Molecule

10-Hydroxylyalosidic Acid

AlkaPlorer ID: AK520345

Synonym: None

IUPAC Name: (2S,3R,4S)-3-ethenyl-4-[(6-hydroxy-9H-pyrido[3,4-b]indol-1-yl)methyl]-2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylic acid

Structure

SMILES: C=C[C@H]1[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)OC=C(C(=O)O)[C@H]1CC1=NC=CC2=C1NC1=CC=C(O)C=C12

InChI: InChI=1S/C26H28N2O10/c1-2-12-14(8-18-20-13(5-6-27-18)15-7-11(30)3-4-17(15)28-20)16(24(34)35)10-36-25(12)38-26-23(33)22(32)21(31)19(9-29)37-26/h2-7,10,12,14,19,21-23,25-26,28-33H,1,8-9H2,(H,34,35)/t12-,14+,19-,21-,22+,23-,25+,26-/m1/s1

InChIKey: SDJXJLVNEMUOTE-IWJPDFKUSA-N

Reference

Hydrolytic degradation of .BETA.-carboline-type monoterpenoid glucoindole alkaloids : A possible mechanism for harman formation in Ophiorrhiza and related rubiaceous plants.

PubChem CID: 163188336

LOTUS: LTS0054864

Source

Species	Genus	Family	Order	Class	Phylum	Kingdom	Domain
Ophiorrhiza japonica	Ophiorrhiza	Rubiaceae	Gentianales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota

Properties Information

Molecule Weight: 528.5140000000002

TPSA？: 194.82

MolLogP？: 0.5239000000000007

Number of H-Donors: 7

Number of H-Acceptors: 10

RingCount: 5

Activities Information

Organism	Target Name	Standard Type	Standard Value	Standard Units	doi