Qiu-qin He

2005 Songhu Road
Yangpu, China

Last Updated: 09/26/2026

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Found 17 publications

Synthesis of furoquinolines from 2-alkenylanilines via anodic dearomatization and cascade cyclization.

Synthesis of furoquinolines from 2-alkenylanilines via anodic dearomatization and cascade cyclization.

Journal: Organic & biomolecular chemistry

Published: April 24, 2026

Synthesis of 4-amino-7-oxyindoles via dearomatization of 4-alkyl-2-alkynylanilines and dual fragment incorporation with O-benzoylhydroxylamines.

Synthesis of 4-amino-7-oxyindoles via dearomatization of 4-alkyl-2-alkynylanilines and dual fragment incorporation with O-benzoylhydroxylamines.

Journal: Organic & biomolecular chemistry

Published: January 12, 2026

Identification of CH2-linker modified desfluoroquinolone-aminopyrimidine hybrids to combat antibiotic-resistant gram-positive bacteria.

Identification of CH2-linker modified desfluoroquinolone-aminopyrimidine hybrids to combat antibiotic-resistant gram-positive bacteria.

Journal: Bioorganic chemistry

Published: January 26, 2025

Identification of CH2-linked quinolone-aminopyrimidine hybrids as potent anti-MRSA agents: Low resistance potential and lack of cross-resistance with fluoroquinolone antibiotics.

Identification of CH2-linked quinolone-aminopyrimidine hybrids as potent anti-MRSA agents: Low resistance potential and lack of cross-resistance with fluoroquinolone antibiotics.

Journal: European journal of medicinal chemistry

Published: February 18, 2024

Indole derivatives as tubulin polymerization inhibitors for the development of promising anticancer agents.

Indole derivatives as tubulin polymerization inhibitors for the development of promising anticancer agents.

Journal: Bioorganic & medicinal chemistry

Published: October 29, 2021

Advances in the development of HIV integrase strand transfer inhibitors.

Advances in the development of HIV integrase strand transfer inhibitors.

Journal: European journal of medicinal chemistry

Published: May 01, 2021

Design and synthesis of novel desfluoroquinolone-aminopyrimidine hybrids as potent anti-MRSA agents with low hERG activity.

Design and synthesis of novel desfluoroquinolone-aminopyrimidine hybrids as potent anti-MRSA agents with low hERG activity.

Journal: Bioorganic chemistry

Published: May 27, 2020

Structural Modifications of Diarylpyrimidine-quinolone Hybrids as Potent HIV-1 NNRTIs with an Improved Drug Resistance Profile.

Structural Modifications of Diarylpyrimidine-quinolone Hybrids as Potent HIV-1 NNRTIs with an Improved Drug Resistance Profile.

Journal: Current pharmaceutical design

Published: January 07, 2016

Anti-HIV diarylpyrimidine-quinolone hybrids and their mode of action.

Anti-HIV diarylpyrimidine-quinolone hybrids and their mode of action.

Journal: Bioorganic & medicinal chemistry

Published: February 24, 2015

Synthesis and biological evaluation of DAPY-DPEs hybrids as non-nucleoside inhibitors of HIV-1 reverse transcriptase.

Synthesis and biological evaluation of DAPY-DPEs hybrids as non-nucleoside inhibitors of HIV-1 reverse transcriptase.

Journal: Bioorganic & medicinal chemistry

Published: October 21, 2014

Docking-based CoMFA and CoMSIA studies on naphthyl-substituted diarylpyrimidines as NNRTIs.

Docking-based CoMFA and CoMSIA studies on naphthyl-substituted diarylpyrimidines as NNRTIs.

Journal: SAR and QSAR in environmental research

Published: September 23, 2014

Synthesis and biological evaluation of CHX-DAPYs as HIV-1 non-nucleoside reverse transcriptase inhibitors.

Synthesis and biological evaluation of CHX-DAPYs as HIV-1 non-nucleoside reverse transcriptase inhibitors.

Journal: Bioorganic & medicinal chemistry

Published: February 12, 2014

Showing 1-12 of 17

Last Updated: 09/26/2026