LIPID MAPS

Structure Database (LMSD)

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Common Name

Kurilensoside H

Systematic Name

(25S)-3β-(β-D-xylopyranosyloxy)-4β,5β-epoxycholestan-6β,8,15α,16β,26-pentol

Synonyms

(25S)-3-O-(beta-D-xylopyranosyl)-4beta,5beta-epoxycholestan-3beta,6beta,8,15alpha,16beta,26-hexol

LM ID

LMST05050017

Formula

C₃₂H₅₄O₁₁

Exact Mass

Calculate m/z

614.366615

Status

Active

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

Hippasteria (#136939)

Asteroidea (#7588)

Steroidal monoglycosides from the Far Eastern starfish Hippasteria kurilensis and hypothetic pathways of polyhydroxysteroid biosynthesis in starfish.,
Steroids, 2009

Pubmed ID: 19059276

String Representations

InChiKey (Click to copy)

SOVMHZODGWLPJC-HMRISKBOSA-N

InChi (Click to copy)

InChI=1S/C32H54O11/c1-15(13-33)6-5-7-16(2)21-23(37)24(38)26-29(21,3)10-9-19-30(4)11-8-18(42-28-25(39)22(36)17(34)14-41-28)27-32(30,43-27)20(35)12-31(19,26)40/h15-28,33-40H,5-14H2,1-4H3/t15-,16+,17+,18-,19+,20+,21-,22-,23+,24-,25+,26+,27-,28-,29+,30+,31-,32-/m0/s1

SMILES (Click to copy)

C1[C@]2(C)[C@@]3([H])CC[C@]4(C)[C@@]([H])([C@]([H])(C)CCC[C@@H](CO)C)[C@@H](O)[C@H](O)[C@@]4([H])[C@]3(O)C[C@@H](O)[C@]32O[C@H]3[C@@H](O[C@@H]2OC[C@@H](O)[C@H](O)[C@H]2O)C1