LIPID MAPS

Structure Database (LMSD)

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Common Name

Pfaffiaglycoside C

Systematic Name

25-O-(β-D-glucopyranosyl)-2β,3β,14α,20R,25-pentahydroxy-5β-cholest-7-en-6-one

Synonyms

Taxisterone-25-glucoside

LM ID

LMST01010610

Formula

C₃₃H₅₄O₁₁

Exact Mass

Calculate m/z

626.366615

Sum Composition

ST 27:2;O6;Hex

Status

Curated

Show lipids differing only in stereochemistry/bond geometry

Classification

References

Taxonomy Information

Curated from

NCBI taxonomy class

Reference

Pfaffia glomerata (#221785)

Magnoliopsida (#3398)

Brazilian natural medicines. IV. New noroleanane-type triterpene and ecdysterone-type sterol glycosides and melanogenesis inhibitors from the roots of Pfaffia glomerata.,
Chem Pharm Bull (Tokyo), 2010

Pubmed ID: 20460798

String Representations

InChiKey (Click to copy)

UEXXIAIQEQISLX-GAOVYPHCSA-N

InChi (Click to copy)

InChI=1S/C33H54O11/c1-29(2,44-28-27(40)26(39)25(38)23(16-34)43-28)9-6-10-32(5,41)24-8-12-33(42)18-13-20(35)19-14-21(36)22(37)15-30(19,3)17(18)7-11-31(24,33)4/h13,17,19,21-28,34,36-42H,6-12,14-16H2,1-5H3/t17-,19-,21+,22-,23+,24-,25+,26-,27+,28-,30+,31+,32-,33+/m0/s1

SMILES (Click to copy)

C12=CC([C@]3([H])C[C@@H](O)[C@@H](O)C[C@]3(C)[C@@]1([H])CC[C@@]1(C)[C@@]2(O)CC[C@]1([H])[C@](O)(C)CCCC(O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1)(C)C)=O