Moana Tercel
85 Park Rd
Grafton, AUK 1023, New Zealand
Grafton, AUK 1023, New Zealand
Last Updated: 09/26/2026
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Found 21 publications
Conjugation of Palbociclib with MHI-148 Has an Increased Cytotoxic Effect for Breast Cancer Cells and an Altered Mechanism of Action.
Journal: Molecules (Basel, Switzerland)
Published: November 25, 2021
Engineering the Escherichia coli Nitroreductase NfsA to Create a Flexible Enzyme-Prodrug Activation System.
Journal: Frontiers in pharmacology
Published: April 28, 2021
Spatially-resolved pharmacokinetic/pharmacodynamic modelling of bystander effects of a nitrochloromethylbenzindoline hypoxia-activated prodrug.
Journal: Cancer chemotherapy and pharmacology
Published: April 15, 2021
Antibody-Drug Conjugates Derived from Cytotoxic seco-CBI-Dimer Payloads Are Highly Efficacious in Xenograft Models and Form Protein Adducts In Vivo.
Journal: Bioconjugate chemistry
Published: April 11, 2019
Influence of a Basic Side Chain on the Properties of Hypoxia-Selective Nitro Analogues of the Duocarmycins: Demonstration of Substantial Anticancer Activity in Combination with Irradiation or Chemotherapy.
Journal: Journal of medicinal chemistry
Published: June 24, 2017
Analogues of DNA minor groove cross-linking agents incorporating aminoCBI, an amino derivative of the duocarmycins: Synthesis, cytotoxicity, and potential as payloads for antibody-drug conjugates.
Journal: Bioorganic & medicinal chemistry
Published: August 21, 2016
Mechanism of action of AminoCBIs: highly reactive but highly cytotoxic analogues of the duocarmycins.
Journal: Chembiochem : a European journal of chemical biology
Published: May 21, 2014
Preparation and properties of clickable amino analogues of the duocarmycins: factors that affect the efficiency of their fluorescent labelling of DNA.
Journal: ChemMedChem
Published: May 01, 2014
The flavoprotein FOXRED2 reductively activates nitro-chloromethylbenzindolines and other hypoxia-targeting prodrugs.
Journal: Biochemical pharmacology
Published: January 31, 2014
The cytotoxicity of duocarmycin analogues is mediated through alkylation of DNA, not aldehyde dehydrogenase 1: a comment.
Journal: Angewandte Chemie (International ed. in English)
Published: October 18, 2012
Last Updated: 09/26/2026