Tubulin as a target for anticancer drugs: agents which interact with the mitotic spindle

A Jordan, JA Hadfield, NJ Lawrence… - Medicinal research …, 1998 - Wiley Online Library
Tubulin is the biochemical target for several clinically used anticancer drugs, including
paclitaxel and the vinca alkaloids vincristine and vinblastine. This review describes both the …

Exploring the boundaries of “practical”: de novo syntheses of complex natural product-based drug candidates

TK Allred, F Manoni, PG Harran - Chemical Reviews, 2017 - ACS Publications
This review examines the state of the art in synthesis as it relates to the building of complex
architectures on scales sufficient to drive human drug trials. We focus on the relatively few …

[图书][B] Anticancer agents from natural products

GM Cragg, DGI Kingston, DJ Newman - 2005 - taylorfrancis.com
Plants, marine organisms, and microorganisms have evolved complex chemical defense
and signaling systems that are designed to protect them from predators and provide other …

Biosynthetic Characterization and Chemoenzymatic Assembly of the Cryptophycins. Potent Anticancer Agents from Nostoc Cyanobionts

NA Magarvey, ZQ Beck, T Golakoti, Y Ding… - ACS chemical …, 2006 - ACS Publications
The lichen cyanobacterial symbiont Nostoc sp. ATCC 53789 and its close relative Nostoc sp.
GSV 224 are prolific producers of natural products, generating> 25 derivatives of the …

The cryptophycins: their synthesis and anticancer activity

MJ Eggen, GI Georg - Medicinal research reviews, 2002 - Wiley Online Library
The cryptophycins are a unique family of 16‐membered macrolide antimitotic agents
isolated from the cyanobacteria Nostoc sp. Their molecular target is tubulin protein wherein …

Small molecule modulators of protein–protein interactions: selected case studies

M Aeluri, S Chamakuri, B Dasari, SKR Guduru… - Chemical …, 2014 - ACS Publications
There is growing interest within the pharmaceutical community to undertake biological
targets that involve protein− protein 1 and, in general, biomacromolecular interactions 2 (PPI …

Antimitotic peptides and depsipeptides

E Hamel, DG Covell - Current Medicinal Chemistry-Anti-Cancer …, 2002 - ingentaconnect.com
Tubulin is the target for an ever increasing number of unusual peptides and depsipeptides
that were originally isolated from a wide variety of organisms. Since tubulin is the major …

Enantioselective synthesis of (+)-cryptophycin 52 (LY355703), a potent antimitotic antitumor agent

AK Ghosh, L Swanson - The Journal of Organic Chemistry, 2003 - ACS Publications
A highly enantioselective and convergent synthesis of cryptophycin 52 (2), an exceedingly
potent cytotoxic agent, is described. Cryptophycin 52, a synthetic variant of the cryptophycin …

Chemoenzymatic synthesis of cryptophycin/arenastatin natural products

ZQ Beck, CC Aldrich, NA Magarvey, GI Georg… - Biochemistry, 2005 - ACS Publications
Microbially derived modular polyketide synthase and nonribosomal peptide synthetase
biosynthetic pathways are a rich source of novel natural products. Development of these …

Synthesis of cryptophycin 52 using the Sharpless asymmetric dihydroxylation: diol to epoxide transformation optimized for a base-sensitive substrate

J Liang, ED Moher, RE Moore… - The Journal of Organic …, 2000 - ACS Publications
A synthesis of cryptophycin 52 (2) is reported using a Sharpless asymmetric dihydroxylation
(AD) strategy to install the epoxide moiety. The high stereoselectivity of the AD reaction that …