Rational approaches, design strategies, structure activity relationship and mechanistic insights for anticancer hybrids

K Nepali, S Sharma, M Sharma, PMS Bedi… - European journal of …, 2014 - Elsevier
A Hybrid drug which comprises the incorporation of two drug pharmacophores in one single
molecule are basically designed to interact with multiple targets or to amplify its effect …

A review: Biologically active 3, 4-heterocycle-fused coumarins

F Salehian, H Nadri, L Jalili-Baleh… - European Journal of …, 2021 - Elsevier
The combination of heterocycles offers a new opportunity to create novel multicyclic
compounds having improved biological activity. Coumarins are ubiquitous natural …

Lamellarins and related pyrrole-derived alkaloids from marine organisms

H Fan, J Peng, MT Hamann, JF Hu - Chemical reviews, 2008 - ACS Publications
Marine organisms have proven to be rich sources of unique alkaloids. In earlier surveys we
comprehensively reviewed several intriguing groups of marine alkaloids, including the …

Synthesis and biological activity of pyrrole, pyrroline and pyrrolidine derivatives with two aryl groups on adjacent positions

F Bellina, R Rossi - Tetrahedron, 2006 - Elsevier
Five-membered heterocycle derivatives with two aryl groups on adjacent positions include
several classes of natural and unnatural compounds that exhibit a variety of biological and …

[HTML][HTML] Overview of P-glycoprotein inhibitors: a rational outlook

KMR Srivalli, PK Lakshmi - Brazilian Journal of Pharmaceutical …, 2012 - SciELO Brasil
P-glycoprotein (P-gp), a transmembrane permeability glycoprotein, is a member of ATP
binding cassette (ABC) super family that functions specifically as a carrier mediated primary …

Marine natural products

JW Blunt, BR Copp, WP Hu, MHG Munro… - Natural product …, 2007 - pubs.rsc.org
Covering: 2005. Previous review: Nat. Prod. Rep., 2006, 23, 26 This review covers the
literature published in 2005 for marine natural products, with 704 citations (493 for the …

Natural alkaloids as P-gp inhibitors for multidrug resistance reversal in cancer

P Joshi, RA Vishwakarma, SB Bharate - European journal of medicinal …, 2017 - Elsevier
The biggest challenge associated with cancer chemotherapy is the development of cross
multi-drug resistance to almost all anti-cancer agents upon chronic treatment. The major …

Anticancer properties of lamellarins

C Bailly - Marine Drugs, 2015 - mdpi.com
In 1985 the first lamellarins were isolated from a small oceanic sea snail. Today, more than
50 lamellarins have been inventoried and numerous derivatives synthesized and tested as …

Revisiting the ABCs of multidrug resistance in cancer chemotherapy

AK Tiwari, K Sodani, CL Dai… - Current …, 2011 - ingentaconnect.com
The adenosine triphosphate binding cassette (ABC) transporters are one of the largest
transmembrane gene families in humans. The ABC transporters are present in a number of …

Molecular determinants of topoisomerase I poisoning by Lamellarins: Comparison with Camptothecin and structure− activity relationships

E Marco, W Laine, C Tardy, A Lansiaux… - Journal of medicinal …, 2005 - ACS Publications
A series of lamellarin derivatives have been studied as topoisomerase I (Top1) inhibitors.
Molecular models of the ternary complexes formed between the DNA-Top1 ensemble and …