Your browser doesn't support javascript.
loading
Paranazzamides A and B, new cyclic dipeptides containing a C7-prenylated tryptophan, produced by pathogenic reptile fungi Paranannizziopsis sp. UH-21.
Kobayashi, Keisuke; Tejima, Rio; Nagai, Kenichiro; Seki, Reiko; Hosoya, Tsuyoshi; Une, Yumi; Shigeno, Satoru; Tomoda, Hiroshi; Ohshiro, Taichi.
Afiliação
  • Kobayashi K; Department of Microbial Chemistry, Graduate School of Pharmaceutical Sciences, Kitasato University, 5-9-1 Shirokane, Minato-ku, Tokyo, 108-8641, Japan.
  • Tejima R; Medicinal Research Laboratories, School of Pharmacy, Kitasato University, 5-9-1 Shirokane, Minato-ku, Tokyo, 108-8641, Japan.
  • Nagai K; Department of Microbial Chemistry, Graduate School of Pharmaceutical Sciences, Kitasato University, 5-9-1 Shirokane, Minato-ku, Tokyo, 108-8641, Japan.
  • Seki R; Medicinal Research Laboratories, School of Pharmacy, Kitasato University, 5-9-1 Shirokane, Minato-ku, Tokyo, 108-8641, Japan.
  • Hosoya T; Medicinal Research Laboratories, School of Pharmacy, Kitasato University, 5-9-1 Shirokane, Minato-ku, Tokyo, 108-8641, Japan.
  • Une Y; Department of Botany, National Museum of Nature and Science, 4-4-1 Amakubo, Tsukuba, Ibaraki, 305-0005, Japan.
  • Shigeno S; Laboratory of Veterinary Pathology, Okayama University of Science, 1-3 Ikoinooka, Imabari, Ehime, Japan.
  • Tomoda H; Department of Microbial Chemistry, Graduate School of Pharmaceutical Sciences, Kitasato University, 5-9-1 Shirokane, Minato-ku, Tokyo, 108-8641, Japan.
  • Ohshiro T; Medicinal Research Laboratories, School of Pharmacy, Kitasato University, 5-9-1 Shirokane, Minato-ku, Tokyo, 108-8641, Japan.
J Antibiot (Tokyo) ; 77(7): 403-411, 2024 Jul.
Article em En | MEDLINE | ID: mdl-38750250
ABSTRACT
Two new cyclic dipeptides, paranazzamides A (1) and B (2) containing a C7-prenylated tryptophan, were isolated from a culture broth of snake fungal disease-isolate Paranannizziopsis sp. UH-21. This is the first report on the new secondary metabolites from Paranannizziopsis sp. The planar structures of 1 and 2 were elucidated using various spectroscopic techniques including MS and 1D/2D NMR. The absolute configuration of 1 was assigned by comparison with the synthesized compound. Compounds 1 and 2 exhibited no antifungal activity, no antibacterial activity, and no cytotoxic activity even at a concentration of 128 µg ml-1, whereas 1 and 2 exhibited amphotericin B potentiating activity against Candida auris in combination treatment.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Peptídeos Cíclicos / Triptofano / Dipeptídeos Limite: Animals / Humans Idioma: En Revista: J Antibiot (Tokyo) Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Peptídeos Cíclicos / Triptofano / Dipeptídeos Limite: Animals / Humans Idioma: En Revista: J Antibiot (Tokyo) Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Japão