Zhu-ping Xiao

Hunan Provincial Key Laboratory Of Research, Hunan Engineering Laboratory For Analyse And Drugs Development Of Ethnomedicine In Wuling Mountains, Jishou 416000, PR China
Puerto Rico

Last Updated: 09/26/2026

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Found 26 publications

Synthesis and evaluation of 5-phenoxylmethyl-1,3,4-oxadiazol-2-ones/oxadiazole-2-thiones as potent urease inhibitors.

Synthesis and evaluation of 5-phenoxylmethyl-1,3,4-oxadiazol-2-ones/oxadiazole-2-thiones as potent urease inhibitors.

Journal: Bioorganic & medicinal chemistry

Published: September 12, 2025

Novel sulfamide-hydroxamic acids containing piperazine/piperidine segment as potent urease inhibitors: Synthesis, biological evaluation, kinetics and molecular docking studies.

Novel sulfamide-hydroxamic acids containing piperazine/piperidine segment as potent urease inhibitors: Synthesis, biological evaluation, kinetics and molecular docking studies.

Journal: Bioorganic & medicinal chemistry

Published: March 05, 2025

Synthesis and biological evaluation of triazolones/oxadiazolones as novel urease inhibitors.

Synthesis and biological evaluation of triazolones/oxadiazolones as novel urease inhibitors.

Journal: Bioorganic & medicinal chemistry

Published: December 05, 2023

Identification of (N-aryl-N-arylsulfonyl)aminoacetohydroxamic acids as novel urease inhibitors and the mechanism exploration.

Identification of (N-aryl-N-arylsulfonyl)aminoacetohydroxamic acids as novel urease inhibitors and the mechanism exploration.

Journal: Bioorganic chemistry

Published: September 28, 2022

Synthesis, evaluation and mechanism exploration of 2-(N-(3-nitrophenyl)-N-phenylsulfonyl)aminoacetohydroxamic acids as novel urease inhibitors.

Synthesis, evaluation and mechanism exploration of 2-(N-(3-nitrophenyl)-N-phenylsulfonyl)aminoacetohydroxamic acids as novel urease inhibitors.

Journal: Bioorganic & medicinal chemistry letters

Published: September 14, 2022

Identification, potency evaluation, and mechanism clarification of α-glucosidase inhibitors from tender leaves of Lithocarpus polystachyus Rehd.

Identification, potency evaluation, and mechanism clarification of α-glucosidase inhibitors from tender leaves of Lithocarpus polystachyus Rehd.

Journal: Food chemistry

Published: June 28, 2021

N-monosubstituted thiosemicarbazide as novel Ure inhibitors: synthesis, biological evaluation and molecular docking.

N-monosubstituted thiosemicarbazide as novel Ure inhibitors: synthesis, biological evaluation and molecular docking.

Journal: Future medicinal chemistry

Published: September 07, 2020

N-monoarylacetothioureas as potent urease inhibitors: synthesis, SAR, and biological evaluation.

N-monoarylacetothioureas as potent urease inhibitors: synthesis, SAR, and biological evaluation.

Journal: Journal of enzyme inhibition and medicinal chemistry

Published: December 28, 2019

The synthesis and evaluation of phenoxyacylhydroxamic acids as potential agents for Helicobacter pylori infections.

The synthesis and evaluation of phenoxyacylhydroxamic acids as potential agents for Helicobacter pylori infections.

Journal: Bioorganic & medicinal chemistry

Published: June 04, 2018

Arylamino containing hydroxamic acids as potent urease inhibitors for the treatment of Helicobacter pylori infection.

Arylamino containing hydroxamic acids as potent urease inhibitors for the treatment of Helicobacter pylori infection.

Journal: European journal of medicinal chemistry

Published: April 27, 2018

Resolution and evaluation of 3-chlorophenyl-3-hydroxypropionylhydroxamic acid as antivirulence agent with excellent eradication efficacy in Helicobacter pylori infected mice.

Resolution and evaluation of 3-chlorophenyl-3-hydroxypropionylhydroxamic acid as antivirulence agent with excellent eradication efficacy in Helicobacter pylori infected mice.

Journal: European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences

Published: March 07, 2018

Synthesis and evaluation of adenosine containing 3-arylfuran-2(5H)-ones as tyrosyl-tRNA synthetase inhibitors.

Synthesis and evaluation of adenosine containing 3-arylfuran-2(5H)-ones as tyrosyl-tRNA synthetase inhibitors.

Journal: European journal of medicinal chemistry

Published: November 04, 2016

Showing 1-12 of 26

Last Updated: 09/26/2026