(Q5526833)

(2R,3R,4S,5R,6S)-2-(hydroxymethyl)-6-[4-(hydroxymethyl)phenoxy]oxane-3,4,5-triol

Gastrodin (English)

8 October 2016

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

(2R,3R,4R,5R,6S)-2-(hydroxymethyl)-6-[4-(hydroxymethyl)phenoxy]oxane-3,4,5-triol

1 reference

based on heuristic

inferred from InChI

chemical formula

C₁₃H₁₈O₇

1 reference

Gastrodin (English)

20 November 2016

C1=CC(=CC=C1CO)OC2C(C(C(C(O2)CO)O)O)O

1 reference

Gastrodin (English)

20 November 2016

C1=CC(=CC=C1CO)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O

1 reference

Phenolic and furan type compounds isolated from Gastrodia elata and their anti-platelet effects

Gastrodin (English)

20 November 2016

13 references

DEVELOPMENT OF HPLC METHOD FOR THE DETERMINATION OF GASTRODIN AND PARA-HYDROXYBENZYL ALCOHOL IN TALL GASTRODIA TUBER ON THE POLYGLYCOL-C8COLUMN

IDENTIFICATION AND DETERMINATION OF THE ACTIVE COMPOUNDS IN GASTRODIA ELATA BLUME BY HPLC

Determination and pharmacokinetics of gastrodin and p-hydroxybenzylalcohol after oral administration of Gastrodia elata Bl. extract in rats by high-performance liquid chromatography-electrospray ionization mass spectrometric method

Isolation and identification of succinic semialdehyde dehydrogenase inhibitory compound from the rhizome of Gastrodia elata Blume

Identification and determination of active components in Gastrodia elata Bl. by capillary electrophoresis

Determination of the active ingredients in Gastrodia rhizoma by capillary electrophoresis with electrochemical detection

Effects of Gastrodia elata and its active constituents on scopolamine-induced amnesia in rats

Simultaneous determination of p-hydroxybenzaldehyde, p-hydroxybenzyl alcohol, 4-(beta-D-glucopyranosyloxy)-benzyl alcohol, and sugars in Gastrodia elata blume measured as their acetylated derivatives by GC-MS.

Neuroprotective Principles fromGastrodiaelata

Two new benzofurans from Gastrodia elata and their DNA topoisomerases I and II inhibitory activities

Studies on the constituents of Gastrodia elata Blume.

Effects of Gastrodia elata and its active constituents on scopolamine-induced amnesia in rats

Cremastra appendiculata

1 reference

Chemical constituents from tubers of Cremastra appendiculata

Gymnadenia conopsea

2 references

Glycosidic constituents of the tubers of Gymnadenia conopsea

Bioactive constituents from Chinese natural medicines. XVII. constituents with radical scavenging effect and new glucosyloxybenzyl 2-isobutylmalates from Gymnadenia conopsea

Anoectochilus formosanus

2 references

Glycosidic constituents from in vitro Anoectochilus formosanus

Glycosidic constituents from in vitro Anoectochilus formosanus

Anoectochilus koshunensis

2 references

Aliphatic and aromatic glucosides from Anoectochilus koshunensis

Aliphatic and aromatic glucosides from Anoectochilus koshunensis

Galeola faberi

2 references

New Phenolic Derivatives from Galeola faberi

New Phenolic Derivatives from Galeola faberi

Cyrtosia septentrionalis

1 reference

[Studies on Galeola septentrionalis Reichb. fil. I. Isolation and structures of the constituents of "Dotuusoo"]

Bletilla formosana

1 reference

Dihydrophenanthrenes from Bletilla formosana

Citrullus colocynthis

1 reference

Bioactive saponins and glycosides. XXVII. Structures of new cucurbitane-type triterpene glycosides and antiallergic constituents from Citrullus colocynthis

Pyrus bourgaeana

1 reference

New benzyl alcohol glycosides from Pyrus bourgaeana

Pyrus communis

1 reference

New benzyl alcohol glycosides from Pyrus bourgaeana

Sicana odorifera

1 reference

Free and bound volatile composition and characterization of some glucoconjugates as aroma precursors in melón de olor fruit pulp (Sicana odorifera).

Dactylorhiza hatagirea

1 reference

Studies on Nepalese Crude Drugs. XXVI. Chemical Constituents of Panch Aunle, the Roots of Dactylorhiza hatagirea D. DON.

Orchidaceae

1 reference

[Studies on Galeola septentrionalis Reichb. fil. I. Isolation and structures of the constituents of "Dotuusoo"]

Identifiers

InChI

InChI=1S/C13H18O7/c14-5-7-1-3-8(4-2-7)19-13-12(18)11(17)10(16)9(6-15)20-13/h1-4,9-18H,5-6H2/t9-,10-,11+,12-,13-/m1/s1

1 reference

Gastrodin (English)

20 November 2016

2 references

Gastrodin (English)

20 November 2016

ChEBI release 2020-09-01

CAS Registry Number

62499-27-8

2 references

Global Substance Registration System

UNII

5YS9U2W3RQ

gastrodin (English)

20 November 2016

https://commonchemistry.cas.org/detail?cas_rn=62499-27-8

9 April 2021

1 reference

beta-Gastrodin (English)

20 November 2016

2 references

Gastrodin (English)

20 November 2016

InChIKey

ChEBI ID

80828

mapping relation type

2 references

GASTRODIN (English)

20 November 2016

International Chemical Identifier

InChI

InChI=1S/C13H18O7/c14-5-7-1-3-8(4-2-7)19-13-12(18)11(17)10(16)9(6-15)20-13/h1-4,9-18H,5-6H2/t9-,10-,11+,12-,13-/m1/s1

1 reference

splash10-0kmr-1962000000-1338a6c32128070f60db

GASTRODIN (English)

20 November 2016

1 reference

0 references

DSSTox substance ID

DTXSID30978086

1 reference

InChIKey

DSSTOX compound identifier

DTXCID301405414

0 references

EC number

683-202-7

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.208.712

27 December 2018

ECHA Substance Infocard ID

[No public or meaningful name is available] (English)

quotation

CAS no.: 62499-27-8 (English)

100.208.712

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.208.712

27 December 2018

[No public or meaningful name is available] (English)

quotation

CAS no.: 62499-27-8 (English)

UNII

5YS9U2W3RQ

2 references

Global Substance Registration System

UNII

5YS9U2W3RQ

gastrodin (English)

20 November 2016

InChIKey

PatientsLikeMe treatment ID

0 references

0 references

1 reference