A review on mechanistic insight of plant derived anticancer bioactive phytocompounds and their structure activity relationship
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 …
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
Naphthalene, a cytotoxic moiety, is an extensively explored aromatic conjugated system with
applications in various pathophysiological conditions viz. anticancer, antimicrobial, anti …
applications in various pathophysiological conditions viz. anticancer, antimicrobial, anti …
Medicinal chemistry of combretastatin A4: present and future directions
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 …
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
Considering the intrinsic toxicities of transition metals, their incorporation into drug therapies
must operate at minimal amounts while ensuring adequate catalytic activity within complex …
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
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 …
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 …
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 …
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 …
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 …
numerous antiinflammatory genes as well as genes that promote development of the …
Development of combretastatins as potent tubulin polymerization inhibitors
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 …
lead compound combretastatin A-4 has displayed remarkable cytotoxic effect in a wide …