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Secondary Metabolites of Phomopsis sp. XZ‐26, an Endophytic Fungus from Camptotheca acuminate
Author(s) -
Lin Ting,
Lin Xiang,
Lu Chunhua,
Hu Zhiyu,
Huang Wenyu,
Huang Yaojian,
Shen Yuemao
Publication year - 2009
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.200801021
Subject(s) - phomopsis , chemistry , stereochemistry , two dimensional nuclear magnetic resonance spectroscopy , antimicrobial , terpene , fungus , botany , organic chemistry , biology
Eleven new metabolites, including nine lovastatin analogues [oblongolides N–V ( 1 – 2 and 5 – 11 ), which were defined as naphthalene‐type fungal polyketides], one linear furanopolyketide ( 13 ) and a monoterpene named dihydroxysabinane ( 14 ), together with four known compounds including oblongolides B ( 3 ) and C ( 4 ), one linear furanopolyketide ( 12 ) and the sesterterpene terpestacin ( 15 ), were isolated from the endophytic fungal strain Phomopsis sp. XZ‐26 of Camptotheca acuminate . Their structures were elucidated by spectroscopic analyses including HR‐ESI‐MS, 1 H and 13 C NMR, 2D NMR (HMQC, HMBC, 1 H‐ 1 H COSY and NOESY), and X‐ray single‐crystal analysis. The antimicrobial activities of 1 – 5 , 8 , 10 and 13 – 15 were evaluated, but none showed a substantial effect. Additionally, a hypothetical biosynthetic pathway for oblongolides was proposed.(© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)