Quantitative electronic structure-activity relationship (QESAR) of natural cytotoxic compounds: maytansinoids, quassinoids and cucurbitacins-Reference-Cited by-同舟云学术

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Quantitative electronic structure-activity relationship (QESAR) of natural cytotoxic compounds: maytansinoids, quassinoids and cucurbitacins

Published:1994-12 Issue:5-6 Volume:2 Page:331-350
ISSN:0928-0987
Container-title:European Journal of Pharmaceutical Sciences
language:en
Short-container-title:European Journal of Pharmaceutical Sciences

Author:

Dang Giap van,Rode Bernd M.,Stuppner Hermann

Publisher

Elsevier BV

Subject

Pharmaceutical Science

Reference53 articles.

1. Molecular Modelling Software;Alchemy,1988

2. In VitroCytotoxicity of a Series of Quassinoids fromBrucea javanicaFruits Against KB Cells

3. Plant Anticancer Agents. XXIII. 6α-Senecioyloxychaparrin, A New Antileukemic Quassinoid From Simaba multiflora

4. Isolation, chemical characterization and structure of ansamitocin, a new antitumor ansamycin antibiotic

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1. Anti-Diabetic Effects of Cucurbitacins from Ibervillea lindheimeri on Induced Mouse Diabetes;Journal of Chemistry;2022-06-25

2. Multivariate SAR and QSAR of cucurbitacin derivatives as cytotoxic compounds in a human lung adenocarcinoma cell line;Journal of Molecular Graphics and Modelling;2014-03

3. Terpenes;Lead Compounds from Medicinal Plants for the Treatment of Cancer;2013

4. Quassinoids: Chemistry and Novel Detection Techniques;Natural Products;2013

5. Synthesis and cytotoxic activity evaluation of dihydrocucurbitacin B and cucurbitacin B derivatives;Bioorganic & Medicinal Chemistry;2012-05

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