gastrodin

chemical compound

Facts

8 properties
Instance of
type of chemical entity
Canonical SMILES
C1=CC(=CC=C1CO)OC2C(C(C(C(O2)CO)O)O)O
Chemical formula
C₁₃H₁₈O₇
Isomeric SMILES
C1=CC(=CC=C1CO)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O
Mass
+286.105253
Stereoisomer of
(2R,3R,4S,5R,6S)-2-(hydroxymethyl)-6-[4-(hydroxymethyl)phenoxy]oxane-3,4,5-triol, (2R,3R,4R,5R,6S)-2-(hydroxymethyl)-6-[4-(hydroxymethyl)phenoxy]oxane-3,4,5-triol
🏷️ Also known as
en 4-(Hydroxymethyl)phenyl-beta-D-glucopyranoside en gastrodin es Gastrodina fa گاسترودین ja ガストロジン ko 가스트로딘 zh 天麻甙
🔖 Identifiers · 22
OpenAlex ID
C2781248740
CAS Registry Number
62499-27-8
ChEBI ID
80828
ChEMBL ID
CHEMBL274739
ChemSpider ID
102977
CosIng number
87059
DSSTOX compound identifier
DTXCID301405414
DSSTox substance ID
DTXSID30978086
EC number
683-202-7
ECHA Substance Infocard ID
100.208.712
Freebase ID
/m/0fqs9m1
Show all 22 identifiers +10
KEGG ID
C16964
Microsoft Academic ID (discontinued)
2781248740
PatientsLikeMe treatment ID
gastrodin
Probes And Drugs ID
PD021642
PubChem CID
115067
SureChEMBL ID
1076037
UniChem compound ID
524046

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Summary

gastrodin is a type of chemical entity[1]. gastrodin is a type of 2-(Hydroxymethyl)-6-[4-(hydroxymethyl)phenoxy]oxane-3,4,5-triol[2].

Key Facts

  • Canonical SMILES: C1=CC(=CC=C1CO)OC2C(C(C(C(O2)CO)O)O)O[3]
  • Chemical formula: C₁₃H₁₈O₇[4]
  • Found in taxon: Gastrodia elata[5], Cremastra appendiculata[6], Gymnadenia conopsea[7], Anoectochilus formosanus[8], Anoectochilus koshunensis[9], Galeola faberi[10], Cyrtosia septentrionalis[11], Bletilla formosana[12], Citrullus colocynthis[13], Pyrus bourgaeana[14], Pyrus communis[15], Sicana odorifera[16], Dactylorhiza hatagirea[17], Galeola septentrionalis[18]
  • Isomeric SMILES: C1=CC(=CC=C1CO)O[C@H]2C@@HOC@@HO">[19]
  • Mass: 286.105253 dalton[20]
  • Stereoisomer of: (2R,3R,4S,5R,6S)-2-(hydroxymethyl)-6-[4-(hydroxymethyl)phenoxy]oxane-3,4,5-triol[21], (2R,3R,4R,5R,6S)-2-(hydroxymethyl)-6-[4-(hydroxymethyl)phenoxy]oxane-3,4,5-triol[22]

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [3] ↑ . PubChem. Retrieved . wikidata.org.
  2. [4] ↑ . PubChem. Retrieved . wikidata.org.
  3. [2] ↑ . wikidata.org.
  4. [5] ↑ . Phenolic and furan type compounds isolated from Gastrodia elata and their anti-platelet effects. wikidata.org.
  5. [6] ↑ . Chemical constituents from tubers of Cremastra appendiculata. wikidata.org.
  6. [7] ↑ . Glycosidic constituents of the tubers of Gymnadenia conopsea. wikidata.org.
  7. [8] ↑ . Glycosidic constituents from in vitro Anoectochilus formosanus. wikidata.org.
  8. [9] ↑ . Aliphatic and aromatic glucosides from Anoectochilus koshunensis. wikidata.org.
  9. [10] ↑ . New Phenolic Derivatives from Galeola faberi. wikidata.org.
  10. [11] ↑ . Studies on Galeola septentrionalis Reichb. fil. I. Isolation and structures of the constituents of "Dotuusoo". wikidata.org.
  11. [12] ↑ . Dihydrophenanthrenes from Bletilla formosana. wikidata.org.
  12. [13] ↑ . Bioactive saponins and glycosides. XXVII. Structures of new cucurbitane-type triterpene glycosides and antiallergic constituents from Citrullus colocynthis. wikidata.org.
  13. [14] ↑ . New benzyl alcohol glycosides from Pyrus bourgaeana. wikidata.org.
  14. [15] ↑ . New benzyl alcohol glycosides from Pyrus bourgaeana. wikidata.org.
  15. [16] ↑ . Free and bound volatile composition and characterization of some glucoconjugates as aroma precursors in melón de olor fruit pulp (Sicana odorifera).. wikidata.org.
  16. [17] ↑ . Studies on Nepalese Crude Drugs. XXVI. Chemical Constituents of Panch Aunle, the Roots of Dactylorhiza hatagirea D. DON.. wikidata.org.
  17. [18] ↑ . Studies on Galeola septentrionalis Reichb. fil. I. Isolation and structures of the constituents of "Dotuusoo". wikidata.org.
  18. [19] ↑ . PubChem. Retrieved . wikidata.org.
  19. [20] ↑ . PubChem. Retrieved . wikidata.org.
  20. [21] ↑ . wikidata.org.
  21. [22] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

📑 Cite this page

Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). gastrodin. Retrieved November 11, 2026, from https://4ort.xyz/entity/gastrodin
MLA “gastrodin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 11 Nov. 2026, https://4ort.xyz/entity/gastrodin.
BibTeX @misc{4ortxyz_gastrodin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{gastrodin}}, year = {2026}, url = {https://4ort.xyz/entity/gastrodin}, note = {Accessed: 2026-11-11}}
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Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 27w ago · KaleemBot bot · 2026-05-02 view diff on Wikidata ↗
    Subclass of → 2-(Hydroxymethyl)-6-[4-(hydroxymethyl)phenoxy]oxane-3,4,5-tr
    Stereoisomer of → (2R,3R,4S,5R,6S)-2-(hydroxymethyl)-6-[4-(hydroxymethyl)pheno, (2R,3R,4R,5R,6S)-2-(hydroxymethyl)-6-[4-(hydroxymethyl)pheno
    Mass → 286.105253 dalton
    Instance of → type of chemical entity
    + 1 other property edited (see Wikidata diff for full list)
    "Changed the item: Added ur:گیسٹروڈن"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.