Rungroj Saruengkhanphasit

Bangkok, 10210, Thailand

Last Updated: 09/26/2026

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Found 10 publications

Identification of antiproliferative nogalamycin series as potent inhibitors of EGFR tyrosine kinase: An in vitro and computational study.

Identification of antiproliferative nogalamycin series as potent inhibitors of EGFR tyrosine kinase: An in vitro and computational study.

Journal: Chemico-biological interactions

Published: January 27, 2026

Design, synthesis, in silico and in vitro evaluation of pyrrole-indole hybrids as dual tubulin and aromatase inhibitors with potent anticancer activities.

Design, synthesis, in silico and in vitro evaluation of pyrrole-indole hybrids as dual tubulin and aromatase inhibitors with potent anticancer activities.

Journal: RSC advances

Published: December 25, 2024

Metal- and photocatalyst-free approach to visible-light-induced acylation of quinoxalinones.

Metal- and photocatalyst-free approach to visible-light-induced acylation of quinoxalinones.

Journal: Organic & biomolecular chemistry

Published: May 03, 2024

Synthesis, in silico, in vitro evaluation of furanyl- and thiophenyl-3-phenyl-1H-indole-2-carbohydrazide derivatives as tubulin inhibitors and anticancer agents.

Synthesis, in silico, in vitro evaluation of furanyl- and thiophenyl-3-phenyl-1H-indole-2-carbohydrazide derivatives as tubulin inhibitors and anticancer agents.

Journal: RSC medicinal chemistry

Published: March 27, 2024

A structure-based virtual high-throughput screening, molecular docking, molecular dynamics and MM/PBSA study identified novel putative drug-like dual inhibitors of trypanosomal cruzain and rhodesain cysteine proteases.

A structure-based virtual high-throughput screening, molecular docking, molecular dynamics and MM/PBSA study identified novel putative drug-like dual inhibitors of trypanosomal cruzain and rhodesain cysteine proteases.

Journal: Molecular diversity

Published: September 05, 2022

Discovery of potent antiproliferative agents from selected oxygen heterocycles as EGFR tyrosine kinase inhibitors from the U.S. National Cancer Institute database by in silico screening and bioactivity evaluation.

Discovery of potent antiproliferative agents from selected oxygen heterocycles as EGFR tyrosine kinase inhibitors from the U.S. National Cancer Institute database by in silico screening and bioactivity evaluation.

Journal: Bioorganic & medicinal chemistry letters

Published: November 11, 2021

Visible-light-mediated decarboxylative alkylation of 2-pyridone derivatives via a C3-selective C-H functionalization.

Visible-light-mediated decarboxylative alkylation of 2-pyridone derivatives via a C3-selective C-H functionalization.

Journal: Organic & biomolecular chemistry

Published: October 14, 2021

Identification of new 3-phenyl-1H-indole-2-carbohydrazide derivatives and their structure-activity relationships as potent tubulin inhibitors and anticancer agents: A combined in silico, in vitro and synthetic study.

Identification of new 3-phenyl-1H-indole-2-carbohydrazide derivatives and their structure-activity relationships as potent tubulin inhibitors and anticancer agents: A combined in silico, in vitro and synthetic study.

Journal: Bioorganic chemistry

Published: December 30, 2020

Cascade oxime formation, cyclization to a nitrone, and intermolecular dipolar cycloaddition.

Cascade oxime formation, cyclization to a nitrone, and intermolecular dipolar cycloaddition.

Journal: Organic & biomolecular chemistry

Published: November 08, 2016

Synthesis of the tricyclic core of manzamine A.

Synthesis of the tricyclic core of manzamine A.

Journal: Organic & biomolecular chemistry

Published: February 04, 2015

Showing 1-10 of 10

Last Updated: 09/26/2026