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trans-norbixin

chemical compound
ChemicalSubstance type_of_chemical_entity Q1997371
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trans-norbixin

Summary

trans-norbixin is a type of chemical entity[1]. trans-norbixin is known by 4 alternative names across languages and contexts.[2]

Key Facts

  • trans-norbixin's instance of is recorded as type of chemical entity[3].
  • trans-norbixin's chemical structure is recorded as Norbixin structure.png[4].
  • trans-norbixin's CAS Registry Number is recorded as 542-40-5[5].
  • trans-norbixin's EC number is recorded as 208-810-8[6].
  • trans-norbixin's canonical SMILES is recorded as CC(=CC=CC=C(C)C=CC=C(C)C=CC(=O)O)C=CC=C(C)C=CC(=O)O[7].
  • trans-norbixin's InChI is recorded as InChI=1S/C24H28O4/c1-19(11-7-13-21(3)15-17-23(25)26)9-5-6-10-20(2)12-8-14-22(4)16-18-24(27)28/h5-18H,1-4H3,(H,25,26)(H,27,28)/b6-5+,11-7+,12-8+,17-15+,18-16+,19-9+,20-10+,21-13+,22-14+[8].
  • trans-norbixin's InChIKey is recorded as ZVKOASAVGLETCT-UOGKPENDSA-N[9].
  • trans-norbixin's chemical formula is recorded as C₂₄H₂₈O₄[10].
  • trans-norbixin's subclass of is recorded as fatty acid[11].
  • trans-norbixin's subclass of is recorded as apocarotenoid[12].
  • trans-norbixin's Commons category is recorded as Norbixin[13].
  • trans-norbixin's ChEMBL ID is recorded as CHEMBL1602127[14].
  • trans-norbixin's UNII is recorded as E8M59E17AI[15].
  • trans-norbixin's ChemSpider ID is recorded as 4444661[16].
  • trans-norbixin's PubChem CID is recorded as 5281249[17].
  • trans-norbixin's KEGG ID is recorded as C08608[18].
  • trans-norbixin's ChEBI ID is recorded as 7623[19].
  • trans-norbixin's found in taxon is recorded as Bixa orellana[20].
  • trans-norbixin's DrugBank ID is recorded as DB15201[21].
  • trans-norbixin's isomeric SMILES is recorded as C/C(=C\C=C\C=C(\C=C\C=C(\C=C\C(=O)O)/C)/C)/C=C/C=C(/C=C/C(=O)O)\C[22].
  • trans-norbixin's LIPID MAPS ID is recorded as LMPR01070209[23].
  • trans-norbixin's KNApSAcK ID is recorded as C00003782[24].
  • trans-norbixin's mass is recorded as {'unit': 'Q483261', 'amount': '+380.198759'}[25].
  • trans-norbixin's ECHA Substance Infocard ID is recorded as 100.008.010[26].
  • trans-norbixin's Google Knowledge Graph ID is recorded as /g/1215jt62[27].

Why It Matters

trans-norbixin is known by 4 alternative names across languages and contexts.[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] ↑ . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . ChEMBL. Retrieved . wikidata.org.
  13. [15] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  14. [16] ↑ . Q2311683. Retrieved . wikidata.org.
  15. [17] ↑ . PubChem. Retrieved . wikidata.org.
  16. [18] ↑ . ChEBI. Retrieved . wikidata.org.
  17. [19] ↑ . ChEMBL. Retrieved . wikidata.org.
  18. [20] ↑ . A thirteen-week oral toxicity study of annatto extract (norbixin), a natural food color extracted from the seed coat of annatto (Bixa orellana L.), in Sprague-Dawley rats. wikidata.org.
  19. [21] ↑ . wikidata.org.
  20. [22] ↑ . PubChem. Retrieved . wikidata.org.
  21. [23] ↑ . LIPID MAPS. Retrieved . lipidmaps.org. Provenance: wikidata.org.
  22. [24] ↑ . ChEBI. Retrieved . wikidata.org.
  23. [25] ↑ . PubChem. Retrieved . wikidata.org.
  24. [26] ↑ . ECHA Substance Infocard database. Retrieved . wikidata.org.
  25. [27] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . 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). trans-norbixin. Retrieved May 3, 2026, from https://4ort.xyz/entity/trans-norbixin
MLA “trans-norbixin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/trans-norbixin.
BibTeX @misc{4ortxyz_trans-norbixin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{trans-norbixin}}, year = {2026}, url = {https://4ort.xyz/entity/trans-norbixin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): trans-norbixin — https://4ort.xyz/entity/trans-norbixin (retrieved 2026-05-03)

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