Indole: A privileged scaffold for the design of anti-cancer agents
Y Wan, Y Li, C Yan, M Yan, Z Tang - European journal of medicinal …, 2019 - Elsevier
In general, heterocyclic compounds are a significant source of pharmacologically active
compounds. Among them, the indole scaffold widely distributes in natural products and …
compounds. Among them, the indole scaffold widely distributes in natural products and …
Natural products and their derivatives: Promising modulators of tumor immunotherapy
LJ Deng, M Qi, N Li, YH Lei, DM Zhang… - Journal of Leucocyte …, 2020 - academic.oup.com
A wealth of evidence supports the role of tumor immunotherapy as a vital therapeutic option
in cancer. In recent decades, accumulated studies have revealed the anticancer activities of …
in cancer. In recent decades, accumulated studies have revealed the anticancer activities of …
Characterization and heterologous reconstitution of Taxus biosynthetic enzymes leading to baccatin III
B Jiang, L Gao, H Wang, Y Sun, X Zhang, H Ke, S Liu… - Science, 2024 - science.org
Paclitaxel is a well known anticancer compound. Its biosynthesis involves the formation of a
highly functionalized diterpenoid core skeleton (baccatin III) and the subsequent assembly …
highly functionalized diterpenoid core skeleton (baccatin III) and the subsequent assembly …
Engineering a second‐order DNA logic‐gated nanorobot to sense and release on live cell membranes for multiplexed diagnosis and synergistic therapy
Tumor biomarker‐based theranostics have achieved broad interest and success in recent
years. However, single biomarker‐based recognition can cause false‐positive feedback …
years. However, single biomarker‐based recognition can cause false‐positive feedback …
Molecular interactions at the colchicine binding site in tubulin: An X-ray crystallography perspective
Highlights•Colchicine binding site inhibitors (CBSIs) emerge as new generations of tubulin
inhibitors.•CBSIs are less susceptible to multidrug resistance than FDA-approved tubulin …
inhibitors.•CBSIs are less susceptible to multidrug resistance than FDA-approved tubulin …
Sequential doxycycline and colchicine combination therapy in Covid-19: the salutary effects
Abstract Coronavirus virus disease 2019 (COVID-19) is a viral infectious disease caused by
the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), actually considered as …
the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), actually considered as …
Role of indole scaffolds as pharmacophores in the development of anti-lung cancer agents
Lung cancer is the leading cause of death in men and women worldwide, affecting millions
of people. Between the two types of lung cancers, non-small cell lung cancer (NSCLC) is …
of people. Between the two types of lung cancers, non-small cell lung cancer (NSCLC) is …
[HTML][HTML] New insights into the anticancer therapeutic potential of maytansine and its derivatives
Maytansine is a pharmacologically active 19-membered ansamacrolide derived from
various medicinal plants and microorganisms. Among the most studied pharmacological …
various medicinal plants and microorganisms. Among the most studied pharmacological …
Perspectives and mechanisms for targeting mitotic catastrophe in cancer treatment
Z Bai, Y Zhou, Y Peng, X Ye, L Ma - … et Biophysica Acta (BBA)-Reviews on …, 2023 - Elsevier
Mitotic catastrophe is distinct from other cell death modes due to unique nuclear alterations
characterized as multi and/or micronucleation. Mitotic catastrophe is a common and virtually …
characterized as multi and/or micronucleation. Mitotic catastrophe is a common and virtually …
Recent progress on microtubule degradation agents
C Zhang, M Zhao, G Wang, Y Li - Journal of Medicinal Chemistry, 2023 - ACS Publications
Targeted protein degradation (TPD) has emerged as the most promising approach for the
specific knockdown of disease-associated proteins and is achieved by exploiting the cellular …
specific knockdown of disease-associated proteins and is achieved by exploiting the cellular …