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Details

Stereochemistry ABSOLUTE
Molecular Formula C13H18O7
Molecular Weight 286.2778
Optical Activity UNSPECIFIED
Defined Stereocenters 5 / 5
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GASTRODIN

SMILES

OC[C@H]1O[C@@H](OC2=CC=C(CO)C=C2)[C@H](O)[C@@H](O)[C@@H]1O

InChI

InChIKey=PUQSUZTXKPLAPR-UJPOAAIJSA-N
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

HIDE SMILES / InChI

Description
Curator's Comment: Description was created based on several sources, including

Gastrodin is the main bioactive component of Gastrodia elata Blume (G. elata). Tian Ma Su Zhu She Ye (contains Gastrodin) It is an extensively used in the clinical practice of traditional Chinese medicine, to treat neurasthenia, neurasthenia syndrome, angioneurotic headache disorder, traumatic brain syndrome, vertigo meniere disease, medicinal with dizziness, vertigo, sudden deafness, vestibular neuronitis, vertebral basilar artery blood supply deficiency, etc. Apart from traditional claims, scientific reports support the antioxidative, anticonvulsive, antiinflammatory, antiepileptic, antiobesity, anxiolytic, and learning and memory improvements in activities of gastrodin

CNS Activity

Curator's Comment: Gastrodin is CNS active in animals. Gastrodin is the main bioactive component of Gastrodia elata Blume (G. elata). It is an extensively used in the clinical practice of traditional Chinese medicine, to treat headache, migraine, dizziness, epilepsy, infantile convulsion, tetany and so on.

Originator

Sources: Chow J, Yang YB, Yang TR A new phenolic glucoside of Gastrodia elata Blume - gastrodin. Kexue Tongbao. 1979. 24:335-336
Curator's Comment: reference retrieved from https://books.google.ru/books?id=xmHwCAAAQBAJ&dq

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
1.94 µM [Kd]
Conditions
PubMed

PubMed

TitleDatePubMed
Effects of Gastrodia elata and its active constituents on scopolamine-induced amnesia in rats.
1996 Aug
Gastrodin and p-hydroxybenzyl alcohol facilitate memory consolidation and retrieval, but not acquisition, on the passive avoidance task in rats.
1997 Mar
[The production of gastrodin through biotransformation of p-hydroxybenzaldehyde by cell suspension culture of Datura stramonium].
2006 Oct
Pharmacologically active compounds in the Anoectochilus and Goodyera species.
2008 Apr
Gastrodin stimulates anticancer immune response and represses transplanted H22 hepatic ascitic tumor cell growth: Involvement of NF-κB signaling activation in CD4+ T cells.
2013 Jun 15
Patents

Sample Use Guides

Gastrodin injection (unspecified dosage) is beneficial to old patients with refractory hypertension. Gastrodin (50 - 100 mg/kg, intraperitoneally) can decrease the volume of cerebral infarction, ameliorate the cerebral injury in the rats of cerebral ischemia-reperfusion.
Route of Administration: Parenteral
Gastrodin could effectively promote proliferation of rat RSC96 Schwann cells in a dose- and time-dependent manner. The best performance was obtained at the concentration of 200μM.
Name Type Language
GASTRODIN
INCI   MI   WHO-DD  
INCI  
Official Name English
(-)-GASTRODIN
Common Name English
4-HYDROXYBENZYL ALCOHOL 4-O-.BETA.-D-GLUCOPYRANOSIDE
Common Name English
GASTRODIN [MI]
Common Name English
4-(.BETA.-D-GLUCOPYRANOSYLOXY)BENZYL ALCOHOL
Common Name English
.BETA.-D-GLUCOPYRANOSIDE, 4-(HYDROXYMETHYL)PHENYL
Common Name English
Gastrodin [WHO-DD]
Common Name English
4-(.BETA.-D-GLUCOPYRANOSYL)-BENZYLALCOHOL
Common Name English
.BETA.-D-GLUCOPYRANOSIDE, 4-(HYDROXYMETHYL)PHENYL-
Common Name English
GASTRODIN [INCI]
Common Name English
Code System Code Type Description
FDA UNII
5YS9U2W3RQ
Created by admin on Fri Dec 15 15:31:19 GMT 2023 , Edited by admin on Fri Dec 15 15:31:19 GMT 2023
PRIMARY
PUBCHEM
115067
Created by admin on Fri Dec 15 15:31:19 GMT 2023 , Edited by admin on Fri Dec 15 15:31:19 GMT 2023
PRIMARY
WIKIPEDIA
Gastrodin
Created by admin on Fri Dec 15 15:31:19 GMT 2023 , Edited by admin on Fri Dec 15 15:31:19 GMT 2023
PRIMARY
EPA CompTox
DTXSID30978086
Created by admin on Fri Dec 15 15:31:19 GMT 2023 , Edited by admin on Fri Dec 15 15:31:19 GMT 2023
PRIMARY
SMS_ID
100000167075
Created by admin on Fri Dec 15 15:31:19 GMT 2023 , Edited by admin on Fri Dec 15 15:31:19 GMT 2023
PRIMARY
EVMPD
SUB181409
Created by admin on Fri Dec 15 15:31:19 GMT 2023 , Edited by admin on Fri Dec 15 15:31:19 GMT 2023
PRIMARY
MERCK INDEX
m5678
Created by admin on Fri Dec 15 15:31:19 GMT 2023 , Edited by admin on Fri Dec 15 15:31:19 GMT 2023
PRIMARY Merck Index
CAS
62499-27-8
Created by admin on Fri Dec 15 15:31:19 GMT 2023 , Edited by admin on Fri Dec 15 15:31:19 GMT 2023
PRIMARY