about
Structural analysis of inhibition of E. coli methionine aminopeptidase: implication of loop adaptability in selective inhibition of bacterial enzymesSynthesis, biological evaluation, and structure-activity relationships of N-benzoyl-2-hydroxybenzamides as agents active against P. falciparum (K1 strain), Trypanosomes, and Leishmania.Novel N-benzoyl-2-hydroxybenzamide disrupts unique parasite secretory pathway.Novel DNA Polymer for Amplification Pretargeting.Suzuki coupling based synthesis and in vitro cytotoxic evaluation of 7-heteroaryl-substituted camptothecin analogs.Synthesis and biological evaluation of new homocamptothecin analogs.Identification, synthesis, and pharmacological evaluation of tetrahydroindazole based ligands as novel antituberculosis agents.From serendipity to rational antituberculosis drug discovery of mefloquine-isoxazole carboxylic acid esters.Searching for new cures for tuberculosis: design, synthesis, and biological evaluation of 2-methylbenzothiazoles.The discovery and optimization of novel dual inhibitors of topoisomerase II and histone deacetylase.Identification of potent type I MetAP inhibitors by simple bioisosteric replacement. Part 1: Synthesis and preliminary SAR studies of thiazole-4-carboxylic acid thiazol-2-ylamide derivatives.Identification of potent type I MetAPs inhibitors by simple bioisosteric replacement. Part 2: SAR studies of 5-heteroalkyl substituted TCAT derivatives.Total synthesis of camptothecin and SN-38
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description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Qingqing Huang
@ast
Qingqing Huang
@en
Qingqing Huang
@es
Qingqing Huang
@nl
Qingqing Huang
@sl
type
label
Qingqing Huang
@ast
Qingqing Huang
@en
Qingqing Huang
@es
Qingqing Huang
@nl
Qingqing Huang
@sl
prefLabel
Qingqing Huang
@ast
Qingqing Huang
@en
Qingqing Huang
@es
Qingqing Huang
@nl
Qingqing Huang
@sl
P1053
M-6824-2013
P106
P31
P3829
P496
0000-0001-7080-7588