Haikuo Ma

Jiangsu Key Laboratory Of Neuropsychiatric Diseases And College Of Pharmaceutical Sciences, 215123, PR China
Suzhou, Puerto Rico

Last Updated: 09/26/2026

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Found 18 publications

Synthesis and evaluation of dihydrofuro[2,3-b]pyridine derivatives as potent IRAK4 inhibitors.

Synthesis and evaluation of dihydrofuro[2,3-b]pyridine derivatives as potent IRAK4 inhibitors.

Journal: European journal of medicinal chemistry

Published: May 10, 2023

Synthesis and characterization of potent RIPK3 inhibitors based on a tricyclic scaffold.

Synthesis and characterization of potent RIPK3 inhibitors based on a tricyclic scaffold.

Journal: Future medicinal chemistry

Published: February 15, 2022

Design, synthesis, and evaluation of potent RIPK1 inhibitors with in vivo anti-inflammatory activity.

Design, synthesis, and evaluation of potent RIPK1 inhibitors with in vivo anti-inflammatory activity.

Journal: European journal of medicinal chemistry

Published: September 30, 2021

Ring closure strategy leads to potent RIPK3 inhibitors.

Ring closure strategy leads to potent RIPK3 inhibitors.

Journal: European journal of medicinal chemistry

Published: November 06, 2020

Design, synthesis, and evaluation of pyrrolidine based CXCR4 antagonists with in vivo anti-tumor metastatic activity.

Design, synthesis, and evaluation of pyrrolidine based CXCR4 antagonists with in vivo anti-tumor metastatic activity.

Journal: European journal of medicinal chemistry

Published: April 07, 2020

Design, synthesis, and evaluation of novel CXCR4 antagonists based on an aminoquinoline template.

Design, synthesis, and evaluation of novel CXCR4 antagonists based on an aminoquinoline template.

Journal: Bioorganic chemistry

Published: January 19, 2020

Structural optimization of aminopyrimidine-based CXCR4 antagonists.

Structural optimization of aminopyrimidine-based CXCR4 antagonists.

Journal: European journal of medicinal chemistry

Published: September 18, 2019

Structural optimization on a virtual screening hit of smoothened receptor.

Structural optimization on a virtual screening hit of smoothened receptor.

Journal: European journal of medicinal chemistry

Published: December 12, 2018

Discovery of potent and novel smoothened antagonists via structure-based virtual screening and biological assays.

Discovery of potent and novel smoothened antagonists via structure-based virtual screening and biological assays.

Journal: European journal of medicinal chemistry

Published: February 26, 2018

Design, synthesis, and structure-activity-relationship of a novel series of CXCR4 antagonists.

Design, synthesis, and structure-activity-relationship of a novel series of CXCR4 antagonists.

Journal: European journal of medicinal chemistry

Published: December 20, 2017

Discovery and characterization of a potent Wnt and hedgehog signaling pathways dual inhibitor.

Discovery and characterization of a potent Wnt and hedgehog signaling pathways dual inhibitor.

Journal: European journal of medicinal chemistry

Published: August 18, 2017

Design, synthesis, and evaluation of novel porcupine inhibitors featuring a fused 3-ring system based on the 'reversed' amide scaffold.

Design, synthesis, and evaluation of novel porcupine inhibitors featuring a fused 3-ring system based on the 'reversed' amide scaffold.

Journal: Bioorganic & medicinal chemistry

Published: July 20, 2016

Showing 1-12 of 18

Last Updated: 09/26/2026