input word = C00023916

Metabolite InformationStructural formula
Name Hebevinoside I
3beta,16beta-Dihydroxy-7beta-methoxycucurbita-5,24-diene-3-O-beta-D-xylopyranoside-16-O-(6-O-acetyl)-beta-D-glucopyranoside
Formula C44H72O13
Mw 808.49729239
CAS RN 87396-30-3
C_ID C00023916 ,
InChIKey PEVRNEDRRNBORS-ADGDIUHHNA-N
InChICode InChI=1S/C44H72O13/c1-22(2)12-11-13-23(3)32-29(55-40-37(51)35(49)34(48)30(56-40)21-53-24(4)45)19-44(9)38-28(52-10)18-26-25(42(38,7)16-17-43(32,44)8)14-15-31(41(26,5)6)57-39-36(50)33(47)27(46)20-54-39/h12,18,23,25,27-40,46-51H,11,13-17,19-21H2,1-10H3/t23-,25-,27-,28-,29-,30-,31-,32+,33+,34+,35+,36+,37+,38+,39+,40-,42-,43+,44+/m0/s1
SMILES CO[C@H]1C=C2C(CC[C@H](O[C@H]3OC[C@@H](O)[C@@H](O)C3O)C2(C)C)[C@]2(C)CCC3(C)C(C(C)CCC=C(C)C)[C@@H](O[C@H]4OC(COC(C)=O)[C@H](O)C(O)[C@H]4O)CC3(C)C12
Start Substs in Alk. Biosynthesis (Prediction)
Organism
Kingdom Family Species Reference
FungiHymenogastraceaeHebeloma vinosphyllum Ref.
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OrganismHebeloma vinosphyllum
ReferenceFujimoto,Chem.Pharm.Bull.,34,(1986),88-89