Structure-Activity Relationship of Anti-malarial Allylpyrocatechol Isolated from Piper betle.


Journal

Chemical & pharmaceutical bulletin
ISSN: 1347-5223
Titre abrégé: Chem Pharm Bull (Tokyo)
Pays: Japan
ID NLM: 0377775

Informations de publication

Date de publication:
2020
Historique:
entrez: 4 8 2020
pubmed: 4 8 2020
medline: 5 2 2021
Statut: ppublish

Résumé

Malaria disease remains a serious worldwide health problem. In South-East Asia, one of the malaria infection "hot-spots," medicinal plants such as Piper betle have traditionally been used for the treatment of malaria, and allylpyrocatechol (1), a constituent of P. betle, has been shown to exhibit anti-malarial activities. In this study, we verified that 1 showed in vivo anti-malarial activity through not only intraperitoneal (i.p.) but also peroral (p.o.) administration. Additionally, some analogs of 1 were synthesized and the structure-activity relationship was analyzed to disclose the crucial sub-structures for the potent activity.

Identifiants

pubmed: 32741921
doi: 10.1248/cpb.c20-00294
doi:

Substances chimiques

Antimalarials 0
Catechols 0
Plant Extracts 0
allylpyrocatechol 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

784-790

Auteurs

Satoru Tamura (S)

School of Pharmacy, Iwate Medical University.
Graduate School of Pharmaceutical Sciences, Osaka University.

Akihito Miyoshi (A)

Graduate School of Pharmaceutical Sciences, Osaka University.

Tomikazu Kawano (T)

School of Pharmacy, Iwate Medical University.

Toshihiro Horii (T)

Research Institute for Microbial Diseases, Osaka University.

Sawako Itagaki (S)

Research Institute for Microbial Diseases, Osaka University.

Nobutoshi Murakami (N)

Graduate School of Pharmaceutical Sciences, Osaka University.

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Classifications MeSH