Structure Database (LMSD)

OH H O H O H OH OH HO HO O HO O
Common Name
Pfaffiaglycoside B
Systematic Name
3-O-β-D-glucuronoyl-3β,16β-dihydroxyolean-12,20(30)-dien-28-oic acid
Synonyms
LM ID
LMPR0106150062
Formula
Exact Mass
Calculate m/z
632.35605
Status
Active

Main

Classification

String Representations

InChiKey (Click to copy)
FLWTUJKVYNTUKI-KCEJQVNSSA-N
InChi (Click to copy)
InChI=1S/C35H52O10/c1-17-9-14-35(30(42)43)19(15-17)18-7-8-21-32(4)12-11-23(44-29-26(39)24(37)25(38)27(45-29)28(40)41)31(2,3)20(32)10-13-33(21,5)34(18,6)16-22(35)36/h7,19-27,29,36-39H,1,8-16H2,2-6H3,(H,40,41)(H,42,43)/t19-,20-,21+,22-,23-,24-,25-,26+,27-,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)=O)[C@@H](O)C[C@@]4(C)[C@]3(C)CC[C@@]2([H])C(C)(C)[C@H]1O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](C(=O)O)O1

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

Other Databases

PubChem CID

Calculated Physicochemical Properties

Heavy Atoms 45
Rings 6
Aromatic Rings
Rotatable Bonds 4
Van der Waals Molecular Volume 617.24
Topological Polar Surface Area 176.05
Hydrogen Bond Donors 6
Hydrogen Bond Acceptors 10
logP 5.66
Molar Refractivity 166.20

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Created at
9th Jan 2024
Updated at
9th Jan 2024