karanjin

chemical compound
ChemicalSubstance type_of_chemical_entity Q6368495
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karanjin

Summary

karanjin is a type of chemical entity[1]. karanjin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (4 views/month).[2]

Key Facts

  • karanjin's instance of is recorded as type of chemical entity[3].
  • karanjin's chemical structure is recorded as Karanjin.svg[4].
  • karanjin's CAS Registry Number is recorded as 521-88-0[5].
  • karanjin's EC number is recorded as 208-319-9[6].
  • karanjin's canonical SMILES is recorded as COC1=C(OC2=C(C1=O)C=CC3=C2C=CO3)C4=CC=CC=C4[7].
  • karanjin's InChI is recorded as InChI=1S/C18H12O4/c1-20-18-15(19)13-7-8-14-12(9-10-21-14)17(13)22-16(18)11-5-3-2-4-6-11/h2-10H,1H3[8].
  • karanjin's InChIKey is recorded as LKPQNZRGGNOPPU-UHFFFAOYSA-N[9].
  • karanjin's chemical formula is recorded as C₁₈H₁₂O₄[10].
  • karanjin's subclass of is recorded as 8C-substituted flavone[11].
  • karanjin's ChEMBL ID is recorded as CHEMBL208484[12].
  • karanjin's Freebase ID is recorded as /m/0gpc7n[13].
  • karanjin's UNII is recorded as WV7IM0I02M[14].
  • karanjin's ChemSpider ID is recorded as 90925[15].
  • karanjin's PubChem CID is recorded as 100633[16].
  • karanjin's ChEBI ID is recorded as 166631[17].
  • karanjin's found in taxon is recorded as Fordia cauliflora[18].
  • karanjin's found in taxon is recorded as Dahlstedtia pentaphylla[19].
  • karanjin's found in taxon is recorded as Lonchocarpus heptaphyllus[20].
  • karanjin's found in taxon is recorded as Millettia leucantha[21].
  • karanjin's found in taxon is recorded as Millettia pulchra[22].
  • karanjin's found in taxon is recorded as Tephrosia purpurea[23].
  • karanjin's found in taxon is recorded as Muellera campestris[24].
  • karanjin's found in taxon is recorded as Pongamia glabra[25].
  • karanjin's found in taxon is recorded as Pongamia pinnata[26].
  • karanjin's found in taxon is recorded as Millettia pinnata[27].

Why It Matters

karanjin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (4 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] . Global Substance Registration System. 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] . ChEMBL. Retrieved . wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . Global Substance Registration System. Retrieved . wikidata.org.
  13. [15] . Q2311683. Retrieved . wikidata.org.
  14. [16] . PubChem. Retrieved . wikidata.org.
  15. [17] . ChEBI release 2021-03-01. wikidata.org.
  16. [18] . Two new chalcones from Fordia cauliflora. wikidata.org.
  17. [19] . Prenylated flavonoids as evolutionary indicators in the genus Dahlstedtia. wikidata.org.
  18. [20] . Flavonoids from Lonchocarpus latifolius roots. wikidata.org.
  19. [21] . Studies on the chemical constituents of stem bark of Millettia leucantha: isolation of new chalcones with cytotoxic, anti-herpes simplex virus and anti-inflammatory activities. wikidata.org.
  20. [22] . Chemopreventive flavonoids from Millettia pulchra Kurz var-laxior (Dunn) Z.Wei (Yulangsan) function as Michael reaction acceptors. wikidata.org.
  21. [23] . Prenylated flavonoids from Tephrosia purpurea seeds. wikidata.org.
  22. [24] . Antimycobacterial flavonoids from Derris indica. wikidata.org.
  23. [25] . Glabrachromene-II, A Minor Constituent of Seeds of Pongamia glabra. wikidata.org.
  24. [26] . Studies on the chemical constituents of stem bark of Millettia leucantha: isolation of new chalcones with cytotoxic, anti-herpes simplex virus and anti-inflammatory activities. wikidata.org.
  25. [27] . Studies on the chemical constituents of stem bark of Millettia leucantha: isolation of new chalcones with cytotoxic, anti-herpes simplex virus and anti-inflammatory activities. 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). karanjin. Retrieved May 3, 2026, from https://4ort.xyz/entity/karanjin
MLA “karanjin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/karanjin.
BibTeX @misc{4ortxyz_karanjin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{karanjin}}, year = {2026}, url = {https://4ort.xyz/entity/karanjin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): karanjin — https://4ort.xyz/entity/karanjin (retrieved 2026-05-03)

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