Design and synthesis of novel sulphamide tethered quinazolinone hybrids as potential antitumor agents-Reference-Cited by-同舟云学术

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Design and synthesis of novel sulphamide tethered quinazolinone hybrids as potential antitumor agents

Published:2019-04 Issue: Volume:1181 Page:403-411
ISSN:0022-2860
Container-title:Journal of Molecular Structure
language:en
Short-container-title:Journal of Molecular Structure

Author:

Venkatesh Ramineni,Kasaboina Suresh,Jain Nishant,Janardhan Sridhara,Holagunda Uma Devi,Nagarapu Lingaiah

Funder

Council of Scientific and Industrial Research, India

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Spectroscopy,Analytical Chemistry

Reference42 articles.

1. 1-Aminoacyl-2,3-dihydro-4(1H)-quinazolinone derivatives with choleretic and antifibrillatory activity

2. 4-Oxo-1,2,3,4-tetrahydroquinazolines. I. Syntheses and pharmacological properties of 2-methyl-3-aryl-4-oxo-1,2,3,4-tetrahydroquinazolines and their 1-acyl derivatives

3. Synthesis of 1,3-diamino-7,8,9,10-tetrahydropyrido[3,2-f]-quinazolines. Inhibitors ofCandida albicansdihydrofolate reductase as potential antifungal agents

4. Rational design of quinazoline-based irreversible inhibitors of human erythrocyte purine nucleoside phosphorylase

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