isovitexin

chemical compound
ChemicalSubstance type_of_chemical_entity Q3155636
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isovitexin

Summary

isovitexin is a type of chemical entity[1]. isovitexin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (16 views/month).[2]

Key Facts

  • isovitexin's instance of is recorded as type of chemical entity[3].
  • isovitexin's CAS Registry Number is recorded as 38953-85-4[4].
  • isovitexin's EC number is recorded as 609-600-2[5].
  • isovitexin's canonical SMILES is recorded as C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C=C3O2)O)C4C(C(C(C(O4)CO)O)O)O)O)O[6].
  • isovitexin's InChI is recorded as InChI=1S/C21H20O10/c22-7-14-17(26)19(28)20(29)21(31-14)16-11(25)6-13-15(18(16)27)10(24)5-12(30-13)8-1-3-9(23)4-2-8/h1-6,14,17,19-23,25-29H,7H2/t14-,17-,19+,20-,21+/m1/s1[7].
  • isovitexin's InChIKey is recorded as MYXNWGACZJSMBT-VJXVFPJBSA-N[8].
  • isovitexin's chemical formula is recorded as C₂₁H₂₀O₁₀[9].
  • isovitexin's subclass of is recorded as 6C-glycosylated flavone[10].
  • isovitexin's ChEMBL ID is recorded as CHEMBL465360[11].
  • isovitexin's Freebase ID is recorded as /m/0n508h9[12].
  • isovitexin's UNII is recorded as KTQ9R9MS0Q[13].
  • isovitexin's ChemSpider ID is recorded as 142556[14].
  • isovitexin's PubChem CID is recorded as 162350[15].
  • isovitexin's KEGG ID is recorded as C01714[16].
  • isovitexin's ChEBI ID is recorded as 18330[17].
  • isovitexin's found in taxon is recorded as Epidendrum rigidum[18].
  • isovitexin's found in taxon is recorded as Ocimum gratissimum[19].
  • isovitexin's found in taxon is recorded as Passiflora incarnata[20].
  • isovitexin's found in taxon is recorded as Cerastium arvense[21].
  • isovitexin's found in taxon is recorded as Combretum micranthum[22].
  • isovitexin's found in taxon is recorded as Oenothera brachycarpa[23].
  • isovitexin's found in taxon is recorded as Oenothera macrocarpa[24].
  • isovitexin's found in taxon is recorded as Crataegus oxyacantha L. (1753)[25].
  • isovitexin's found in taxon is recorded as Passiflora alata[26].
  • isovitexin's found in taxon is recorded as Carex fraseriana[27].

Why It Matters

isovitexin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (16 views/month).[2] isovitexin has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[28]

References

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

Direct Wikidata claims

  1. [3] . wikidata.org.
  2. [4] . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  3. [5] . ECHA Substance Infocard database. Retrieved . wikidata.org.
  4. [6] . PubChem. Retrieved . wikidata.org.
  5. [7] . PubChem. Retrieved . wikidata.org.
  6. [8] . PubChem. Retrieved . wikidata.org.
  7. [9] . PubChem. Retrieved . wikidata.org.
  8. [10] . wikidata.org.
  9. [11] . ChEMBL. Retrieved . wikidata.org.
  10. [12] . Freebase Data Dumps. wikidata.org.
  11. [13] . Global Substance Registration System. Retrieved . wikidata.org.
  12. [14] . Q2311683. Retrieved . wikidata.org.
  13. [15] . PubChem. Retrieved . wikidata.org.
  14. [16] . wikidata.org.
  15. [17] . ChEBI. Retrieved . wikidata.org.
  16. [18] . Phytotoxic activity of bibenzyl derivatives from the orchid Epidendrum rigidum.. wikidata.org.
  17. [19] . The application of atmospheric pressure chemical ionisation liquid chromatography-mass spectrometry in the chemotaxonomic study of flavonoids: characterisation of flavonoids from Ocimum gratissimum var. gratissimum. wikidata.org.
  18. [20] . Separation of flavone C-glycosides and qualitative analysis of Passiflora incarnata L. by capillary zone electrophoresis. wikidata.org.
  19. [21] . Isomollupentin-O-glucosides from Cerastium arvense. wikidata.org.
  20. [22] . Flavonoids ofEupatorium micranthum. wikidata.org.
  21. [23] . The Flavonoids of Oenothera Sect. Megapterium (Onagraceae). wikidata.org.
  22. [24] . The Flavonoids of Oenothera Sect. Megapterium (Onagraceae). wikidata.org.
  23. [25] . Phenolic Extracts from Meadowsweet and Hawthorn Flowers Have Antioxidative Properties. wikidata.org.
  24. [26] . Pharmacological trials of crude extract of Passiflora alata. wikidata.org.
  25. [27] . Taxonomic implications of the flavonoids of Cymophyllus fraseri (Cyperaceae). 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.

📑 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). isovitexin. Retrieved May 3, 2026, from https://4ort.xyz/entity/isovitexin
MLA “isovitexin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/isovitexin.
BibTeX @misc{4ortxyz_isovitexin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{isovitexin}}, year = {2026}, url = {https://4ort.xyz/entity/isovitexin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): isovitexin — https://4ort.xyz/entity/isovitexin (retrieved 2026-05-03)

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