medicarpin

group of stereosiomers
ChemicalSubstance group_of_stereoisomers Q6806652
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medicarpin

Summary

medicarpin is a group of stereoisomers[1]. medicarpin draws 8 Wikipedia views per month (group_of_stereoisomers category, ranking #211 of 1,063).[2]

Key Facts

  • medicarpin's instance of is recorded as group of stereoisomers[3].
  • medicarpin's CAS Registry Number is recorded as 33983-40-3[4].
  • medicarpin's canonical SMILES is recorded as CCOC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)O[5].
  • medicarpin's InChI is recorded as InChI=1S/C16H14O4/c1-18-10-3-5-11-13-8-19-14-6-9(17)2-4-12(14)16(13)20-15(11)7-10/h2-7,13,16-17H,8H2,1H3[6].
  • medicarpin's InChIKey is recorded as NSRJSISNDPOJOP-UHFFFAOYSA-N[7].
  • medicarpin's chemical formula is recorded as C₁₆H₁₄O₄[8].
  • medicarpin's subclass of is recorded as isoflavane[9].
  • medicarpin's part of is recorded as pterocarpan synthase activity[10].
  • medicarpin's ChEMBL ID is recorded as CHEMBL238823[11].
  • medicarpin's Freebase ID is recorded as /m/0gg5gqv[12].
  • medicarpin's PubChem CID is recorded as 623060[13].
  • medicarpin's ChEBI ID is recorded as 16114[14].
  • medicarpin's found in taxon is recorded as Butea superba[15].
  • medicarpin's found in taxon is recorded as Canavalia galeata[16].
  • medicarpin's found in taxon is recorded as Trifolium pratense[17].
  • medicarpin's found in taxon is recorded as Canavalia bonariensis[18].
  • medicarpin's found in taxon is recorded as Canavalia gladiata[19].
  • medicarpin's found in taxon is recorded as Canavalia sericea[20].
  • medicarpin's found in taxon is recorded as Canavalia eurycarpa[21].
  • medicarpin's found in taxon is recorded as Canavalia cathartica[22].
  • medicarpin's found in taxon is recorded as Dalbergia assamica[23].
  • medicarpin's found in taxon is recorded as Canavalia rosea[24].
  • medicarpin's found in taxon is recorded as Tephrosia villosa[25].
  • medicarpin's found in taxon is recorded as Gliricidia[26].
  • medicarpin's found in taxon is recorded as Cicer arietinum[27].

Why It Matters

medicarpin draws 8 Wikipedia views per month (group_of_stereoisomers category, ranking #211 of 1,063).[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] . wikidata.org.
  4. [6] . PubChem. wikidata.org.
  5. [7] . PubChem. wikidata.org.
  6. [8] . PubChem. wikidata.org.
  7. [9] . wikidata.org.
  8. [10] . geneontology.org. Retrieved . geneontology.org. Provenance: wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . Isolation of New Isoflavonolignans, Butesuperins A and B, from a Thai Miracle Herb, Butea superba. wikidata.org.
  14. [16] . Demethylhomopterocarpin: An antifungal compound in Canavalia ensiformis and Vigna unguiculata following infection. wikidata.org.
  15. [17] . Notizen: Isoflavonoid Phytoalexins from Leaves of Trifolium arvense. wikidata.org.
  16. [18] . Demethylhomopterocarpin: An antifungal compound in Canavalia ensiformis and Vigna unguiculata following infection. wikidata.org.
  17. [19] . Demethylhomopterocarpin: An antifungal compound in Canavalia ensiformis and Vigna unguiculata following infection. wikidata.org.
  18. [20] . Demethylhomopterocarpin: An antifungal compound in Canavalia ensiformis and Vigna unguiculata following infection. wikidata.org.
  19. [21] . Demethylhomopterocarpin: An antifungal compound in Canavalia ensiformis and Vigna unguiculata following infection. wikidata.org.
  20. [22] . Demethylhomopterocarpin: An antifungal compound in Canavalia ensiformis and Vigna unguiculata following infection. wikidata.org.
  21. [23] . Isoflavonoid Phytoalexins from Leaflets of Dalbergia sericea. wikidata.org.
  22. [24] . Demethylhomopterocarpin: An antifungal compound in Canavalia ensiformis and Vigna unguiculata following infection. wikidata.org.
  23. [25] . Activity-Guided Isolation of Constituents of Tephrosia purpurea with the Potential to Induce the Phase II Enzyme, Quinone Reductase. wikidata.org.
  24. [26] . Isoflavonoids and a pterocarpan from Gliricidia sepium. wikidata.org.
  25. [27] . Isolation and identification of Cicer isoflavonoids. 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). medicarpin. Retrieved May 3, 2026, from https://4ort.xyz/entity/medicarpin
MLA “medicarpin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/medicarpin.
BibTeX @misc{4ortxyz_medicarpin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{medicarpin}}, year = {2026}, url = {https://4ort.xyz/entity/medicarpin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): medicarpin — https://4ort.xyz/entity/medicarpin (retrieved 2026-05-03)

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