New Type of Febrifugine Analogues, Bearing a Quinolizidine Moiety, Show Potent Antimalarial Activity against Plasmodium Malaria Parasite-Reference-Cited by-同舟云学术

New Type of Febrifugine Analogues, Bearing a Quinolizidine Moiety, Show Potent Antimalarial Activity against Plasmodium Malaria Parasite

Published:1999-07-27 Issue:16 Volume:42 Page:3163-3166
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Takaya Yoshiaki¹,Tasaka Hidehisa¹,Chiba Tomoyuki¹,Uwai Koji¹,Tanitsu Masa-aki¹,Kim Hye-Sook¹,Wataya Yusuke¹,Miura Masatomo¹,Takeshita Mitsuhiro¹,Oshima Yoshiteru¹

Affiliation:

1. Graduate School of Pharmaceutical Sciences, Tohoku University, Aoba-yama, Sendai 980-8578, Japan, Faculty of Pharmaceutical Sciences, Okayama University, Tsushima, Okayama 700-8530, Japan, and Tohoku College of Pharmacy, Komatsushima, Sendai 981-8558, Japan

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm990131e

Reference10 articles.

1. Alkaloids of Dichroa febrifuga. I. Isolation and Degradative Studies

2. Stereochemistry of febrifugine. II. Evidence for the trans configuration in the piperidine ring

3. An Antimalarial Alkaloid from Hydrangea

Cited by 147 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Novel quinazolines bearing 1,3,4-thiadiazole-aryl urea derivative as anticancer agents: design, synthesis, molecular docking, DFT and bioactivity evaluations;BMC Chemistry;2024-02-12

2. A Novel Bibenzyl Derivative of Hydrangea chinensis;Chemistry of Natural Compounds;2024-01

3. Targeting Aminoacyl tRNA Synthetases for Antimalarial Drug Development;Annual Review of Microbiology;2023-09-15

4. Copper-Catalyzed Consecutive Ullmann, Decarboxylation, Oxidation, and Dehydration Reaction for Synthesis of Pyrrolo or Pyrido[1,2-a]imidazo[1,2-c]quinazolines;Organic Letters;2023-06-29

5. 3a-(4-Chlorophenyl)-1-methyl-3a,4-dihydroimidazo[1,5-a]quinazolin-5(3H)-one: Synthesis and In Silico Evaluation as a Ligand in the µ-Opioid Receptor;Molbank;2023-04-17