Synthesis of Acetogenin Analogs Comprising Pyrimidine Moieties Linked by Amine Bonds and Their Inhibitory Activity against Human Cancer Cell Lines.


Journal

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

Informations de publication

Date de publication:
2022
Historique:
entrez: 3 11 2022
pubmed: 4 11 2022
medline: 8 11 2022
Statut: ppublish

Résumé

Here, we synthesized three acetogenin analogs containing pyrimidine moieties linked by amine bonds, which represent the skeleton structure of pyrimidifen, a mitochondrial complex I-inhibiting insecticide. Replacing the pyrimidine moiety linked by the amine bond remarkably enhanced growth-inhibitory activity of the analogs against several human cancer cell lines. Moreover, these analogs selectively and potently inhibited the growth of these human cancer cell lines regardless of the pyrimidine substituents. Furthermore, COMPARE analyses suggested that these analogs inhibited cancer growth by inhibiting mitochondrial complex I. Our study provides insights into the design of acetogenin analogs as novel antitumor agents.

Identifiants

pubmed: 36328525
doi: 10.1248/cpb.c22-00574
doi:

Substances chimiques

Acetogenins 0
Amines 0
Antineoplastic Agents 0
Pyrimidines 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

823-826

Auteurs

Hiroyuki Hosomi (H)

Kyoto Pharmaceutical University.

Akinobu Akatsuka (A)

Cancer Chemotherapy Center, Japanese Foundation for Cancer Research.

Shingo Dan (S)

Cancer Chemotherapy Center, Japanese Foundation for Cancer Research.

Hiroki Iwasaki (H)

Kyoto Pharmaceutical University.

Hisanori Nambu (H)

Kyoto Pharmaceutical University.

Naoto Kojima (N)

Kyoto Pharmaceutical University.

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Classifications MeSH