Cytotoxic and antiproliferative activity of thiazole derivatives of Ochraceolide A

Pentacyclic Triterpenoids with Nitrogen-Containing Heterocyclic Moiety, Privileged Hybrids in Anticancer Drug Discovery

(2021) Vuyolwethu Khwaza et al.   MOLECULES

Single- and Two-Electron Reduction of Nitroaromatic Compounds by Flavoenzymes: Mechanisms and Implications for Cytotoxicity

(2021) Narimantas Čėnas et al.   INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

Natural Products as Sources of New Drugs over the Nearly Four Decades from 01/1981 to 09/2019

(2020) David J. Newman et al.   JOURNAL OF NATURAL PRODUCTS

Nitrofuran drugs beyond redox cycling: Evidence of Nitroreduction-independent cytotoxicity mechanism

(2020) C. Gallardo-Garrido et al.   TOXICOLOGY AND APPLIED PHARMACOLOGY

Synthesis and biological evaluation of triterpenoid thiazoles derived from betulonic acid, dihydrobetulonic acid, and ursonic acid

(2019) Lucie Borková et al.   EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY

Synthesis, structure analysis and activity against breast and cervix cancer cells of a triterpenoid thiazole derived from ochraceolide A

(2019) A.D. Herrera-España et al.   JOURNAL OF MOLECULAR STRUCTURE

Estimating the global cancer incidence and mortality in 2018: GLOBOCAN sources and methods

(2018) J. Ferlay et al.   INTERNATIONAL JOURNAL OF CANCER

Oleanane-, ursane-, and quinone methide friedelane-type triterpenoid derivatives: Recent advances in cancer treatment

(2017) Jorge A.R. Salvador et al.   EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY

Pentacyclic triterpenoids with nitrogen- and sulfur-containing heterocycles: synthesis and medicinal significance

(2015) Miroslav Kvasnica et al.   NATURAL PRODUCT REPORTS

Cytotoxic heterocyclic triterpenoids derived from betulin and betulinic acid

(2012) Milan Urban et al.   BIOORGANIC & MEDICINAL CHEMISTRY

Pentacyclic Triterpenes of the Lupane, Oleanane and Ursane Group as Tools in Cancer Therapy

(2009) Melanie Laszczyk   PLANTA MEDICA

Preliminary evaluation of the toxicity of some synthetic furan derivatives in two cell lines andArtemia salina

(2008) María I. Amaro et al.   JOURNAL OF APPLIED TOXICOLOGY