Home › Entities › group_of_stereoisomers › vinorine

vinorine

chemical compound
ChemicalSubstance group_of_stereoisomers Q15427935
Press Enter · cited answer in seconds

vinorine

Summary

vinorine is a group of stereoisomers[1].

Key Facts

  • vinorine's instance of is recorded as group of stereoisomers[2].
  • vinorine's chemical structure is recorded as Vinorine.svg[3].
  • vinorine's canonical SMILES is recorded as CC=C1CN2C3CC1C4C2CC5(C4OC(=O)C)C3=NC6=CC=CC=C56[4].
  • vinorine's InChI is recorded as InChI=1S/C21H22N2O2/c1-3-12-10-23-16-8-13(12)18-17(23)9-21(20(18)25-11(2)24)14-6-4-5-7-15(14)22-19(16)21/h3-7,13,16-18,20H,8-10H2,1-2H3/b12-3-/t13-,16-,17-,18?,20+,21+/m0/s1[5].
  • vinorine's InChIKey is recorded as CLDVMRAEPFQOSD-WEOXKLFPSA-N[6].
  • vinorine's chemical formula is recorded as C₂₁H₂₂N₂O₂[7].
  • vinorine's subclass of is recorded as chemical compound[8].
  • vinorine's part of is recorded as vinorine hydroxylase activity[9].
  • vinorine's part of is recorded as vinorine synthase activity[10].
  • vinorine's Freebase ID is recorded as /m/0xnh135[11].
  • vinorine's ChemSpider ID is recorded as 4445243[12].
  • vinorine's PubChem CID is recorded as 5281974[13].
  • vinorine's KEGG ID is recorded as C11807[14].
  • vinorine's ChEBI ID is recorded as 16791[15].
  • vinorine's found in taxon is recorded as Vinca minor[16].
  • vinorine's found in taxon is recorded as Rauvolfia serpentina[17].
  • vinorine's isomeric SMILES is recorded as C/C=C\1/CN2[C@H]3C[C@@H]1C4[C@@H]2C[C@]5([C@@H]4OC(=O)C)C3=NC6=CC=CC=C56[18].
  • vinorine's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+334.168128'}[19].
  • vinorine's SureChEMBL ID is recorded as 29741362[20].
  • vinorine's UniChem compound ID is recorded as 1070426[21].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . wikidata.org.
  3. [4] ↑ . PubChem. Retrieved . wikidata.org.
  4. [5] ↑ . PubChem. Retrieved . wikidata.org.
  5. [6] ↑ . PubChem. Retrieved . wikidata.org.
  6. [7] ↑ . PubChem. Retrieved . wikidata.org.
  7. [8] ↑ . wikidata.org.
  8. [9] ↑ . Gene Ontology release 2020-05-02. wikidata.org.
  9. [10] ↑ . Gene Ontology release 2020-05-02. wikidata.org.
  10. [11] ↑ . wikidata.org.
  11. [12] ↑ . Q2311683. Retrieved . wikidata.org.
  12. [13] ↑ . PubChem. Retrieved . wikidata.org.
  13. [14] ↑ . wikidata.org.
  14. [15] ↑ . ChEBI. Retrieved . wikidata.org.
  15. [16] ↑ . Vinca Alkaloids. wikidata.org.
  16. [17] ↑ . Substrate Specificity of Vinorine Hydroxylase, a Novel Membrane-bound Key Enzyme of Rauwolfia Indole Alkaloid Biosynthesis. wikidata.org.
  17. [18] ↑ . PubChem. Retrieved . wikidata.org.
  18. [19] ↑ . PubChem. Retrieved . wikidata.org.
  19. [20] ↑ . wikidata.org.
  20. [21] ↑ . UniChem. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. 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). vinorine. Retrieved May 3, 2026, from https://4ort.xyz/entity/vinorine
MLA “vinorine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/vinorine.
BibTeX @misc{4ortxyz_vinorine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{vinorine}}, year = {2026}, url = {https://4ort.xyz/entity/vinorine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): vinorine — https://4ort.xyz/entity/vinorine (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/vinorine · Last refreshed:

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. 17w ago · Shuaib-bot bot · 2026-05-06 view diff on Wikidata ↗
    Isomeric smiles → C/C=C\1/CN2[C@H]3C[C@@H]1C4[C@@H]2C[C@]5([C@@H]4OC(=O)C)C3=N
    Chebi id → 16791
    Subclass of → chemical compound
    Kegg id → C11807
    + 16 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.