A review on mechanistic insight of plant derived anticancer bioactive phytocompounds and their structure activity relationship

K Mazumder, A Aktar, P Roy, B Biswas, ME Hossain… - Molecules, 2022 - mdpi.com
Cancer is a disorder that rigorously affects the human population worldwide. There is a
steady demand for new remedies to both treat and prevent this life-threatening sickness due …

Naphthalene, a versatile platform in medicinal chemistry: sky-high perspective

S Makar, T Saha, SK Singh - European journal of medicinal chemistry, 2019 - Elsevier
Naphthalene, a cytotoxic moiety, is an extensively explored aromatic conjugated system with
applications in various pathophysiological conditions viz. anticancer, antimicrobial, anti …

Medicinal chemistry of combretastatin A4: present and future directions

GC Tron, T Pirali, G Sorba, F Pagliai… - Journal of medicinal …, 2006 - ACS Publications
A growing solid tumor relies on a develo** vasculature to meet its needs in terms of
oxygen, nutrients, depuration, etc. This implies that if the vascular bed that has developed …

Synthetic prodrug design enables biocatalytic activation in mice to elicit tumor growth suppression

I Nasibullin, I Smirnov, P Ahmadi, K Vong… - Nature …, 2022 - nature.com
Considering the intrinsic toxicities of transition metals, their incorporation into drug therapies
must operate at minimal amounts while ensuring adequate catalytic activity within complex …

Nickel (0)-catalyzed Heck cross-coupling via activation of aryl C–OPiv bonds

AR Ehle, Q Zhou, MP Watson - Organic letters, 2012 - ACS Publications
Using a Ni (dppf) catalyst generated in situ, Heck cross-coupling of aryl pivalates with a
variety of olefin partners has been accomplished. This method represents one of the first …

Discovery of 7-Hydroxy-6-methoxy-2-methyl-3-(3,4,5-trimethoxybenzoyl)benzo[b]furan (BNC105), a Tubulin Polymerization Inhibitor with Potent Antiproliferative and …

BL Flynn, GS Gill, DW Grobelny… - Journal of medicinal …, 2011 - ACS Publications
A structure–activity relationship (SAR) guided design of novel tubulin polymerization
inhibitors has resulted in a series of benzo [b] furans with exceptional potency toward cancer …

Highly potent triazole-based tubulin polymerization inhibitors

Q Zhang, Y Peng, XI Wang, SM Keenan… - Journal of medicinal …, 2007 - ACS Publications
We describe the synthesis and biological evaluation of a series of tubulin polymerization
inhibitors that contain the 1, 2, 4-triazole ring to retain the bioactive configuration afforded by …

[PDF][PDF] Combretastatin A-4 analogs as anticancer agents

A Chaudhary, SN Pandeya, P Kumar… - Mini reviews in …, 2007 - researchgate.net
Cornbretastatin A-4 (CA-4) is one of the most potent antinnitotic and antiangiogenic agents
of natural origin. It has displayed potent antitunnor effect in a wide variety of preclinical …

Substituted trans-Stilbenes, Including Analogues of the Natural Product Resveratrol, Inhibit the Human Tumor Necrosis Factor Alpha-Induced Activation of …

JJ Heynekamp, WM Weber, LA Hunsaker… - Journal of medicinal …, 2006 - ACS Publications
The transcription factor nuclear factor kappaB (NF-κB), which regulates expression of
numerous antiinflammatory genes as well as genes that promote development of the …

Development of combretastatins as potent tubulin polymerization inhibitors

SNA Bukhari, GB Kumar, HM Revankar, HL Qin - Bioorganic chemistry, 2017 - Elsevier
The combretastatins are isolated from South African tree combretum caffrum kuntze. The
lead compound combretastatin A-4 has displayed remarkable cytotoxic effect in a wide …