Recent advances in microtubule-stabilizing agents
YN Cao, LL Zheng, D Wang, XX Liang, F Gao… - European journal of …, 2018 - Elsevier
Highly dynamic mitotic spindle microtubules are superb therapeutic targets for a group of
chemically diverse and clinically successful anticancer drugs. Microtubule-targeted drugs …
chemically diverse and clinically successful anticancer drugs. Microtubule-targeted drugs …
Mitotic poisons in research and medicine
J Škubník, M Jurášek, T Ruml, S Rimpelová - Molecules, 2020 - mdpi.com
Cancer is one of the greatest challenges of the modern medicine. Although much effort has
been made in the development of novel cancer therapeutics, it still remains one of the most …
been made in the development of novel cancer therapeutics, it still remains one of the most …
Marine invertebrate natural products that target microtubules
JH Miller, JJ Field, A Kanakkanthara… - Journal of natural …, 2018 - ACS Publications
Marine natural products as secondary metabolites are a potential major source of new drugs
for treating disease. In some cases, cytotoxic marine metabolites target the microtubules of …
for treating disease. In some cases, cytotoxic marine metabolites target the microtubules of …
Natural product analogues: towards a blueprint for analogue-focused synthesis
MWP Bebbington - Chemical Society Reviews, 2017 - pubs.rsc.org
For the first time a general overview of approaches to the synthesis of natural product
analogues is presented. This reflects a process of evolution of natural product synthesis …
analogues is presented. This reflects a process of evolution of natural product synthesis …
Peloruside A: A lead non-taxoid-site microtubule-stabilizing agent with potential activity against cancer, neurodegeneration, and autoimmune disease
A Kanakkanthara, PT Northcote, JH Miller - Natural product reports, 2016 - pubs.rsc.org
Covering: 2000 up to 2016 Peloruside A, a macrocyclic secondary metabolite from a New
Zealand marine sponge, Mycale hentscheli, has shown potent antiproliferative activity in …
Zealand marine sponge, Mycale hentscheli, has shown potent antiproliferative activity in …
Gracilin a derivatives target early events in alzheimer's disease: in vitro effects on neuroinflammation and oxidative stress
R Alvariño, E Alonso, ME Abbasov… - ACS chemical …, 2019 - ACS Publications
The search for compounds capable of targeting early pathological changes of Alzheimer̀s
disease (AD), such as oxidative stress and neuroinflammation, is an important challenge …
disease (AD), such as oxidative stress and neuroinflammation, is an important challenge …
Applications of the dess-martin oxidation in total synthesis of natural products
MM Heravi, T Momeni, V Zadsirjan… - Current Organic …, 2021 - ingentaconnect.com
Dess–Martin periodinane (DMP), a commercially available chemical, is frequently utilized as
a mild oxidative agent for the selective oxidation of primary and secondary alcohols to their …
a mild oxidative agent for the selective oxidation of primary and secondary alcohols to their …
Stereoselective Synthesis of the C9–C19 Fragment of Peloruside A
SCD Kennington, JM Romo, P Romea, F Urpi - Organic letters, 2016 - ACS Publications
A concise synthesis of the C9–C19 fragment of peloruside A that is both highly
stereoselective and efficient is described. Achieving an overall yield of 23% over 14 steps …
stereoselective and efficient is described. Achieving an overall yield of 23% over 14 steps …
The chemistry of the carbon-transition metal double and triple bond: Annual survey covering the year 2015
JW Herndon - Coordination Chemistry Reviews, 2016 - Elsevier
This is a review of papers published in the year 2015 that focus on the synthesis, reactivity,
or properties of compounds containing a carbon-transition metal double or triple bond …
or properties of compounds containing a carbon-transition metal double or triple bond …
Selective synthesis of unsymmetrical aliphatic acyloins through oxidation of iridium enolates
A Sanz‐Marco, S Martinez‐Erro… - … –A European Journal, 2018 - Wiley Online Library
The first method to access unsymmetrical aliphatic acyloins is presented. The method relies
on a fast 1, 3‐hydride shift mediated by an IrIII complex in allylic alcohols followed by …
on a fast 1, 3‐hydride shift mediated by an IrIII complex in allylic alcohols followed by …