Show legend Show as text

Structure type: monomer ; 824.6619 [M-H]-
C₄₈H₉₁NO₉
Trivial name: cortenuamide B
Compound class: cerebroside
Contained glycoepitopes: IEDB_137339,IEDB_142488,IEDB_146664,IEDB_983931,SB_192,SB_5

• Article ID: 7851
  Tan JW, Dong ZJ, Liu JK "New cerebrosides from the basidiomycete Cortinarius tenuipes" - Lipids 38(1) (2003) 81-84
  

  Five cerebrosides (1-5), including three new ones named cortenuamide A (1), cortenuamide B (2), and cortenuamide C (3), were isolated from the fruiting bodies of the basidiomycete Cortinarius tenuipes. The structures of those compounds were elucidated as (4E,8E)-N-D-2′-hydroxytetracosanoyl-1-O-β-D-glycopyranosyl-9-methyl-4,8-sphingadienine (1), (4E,8E)-N-D-2′-hydroxytricosanoyl-1-O-β-D-glycopyranosyl-9-methyl-4,8-sphingadienine (2), (4E,8E)-N-D-2′-hydroxydocosanoyl-1-O-β-D-glycopyranosyl-9-methyl-4,8-sphingadienine (3), (4E,8E)-N-D-2′-hydroxyoctadecanoyl-1-O-β-D-glycopyranosyl-9-methyl-4,8-sphingadienine (4), and (4E,8E)-N-D-2′-hydroxypalmitoyl-1-O-β-D-glycopyranosyl-9-methyl-4,8-sphingadienine (5) by spectral and chemical methods.

  cerebrosides, Cortinarius tenuipes, cortenuamides

  NCBI PubMed ID: 12669823
  Publication DOI: 10.1007/s11745-003-1034-8
  Journal NLM ID: 0060450
  Publisher: American Oil Chemists' Society
  Correspondence: Liu JK
  Institutions: Kunming Institute of Botany, The Chinese Academy of Sciences, Kunming, China
  Methods: 13C NMR, 1H NMR, EI-MS, NMR-2D, IR, FAB-MS, GC-MS, TLC, acid hydrolysis, MS, methanolysis, extraction, optical rotation measurement, CC, reversed-phase chromatography, melting point determination
  
   
  
  Cortinarius tenuipes
  CSDB ID 45901 (all data & tools)

Show legend Show as text

Structure type: monomer
Trivial name: cortenuamide B
Compound class: cerebroside
Contained glycoepitopes: IEDB_137339,IEDB_142488,IEDB_146664,IEDB_983931,SB_192,SB_5

• Article ID: 8363
  Liu JK "Secondary metabolites from higher fungi in China and their biological activity" - Drug Discoveries and Therapeutics 1(2) (2007) 94-103
  

  As a part of our search for naturally occurring bioactive metabolites from higher fungi, we investigated the chemical constituents of basidiomycetes and ascomycetes fungi (Albatrellus confluens, Albatrellus dispansus, Boletus edulis, Boletopsis grisea, Bondarzewia berkeleyi, Cortinarius tenuipes, Cortinarius vibratilis, Daldinia concentrica, Engleromyces goetzii, Hydnum repandum, Hebeloma versipelle, Hygrophorus eburnesus, Lactarius deliciosus, Lactarius hatsudake, Lactarius hirtipes, Lactarius mitissimus, Lactarius rufus, Paxillus panuoides, Pulveroboletus ravenelii, Russula cyanoxantha, Russula foetens, Russula lepida, Russula nigricans, Sarcodon laevigatum, Sarcodon scabrosus, Shiraia bambusicola, Thelephora aurantiotincta, Thelephora ganbajun, Tricholomopsis rutilans, Tylopilus virens, Tuber indicum, Xylaria euglossa, etc.), and isolated a number of novel terpenoids, phenolics, and nitrogen-containing compounds. The isolation, structural elucidation, and biologically activity of the new compounds are discussed

  natural products, secondary metabolites, biological activities, higher fungi

  NCBI PubMed ID: 22504394
  Journal NLM ID: 101493809
  Publisher: Tokyo: Shandong University China-Japan Cooperation Center for Drug Discovery & Screen
  Correspondence: Liu JK
  Institutions: State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, China
  
   
  
  Cortinarius tenuipes
  CSDB ID 48162 (all data & tools)