109547-60-6Relevant articles and documents
Discovery of mixed type thymidine phosphorylase inhibitors endowed with antiangiogenic properties: Synthesis, pharmacological evaluation and molecular docking study of 2-thioxo-pyrazolo[1,5-a][1,3,5]triazin-4-ones. Part II
Bera, Hriday,Ojha, Probir Kumar,Tan, Bee Jen,Sun, Lingyi,Dolzhenko, Anton V.,Chui, Wai-Keung,Chiu, Gigi Ngar Chee
, p. 294 - 303 (2014/04/17)
In our drug discovery program, a series of 2-thioxo-pyrazolo[1,5-a][1,3,5] triazin-4-ones were designed, synthesized and evaluated for their TP inhibitory potential. All the synthesized analogues conferred a varying degree of TP inhibitory activity, comparable or better than positive control, 7-deazaxanthine (7-DX, 2) (IC50 value = 42.63 μM). A systematic approach to the lead optimization identified compounds 3c and 4a as the most promising TP inhibitors, exhibiting mixed mode of enzyme inhibition. Moreover, selected compounds demonstrated the ability to attenuate the expression of the angiogenic markers (viz. MMP-9 and VEGF) in MDA-MB-231 cells at sublethal concentrations. In addition, molecular docking studies revealed the plausible binding orientation of these inhibitors towards TP, which was in accordance with the experimental results. Taken as a whole, these compounds would constitute a new direction for the design of novel TP inhibitors with promising antiangiogenic properties.
PROLYL HYDROXYLASE INHIBITORS
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Page/Page column 17, (2009/04/25)
The invention described herein relates to certain bicyclic heteroaromatic N-substituted glycine derivatives of formula (I) which are antagonists of HIF prolyl hydroxylases and are useful for treating diseases benefiting from the inhibition of this enzyme, anemia being one example.
Synthesis of 4-Alkylpyrazoles from 3,5-Diaminopyrazoles
Echevarria, Aurea,Elguero, Jose,Yranzo, Gloria I.,Diez-Bara, Enrique,Hoz, Antonio de la,et al.
, p. 2229 - 2232 (2007/10/02)
The possibility of preparing 4-alkylpyrazole from malononitrile (through C-alkyl malononitriles and 3,5-diamino-4-alkylpyrazoles) has been explored.Although some difficulties arise in the double-deamination step, the method has allowed the synthesis of 4-benzyl-and 4-phenyl-pyrazoles.New 3-halogenopyrazoles have also been prepared.The synthesis of 3,5-diamino-4-iodopyrazole is reported.This elusive compound has a 13C NMR spectrum in which an aromatic carbon (C-4) appears at δ 29,53.