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Secondary metabolites isolated from Trichoderma hamatum b-3 and their fungicidal activity.
Huang, Li; Liu, Meng-Dan; Hu, Yi-Wen; Chen, Li-Juan; Deng, Yun; Gu, Yu-Cheng; Bian, Qiang; Guo, Da-Le; Wang, Guang-Zhi.
Afiliación
  • Huang L; State Key Laboratory of Southwestern Chinese Medicine Resource, School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
  • Liu MD; State Key Laboratory of Southwestern Chinese Medicine Resource, School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
  • Hu YW; State Key Laboratory of Southwestern Chinese Medicine Resource, School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
  • Chen LJ; State Key Laboratory of Southwestern Chinese Medicine Resource, School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
  • Deng Y; State Key Laboratory of Southwestern Chinese Medicine Resource, School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
  • Gu YC; Syngenta Jealott's Hill International Research Centre, Berkshire, UK.
  • Bian Q; National Pesticide Engineering Research Center (Tianjin), State Key Laboratory of Elemento-Organic Chemistry, College of Chemistry, Nankai University, Tianjin 300071, China.
  • Guo DL; State Key Laboratory of Southwestern Chinese Medicine Resource, School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu, China. Electronic address: guodale@cdutcm.edu.cn.
  • Wang GZ; State Key Laboratory of Southwestern Chinese Medicine Resource, School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu, China. Electronic address: wangguangzhi@cdutcm.edu.cn.
Fitoterapia ; 174: 105880, 2024 Apr.
Article en En | MEDLINE | ID: mdl-38431026
ABSTRACT
An undescribed trichodenone derivative (1), two new diketopiperazines (3 and 4) along with a bisabolane analog (2) were isolated from Trichoderma hamatum b-3. The structures of the new findings were established through comprehensive analyses of spectral evidences in HRESIMS, 1D and 2D NMR, Marfey's analysis as well as comparisons of ECD. The absolute configuration of 2 was unambiguously confirmed by NMR, ECD calculation and Mo2(AcO)4 induced circular dichroism. Compounds 1-4 were tested for their fungicidal effects against eight crop pathogenic fungi, among which 1 showed 51% inhibition against Sclerotinia sclerotiorum at a concentration of 50 µg/mL.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Trichoderma / Hypocreales Idioma: En Revista: Fitoterapia Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Trichoderma / Hypocreales Idioma: En Revista: Fitoterapia Año: 2024 Tipo del documento: Article País de afiliación: China