Molecule

methyl 1-(1-b-Glucopyranosyl)-1H-indole-3-acetate

AlkaPlorer ID: AK009546

Synonym: 'methyl 1-(1-b-Glucopyranosyl)-1H-indole-3-acetate'

IUPAC Name: methyl 2-[1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]indol-3-yl]acetate

Structure

SMILES: COC(=O)CC1=CN([C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C2=CC=CC=C12

InChI: InChI=1S/C17H21NO7/c1-24-13(20)6-9-7-18(11-5-3-2-4-10(9)11)17-16(23)15(22)14(21)12(8-19)25-17/h2-5,7,12,14-17,19,21-23H,6,8H2,1H3/t12-,14-,15+,16-,17-/m1/s1

InChIKey: UCJQLVSIHYDTNQ-USACIQFYSA-N

Reference

Isolation, Structure Determination, and Sensory Activity of Mouth-Drying and Astringent Nitrogen-Containing Phytochemicals Isolated from Red Currants (<i>Ribes rubrum</i>)

PubChem CID: 16108210

LOTUS: LTS0019398

SuperNatural Ⅲ: SN0366655-02

Source

Species	Genus	Family	Order	Class	Phylum	Kingdom	Domain
Ribes rubrum	Ribes	Grossulariaceae	Saxifragales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota

Properties Information

Molecule Weight: 351.3550000000001

TPSA？: 121.38

MolLogP？: -0.6707999999999996

Number of H-Donors: 4

Number of H-Acceptors: 8

RingCount: 3

Activities Information

Organism	Target Name	Standard Type	Standard Value	Standard Units	doi