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phaseolin

chemical compound
ChemicalSubstance type_of_chemical_entity Q7180982
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phaseolin

Summary

phaseolin is a type of chemical entity[1]. phaseolin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (5 views/month).[2]

Key Facts

  • phaseolin's instance of is recorded as type of chemical entity[3].
  • phaseolin's chemical structure is recorded as Phaseolin structure.svg[4].
  • phaseolin's CAS Registry Number is recorded as 13401-40-6[5].
  • phaseolin's canonical SMILES is recorded as CC1(C=CC2=C(O1)C=CC3=C2OC4C3COC5=C4C=CC(=C5)O)C[6].
  • phaseolin's InChI is recorded as InChI=1S/C20H18O4/c1-20(2)8-7-14-16(24-20)6-5-12-15-10-22-17-9-11(21)3-4-13(17)19(15)23-18(12)14/h3-9,15,19,21H,10H2,1-2H3/t15-,19-/m0/s1[7].
  • phaseolin's InChIKey is recorded as LWTDZKXXJRRKDG-KXBFYZLASA-N[8].
  • phaseolin's chemical formula is recorded as C₂₀H₁₈O₄[9].
  • phaseolin's subclass of is recorded as 3'C-prenylisoflavane[10].
  • phaseolin's ChEMBL ID is recorded as CHEMBL448350[11].
  • phaseolin's Freebase ID is recorded as /m/0gg8njq[12].
  • phaseolin's UNII is recorded as 8OHL7771FZ[13].
  • phaseolin's UNII is recorded as I7OEP19ZWL[14].
  • phaseolin's ChemSpider ID is recorded as 82683[15].
  • phaseolin's PubChem CID is recorded as 91572[16].
  • phaseolin's KEGG ID is recorded as C10514[17].
  • phaseolin's found in taxon is recorded as Erythrina abyssinica[18].
  • phaseolin's found in taxon is recorded as Erythrina burttii[19].
  • phaseolin's found in taxon is recorded as Erythrina sigmoidea[20].
  • phaseolin's found in taxon is recorded as Erythrina suberosa[21].
  • phaseolin's found in taxon is recorded as Erythrina variegata[22].
  • phaseolin's found in taxon is recorded as Glycyrrhiza inflata[23].
  • phaseolin's found in taxon is recorded as Erythrina lysistemon[24].
  • phaseolin's found in taxon is recorded as snap bean[25].
  • phaseolin's found in taxon is recorded as Phaseolus vulgaris[26].
  • phaseolin's found in taxon is recorded as Erythrina addisoniae[27].

Why It Matters

phaseolin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (5 views/month).[2]

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] ↑ . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: 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] ↑ . wikidata.org.
  11. [13] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  12. [14] ↑ . wikidata.org.
  13. [15] ↑ . Q2311683. Retrieved . wikidata.org.
  14. [16] ↑ . PubChem. Retrieved . wikidata.org.
  15. [17] ↑ . ChEBI. Retrieved . wikidata.org.
  16. [18] ↑ . Recent Studies on Bioactive Compounds From Plants. wikidata.org.
  17. [19] ↑ . Three isoflav-3-enes and a 2-arylbenzofuran from the root bark of Erythrina burttii. wikidata.org.
  18. [20] ↑ . An isoflavanone and a coumestan from Erythrina sigmoidea. wikidata.org.
  19. [21] ↑ . Erysubins C-F, four isoflavonoids from Erythrina suberosa var. glabrescences. wikidata.org.
  20. [22] ↑ . Four New Isoflavonoids and a New 2-Arylbenzofuran from the Roots of Erythrina variegata. wikidata.org.
  21. [23] ↑ . Isoprenoid-substituted flavonoids from roots of Glycyrrhiza inflata. wikidata.org.
  22. [24] ↑ . Pterocarpans with inhibitory effects on protein tyrosine phosphatase 1B from Erythrina lysistemon Hutch. wikidata.org.
  23. [25] ↑ . Isoflavonoids from Phaseolus coccineus. wikidata.org.
  24. [26] ↑ . Microassay to measure phytoalexin response in protoplasts of bean leaves. wikidata.org.
  25. [27] ↑ . Pterocarpans phaseollin and neorautenol isolated from Erythrina addisoniae induce apoptotic cell death accompanied by inhibition of ERK phosphorylation. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.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). phaseolin. Retrieved May 3, 2026, from https://4ort.xyz/entity/phaseolin
MLA “phaseolin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/phaseolin.
BibTeX @misc{4ortxyz_phaseolin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{phaseolin}}, year = {2026}, url = {https://4ort.xyz/entity/phaseolin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): phaseolin — https://4ort.xyz/entity/phaseolin (retrieved 2026-05-03)

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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. 4w ago · KaleemBot bot · 2026-04-30 view diff on Wikidata ↗
    Subclass of → 3'C-prenylisoflavane
    Found in taxon → Erythrina abyssinica, Erythrina burttii, Erythrina sigmoidea +10
    Mass → {'unit': 'Q483261', 'amount': '+322.121'}
    Stereoisomer of → (2S,11S)-17,17-dimethyl-4,12,18-trioxapentacyclo[11.8.0.02,11.05,10.014,19]henicosa-1(13),5(10),6,8,14(19),15,20-heptaen-7-ol
    + 5 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ Added [[wikipedia:ur:فیزولن (ٹیرو کارپن)]]"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.