Compounds
ID | Spectrum Quality | Annotated Name |
---|
COMPOUND NPA017701
PROPERTIES
NPAID | NPA017701 |
---|---|
CLUSTER ID | 1386 |
NODE ID | 1164 |
NAME | Termitomycesphin E |
FORMULA | C41H79NO10 |
MOLECULAR WEIGHT (Da) | 746.0800 |
ACCURATE MASS (Da) | 745.5704 |
ORIGIN ORGANISM TYPE | Fungus |
ORIGIN GENUS | Termitomyces |
ORIGIN SPECIES | albuminosus |
InChIKey | XDZZMBPLVSZPPN-KQYYMOEVSA-N |
InChI | InChI=1S/C41H79NO10/c1-4-6-8-10-12-13-14-15-16-18-20-22-28-35(46)40(50)42-32(30-51-41-39(49)38(48)37(47)36(29-43)52-41)34(45)27-24-23-26-33(44)31(3)25-21-19-17-11-9-7-5-2/h24,27,31-39,41,43-49H,4-23,25-26,28-30H2,1-3H3,(H,42,50)/b27-24+/t31?,32-,33?,34+,35+,36+,37+,38-,39+,41+/m0/s1 |
SMILES | CCCCCCCCCCCCCC[C@H](C(=O)N[C@@H](CO[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O)O)O)[C@@H](/C=C/CCC(C(C)CCCCCCCCC)O)O)O |
ORIGINAL ISOLATION REFERENCE
CITATION | Qi, J; Ojika, M; Sakagami, Y Neuritogenic cerebrosides from an edible Chinese mushroom. Part 2: Structures of two additional termitomycesphins and activity enhancement of an inactive cerebroside by hydroxylation Bioorganic and Medicinal Chemistry 2001 9 (8) 2171-2177. | ||
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DOI | 10.1016/s0968-0896(01)00125-0 | PMID | 11504654 |