Molecular and Supramolecular Chemistry of Natural Products and Their Model Compounds By Jürgen-Hinrich Fuhrhop (Free University of Berlin) and Claus Endisch (Berlin, Germany). Marcel Dekker:  New York. 2000. x + 602 pp. $195.00. ISBN 0-8247-8201-1

2001 ◽  
Vol 123 (5) ◽  
pp. 1016-1016
Author(s):  
Karol S. Bruzik
Keyword(s):  
New York ◽  
Natural Products ◽  
Supramolecular Chemistry ◽  
Model Compounds ◽  
University Of Berlin

scholarly journals Asymmetric Synthesis and Cytotoxicity Evaluation of Right-Half Models of Antitumor Renieramycin Marine Natural Products

Marine Drugs ◽  
2018 ◽  
Vol 17 (1) ◽  
pp. 3 ◽  
Author(s):  
Takehiro Matsubara ◽  
Masashi Yokoya ◽  
Natchanun Sirimangkalakitti ◽  
Naoki Saito
Keyword(s):  
Prostate Cancer ◽  
Colorectal Cancer ◽  
Natural Products ◽  
Asymmetric Synthesis ◽  
Active Compound ◽  
Hct116 Cell ◽  
Human Prostate Cancer ◽  
Model Compounds ◽  
Structure Activity ◽  
Sar Study

A general protocol for the asymmetric synthesis of 3-N-arylmethylated right-half model compounds of renieramycins was developed, which enabled structure–activity relationship (SAR) study of several 3-N-arylmethyl derivatives. The most active compound (6a) showed significant cytotoxic activity against human prostate cancer DU145 and colorectal cancer HCT116 cell lines (IC50 = 11.9, and 12.5 nM, respectively).

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