LIPID MAPS

Structure Database (LMSD)

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Common Name

Pfaffiaglycoside A

Systematic Name

3β,16β-dihydroxyolean-12,20(30)-dien-28-oyl-β-D-glucopyranose

Synonyms

LM ID

LMPR0106150061

Formula

C₃₅H₅₄O₉

Exact Mass

Calculate m/z

618.376785

Status

Active

Show lipids differing only in stereochemistry/bond geometry

Main

Classification

String Representations

InChiKey (Click to copy)

DTTMCCVFOHHSSH-QDAMGARXSA-N

InChi (Click to copy)

InChI=1S/C35H54O9/c1-18-9-14-35(30(42)44-29-28(41)27(40)26(39)21(17-36)43-29)20(15-18)19-7-8-23-32(4)12-11-24(37)31(2,3)22(32)10-13-33(23,5)34(19,6)16-25(35)38/h7,20-29,36-41H,1,8-17H2,2-6H3/t20-,21+,22-,23+,24-,25-,26+,27-,28+,29-,32-,33+,34+,35+/m0/s1

SMILES (Click to copy)

C1C[C@]2(C)[C@@]3([H])CC=C4[C@]5([H])CC(=C)CC[C@]5(C(O[C@H]5[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O5)=O)[C@@H](O)C[C@@]4(C)[C@]3(C)CC[C@@]2([H])C(C)(C)[C@H]1O

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