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Isochromophilones H-K, the new bioactive azaphilone derivatives isolated from fungal strain Diaporthe perseae associated with Pongamia pinnata plant.
Niaz, Shah Iram; Akram, Muhammad; Ullah, Mohib; Safdar, Kamran; Amin, Adnan; Badshah, Syed; Ali, Muhammad; Alsaiari, Ahad Amer; Rehman, Khalil Ur; Khan, Dilfaraz.
Afiliação
  • Niaz SI; Institute of Chemical Sciences, Gomal University, D.I. Khan 29111, KPK, Pakistan.
  • Akram M; PCSIR Labs Complex, Peshawar, KPK, Pakistan.
  • Ullah M; Department of Chemistry, University of Gwadar, Gwadar-91200, Balochistan, Pakistan.
  • Safdar K; Institute of Chemical Sciences, Gomal University, D.I. Khan 29111, KPK, Pakistan.
  • Amin A; Department of Pharmacognosy, Faculty of Pharmacy, Gomal University, D.I. Khan 29111, KPK, Pakistan.
  • Badshah S; Institute of Chemical Sciences, Gomal University, D.I. Khan 29111, KPK, Pakistan.
  • Ali M; Department of Marine Biotechnology, National Sun Yat-sen University, Kaohsiung, B0424, Taiwan.
  • Alsaiari AA; Department of Clinical Laboratory Science, College of Applied Medical Science, Taif University, Taif, Saudi Arabia.
  • Rehman KU; Institute of Chemical Sciences, Gomal University, D.I. Khan 29111, KPK, Pakistan. Electronic address: rehmankhalil025@gmail.com.
  • Khan D; Institute of Chemical Sciences, Gomal University, D.I. Khan 29111, KPK, Pakistan. Electronic address: dilfarazkhan@gu.edu.pk.
Microb Pathog ; 196: 106976, 2024 Sep 21.
Article em En | MEDLINE | ID: mdl-39313134
ABSTRACT
The phytochemical study of the Diaporthe species has revealed significant classes of mycotoxins and phomopsins. Dihydroanthracenone derivatives, chromanones and isochromophilones have also been isolated from Diaporthe sp. These findings led us to explore the Diaporthe perseae for phytochemical analysis that resulted in the isolation of four new compounds designated as isochromophilones H-K (1-4), alongside three previously identified metabolites. Using extensive spectroscopic investigations such as NMR, and Mass spectroscopy, their structures were elucidated. Furthermore, the antimicrobial and anti-diabetic potentials of all isolated compounds were assessed. Compounds 1-3 demonstrated significant antibacterial activity, while compounds 4-7 exhibited comparatively lower effectiveness than the reference antibiotics. Compounds 2-3 showed potent diabetic inhibition, displaying IC50 values of 16.3 ± 0.3 and 25.4 ± 0.3, respectively. Compounds 1, 5, and 6 displayed mild anti-diabetic effects, with IC50 values of 56.5 ± 0.8, 37.6 ± 0.4, and 48.2 ± 0.6. However, compounds 4 and 7 were found least active.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article