) ◽  
pp. 1311
Author(s):  
Victor Masip ◽  
Ángel Lirio ◽  
Albert Sánchez-López ◽  
Ana B. Cuenca ◽  
Raimon Puig de la Bellacasa ◽  
...  
Keyword(s):  
Biological Activity ◽  
Tyrosine Kinase ◽  
Tyrosine Kinase Inhibitors ◽  
Kinase Inhibitors ◽  
Biologically Active ◽  
Coupling Reactions ◽  
Cross Coupling Reactions ◽  
Dna And Rna ◽  
Wide Range ◽  
Potential Applicability

Pyrido[2,3-d]pyrimidin-7(8H)-ones have attracted widespread interest due to their similarity with nitrogenous bases found in DNA and RNA and their potential applicability as tyrosine kinase inhibitors. Such structures, presenting up to five diversity centers, have allowed the synthesis of a wide range of differently substituted compounds; however, the diversity at the C4 position has mostly been limited to a few substituents. In this paper, a general synthetic methodology for the synthesis of 4-substituted-2-(phenylamino)-5,6-dihydropyrido[2,3-d]pyrimidin-7(8H)-ones is described. By using cross-coupling reactions, such as Ullmann, Buchwald–Hartwig, Suzuki–Miyaura, or Sonogashira reactions, catalyzed by Cu or Pd, we were able to describe new potential biologically active compounds. The resulting pyrido[2,3-d]pyrimidin-7(8H)-ones include N-alkyl, N-aryl, O-aryl, S-aryl, aryl, and arylethynyl substituents at C4, which have never been explored in connection with the biological activity of such heterocycles as tyrosine kinase inhibitors, in particular as ZAP-70 inhibitors.

Side effects of tyrosine kinase inhibitors (TKIs) on bone remodelling

2012 ◽  
Vol 224 (03) ◽  
Author(s):  
JT Tauer ◽  
A Ulmer ◽  
LC Hofbauer ◽  
M Suttorp
Keyword(s):  
Side Effects ◽  
Tyrosine Kinase ◽  
Tyrosine Kinase Inhibitors ◽  
Kinase Inhibitors ◽  
Bone Remodelling
Sign in / Sign up

Export Citation Format

Share Document