LIPID MAPS

Structure Database (LMSD)

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Common Name

15alpha-glucosyl-lithocholic Acid

Systematic Name

3α-hydroxy-15α-O-β-D-glucopyranosyloxy-5β-cholan-24-oic acid

Synonyms

LM ID

LMST04010479

Formula

C₃₀H₅₀O₉

Exact Mass

Calculate m/z

554.345486

Sum Composition

ST 24:1;O4;Hex

Status

Curated

Show lipids differing only in stereochemistry/bond geometry

No other lipid differing only in stereochemistry/bond geometry found

Classification

References

Taxonomy Information

Curated from

NCBI taxonomy class

Reference

Aspergillus minisclerotigenes (#656917)

Eurotiomycetes (#147545)

Ten undescribed derivatives of lithocholic acid produced by biotransformation and their anti-neuroinflammatory activity.,
Steroids, 2026

Pubmed ID: 42476486

DOI: 10.1016/j.steroids.2026.109834

String Representations

InChiKey (Click to copy)

PEDYVMBLERMNGN-ZCCBGPKCSA-N

InChi (Click to copy)

InChI=1S/C30H50O9/c1-15(4-7-23(33)34)20-13-21(38-28-27(37)26(36)25(35)22(14-31)39-28)24-18-6-5-16-12-17(32)8-10-29(16,2)19(18)9-11-30(20,24)3/h15-22,24-28,31-32,35-37H,4-14H2,1-3H3,(H,33,34)/t15-,16-,17-,18-,19+,20-,21+,22-,24-,25-,26+,27-,28-,29+,30-/m1/s1

SMILES (Click to copy)

C1[C@]2(C)[C@@]3([H])CC[C@]4([C@@]([C@]3([H])CC[C@]2([H])C[C@H](O)C1)([H])[C@@H](O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1)C[C@]4([H])[C@]([H])(C)CCC(O)=O)C