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Structure type: monomer ; 491.2988 [M+Na]+
C₂₆H₄₄O₇
Trivial name: hypomonticuside
Compound class: glycoside, diterpene glycoside
Contained glycoepitopes: IEDB_130701,IEDB_144983,IEDB_152206,IEDB_983930,SB_44,SB_67,SB_72

• Article ID: 9189
  Su Y-S, Cheng MJ, Wu MD, Hsieh SY, Chai C-Y, Kwan A-L "New metabolite from the endophytic fungus Corynespora smithii" - Chemistry of Natural Compounds 56 (2020) 452–454
  

  A new isopimarane-type diterpene glycoside, named hypomonticuside (1), was isolated from the BuOH-soluble fraction of the liquid fermentation of an endophytic fungus Corynespora smithii, derived from the stems of Ardisia cornudentata Mez (Myrsinaceae). The structure of 1 was elucidated by spectroscopic methods, including UV, IR, HR-ESI-MS, and extensive 1D and 2D NMR techniques.

  secondary metabolite, diterpene, Xylariaceae, Hypoxylon monticulosum

  Publication DOI: 10.1007/s10600-020-03060-9
  Journal NLM ID: 0047757
  Publisher: New York: Kluwer Academic/Plenum Publishers
  Correspondence: Cheng MJ
  Institutions: Bioresource Collection and Research Center (BCRC), Food Industry Research and Development Institute (FIRDI), Hsinchu, Taiwan, Graduate Institute of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan, Department of Pathology, Kaohsiung Medical University Chung-Ho Memorial Hospital, Kaohsiung, Taiwan, Department of Neurosurgery, Kaohsiung Medical University Chung-Ho Memorial Hospital, Kaohsiung, Taiwan
  Methods: 13C NMR, 1H NMR, EI-MS, NMR-2D, IR, DNA techniques, TLC, UV, extraction, optical rotation measurement, CC, cell growth, HR-ESI-MS, RP-MPLC
  
   
  
  Corynespora smithii
  CSDB ID 50467 (all data & tools)