[HTML][HTML] Antibody–drug conjugates: Recent advances in payloads

Z Wang, H Li, L Gou, W Li, Y Wang - Acta Pharmaceutica Sinica B, 2023 - Elsevier
Abstract Antibody‒drug conjugates (ADCs), which combine the advantages of monoclonal
antibodies with precise targeting and payloads with efficient killing, show great clinical …

Biosynthesis of cyclopropane in natural products

S Ma, D Mandalapu, S Wang, Q Zhang - Natural Product Reports, 2022 - pubs.rsc.org
Covering: 2012 to 2021 Cyclopropane attracts wide interests in the fields of synthetic and
pharmaceutical chemistry, and chemical biology because of its unique structural and …

The human gut bacterial genotoxin colibactin alkylates DNA

MR Wilson, Y Jiang, PW Villalta, A Stornetta… - Science, 2019 - science.org
INTRODUCTION Members of the human gut microbiota have been implicated in the
development and progression of colorectal cancer (CRC). These CRC-associated …

Design, synthesis, and evaluation of linker-duocarmycin payloads: toward selection of HER2-targeting antibody–drug conjugate SYD985

RC Elgersma, RGE Coumans, T Huijbregts… - Molecular …, 2015 - ACS Publications
Antibody–drug conjugates (ADCs) that are currently on the market or in clinical trials are
predominantly based on two drug classes: auristatins and maytansinoids. Both are tubulin …

Antibody drug conjugates for treatment of breast cancer: novel targets and diverse approaches in ADC design

PA Trail, GM Dubowchik, TB Lowinger - Pharmacology & therapeutics, 2018 - Elsevier
Breast cancer is a heterogeneous group of malignancies with a spectrum of molecular
subtypes, pathologies and outcomes that together comprise the most common non …

Aldehyde dehydrogenases in cancer: an opportunity for biomarker and drug development?

K Pors, JS Moreb - Drug discovery today, 2014 - Elsevier
Highlights•High ALDH expression in CSCs is associated with a worse prognosis.•ALDH
isozyme expression can to some extent be cancer specific.•Rational approach to chemical …

40 years of duocarmycins: a graphical structure/function review of their chemical evolution, from SAR to prodrugs and ADCs

JG Felber, O Thorn-Seshold - JACS Au, 2022 - ACS Publications
Synthetic analogues of the DNA-alkylating cytotoxins of the duocarmycin class have been
extensively investigated in the past 40 years, driven by their high potency, their unusual …

Intratumoural cytochrome P450 expression in breast cancer: impact on standard of care treatment and new efforts to develop tumour-selective therapies

S Sneha, SC Baker, A Green, S Storr, R Aiyappa… - Biomedicines, 2021 - mdpi.com
Despite significant advances in treatment strategies over the past decade, selective
treatment of breast cancer with limited side-effects still remains a great challenge. The …

Reactivity of an unusual amidase may explain colibactin's DNA cross-linking activity

Y Jiang, A Stornetta, PW Villalta… - Journal of the …, 2019 - ACS Publications
Certain commensal and pathogenic bacteria produce colibactin, a small-molecule genotoxin
that causes interstrand cross-links in host cell DNA. Although colibactin alkylates DNA, the …

Prodrugs for targeted tumor therapies: recent developments in ADEPT, GDEPT and PMT

LF Tietze, K Schmuck - Current pharmaceutical design, 2011 - ingentaconnect.com
The treatment of cancer with common anti-proliferative agents generally suffers from an
insufficient differentiation between normal and malignant cells which results in extensive …