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coniferin

chemical compound
ChemicalSubstance type_of_chemical_entity Q358968
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coniferin

Summary

coniferin is a type of chemical entity[1]. coniferin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (10 views/month).[2]

Key Facts

  • coniferin's instance of is recorded as type of chemical entity[3].
  • coniferin's chemical structure is recorded as Coniferin structure.svg[4].
  • coniferin's CAS Registry Number is recorded as 531-29-3[5].
  • coniferin's EC number is recorded as 803-885-9[6].
  • coniferin's canonical SMILES is recorded as COC1=C(C=CC(=C1)C=CCO)OC2C(C(C(C(O2)CO)O)O)O[7].
  • coniferin's InChI is recorded as InChI=1S/C16H22O8/c1-22-11-7-9(3-2-6-17)4-5-10(11)23-16-15(21)14(20)13(19)12(8-18)24-16/h2-5,7,12-21H,6,8H2,1H3/b3-2+/t12-,13-,14+,15-,16-/m1/s1[8].
  • coniferin's InChIKey is recorded as SFLMUHDGSQZDOW-FAOXUISGSA-N[9].
  • coniferin's chemical formula is recorded as C₁₆H₂₂O₈[10].
  • coniferin's subclass of is recorded as Laricin[11].
  • coniferin's part of is recorded as coniferin metabolic process[12].
  • coniferin's part of is recorded as coniferyl-alcohol glucosyltransferase activity[13].
  • coniferin's part of is recorded as coniferin beta-glucosidase activity[14].
  • coniferin's ChEMBL ID is recorded as CHEMBL459056[15].
  • coniferin's Freebase ID is recorded as /m/03nnljd[16].
  • coniferin's UNII is recorded as M6616XLU2J[17].
  • coniferin's ChemSpider ID is recorded as 4444067[18].
  • coniferin's PubChem CID is recorded as 5280372[19].
  • coniferin's KEGG ID is recorded as C00761[20].
  • coniferin's ChEBI ID is recorded as 16220[21].
  • coniferin's found in taxon is recorded as Mutisia acerosa[22].
  • coniferin's found in taxon is recorded as Picea abies[23].
  • coniferin's found in taxon is recorded as Cynomorium songaricum[24].
  • coniferin's found in taxon is recorded as Balanophora abbreviata[25].
  • coniferin's found in taxon is recorded as Rhodiola crenulata[26].
  • coniferin's found in taxon is recorded as Stachys byzantina[27].

Why It Matters

coniferin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (10 views/month).[2] coniferin has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[28] coniferin is known by 7 alternative names across languages and contexts.[29]

References

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

Direct Wikidata claims

  1. [3] ↑ . wikidata.org.
  2. [4] ↑ . wikidata.org.
  3. [5] ↑ . ChEBI. Retrieved . wikidata.org.
  4. [6] ↑ . ECHA Substance Infocard database. Retrieved . wikidata.org.
  5. [7] ↑ . PubChem. Retrieved . wikidata.org.
  6. [8] ↑ . PubChem. Retrieved . wikidata.org.
  7. [9] ↑ . PubChem. Retrieved . wikidata.org.
  8. [10] ↑ . PubChem. Retrieved . wikidata.org.
  9. [11] ↑ . wikidata.org.
  10. [12] ↑ . Gene Ontology release 2020-05-02. wikidata.org.
  11. [13] ↑ . Gene Ontology release 2020-05-02. wikidata.org.
  12. [14] ↑ . Gene Ontology release 2020-05-02. wikidata.org.
  13. [15] ↑ . ChEMBL. Retrieved . wikidata.org.
  14. [16] ↑ . Freebase Data Dumps. wikidata.org.
  15. [17] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  16. [18] ↑ . Q2311683. Retrieved . wikidata.org.
  17. [19] ↑ . PubChem. Retrieved . wikidata.org.
  18. [20] ↑ . wikidata.org.
  19. [21] ↑ . ChEBI. Retrieved . wikidata.org.
  20. [22] ↑ . Sesquiterpenes and other constituents from chilean mutisieae. wikidata.org.
  21. [23] ↑ . Characterisation of Phenolic Constituents from Juvenile and Mature Needles of Norway Spruce by Means of High Performance Liquid Chromatography-Mass Spectrometry. wikidata.org.
  22. [24] ↑ . Inhibitory effects of ursolic acid derivatives from Cynomorium songaricum, and related triterpenes on human immunodeficiency viral protease. wikidata.org.
  23. [25] ↑ . A New Lignan (I) from Balanophora abbreviata and Inhibition of Lipopolysaccharide (LPS)-Induced Inducible Nitric Oxide Synthase (iNOS) Expression.. wikidata.org.
  24. [26] ↑ . Bioactive constituents from Chinese natural medicines. XXVIII. Chemical structures of acyclic alcohol glycosides from the roots of Rhodiola crenulata. wikidata.org.
  25. [27] ↑ . Iridoid glycoside constituents of Stachys lanata. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] ↑ . Wikidata sitelinks. wikidata.org.
  3. [29] ↑ . Wikidata aliases. 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). coniferin. Retrieved May 3, 2026, from https://4ort.xyz/entity/coniferin
MLA “coniferin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/coniferin.
BibTeX @misc{4ortxyz_coniferin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{coniferin}}, year = {2026}, url = {https://4ort.xyz/entity/coniferin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): coniferin — https://4ort.xyz/entity/coniferin (retrieved 2026-05-03)

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