Compounds
ID | Spectrum Quality | Annotated Name |
---|
COMPOUND NPA004822
PROPERTIES
NPAID | NPA004822 |
---|---|
CLUSTER ID | 1386 |
NODE ID | 1164 |
NAME | Termitomycesphin F |
FORMULA | C43H83NO10 |
MOLECULAR WEIGHT (Da) | 774.1340 |
ACCURATE MASS (Da) | 773.6017 |
ORIGIN ORGANISM TYPE | Fungus |
ORIGIN GENUS | Termitomyces |
ORIGIN SPECIES | albuminosus |
InChIKey | BJMQARSMRDABQI-LOJLZSRWSA-N |
InChI | InChI=1S/C43H83NO10/c1-4-6-8-10-12-13-14-15-16-17-18-20-22-24-30-37(48)42(52)44-34(32-53-43-41(51)40(50)39(49)38(31-45)54-43)36(47)29-26-25-28-35(46)33(3)27-23-21-19-11-9-7-5-2/h26,29,33-41,43,45-51H,4-25,27-28,30-32H2,1-3H3,(H,44,52)/b29-26+/t33?,34-,35?,36+,37+,38+,39+,40-,41+,43+/m0/s1 |
SMILES | CCCCCCCCCCCCCCCC[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 |