Conoflorine

chemical compound
ChemicalSubstance group_of_stereoisomers Q83034242
Press Enter · cited answer in seconds

Conoflorine

Summary

Conoflorine is a group of stereoisomers[1].

Key Facts

  • Conoflorine's instance of is recorded as group of stereoisomers[2].
  • Conoflorine's CAS Registry Number is recorded as 15266-46-3[3].
  • Conoflorine's canonical SMILES is recorded as O1C2CN3CCC=4C=5C=CC=CC5NC4CCC(C3)(CC)C12[4].
  • Conoflorine's InChI is recorded as InChI=1S/C19H24N2O/c1-2-19-9-7-16-14(13-5-3-4-6-15(13)20-16)8-10-21(12-19)11-17-18(19)22-17/h3-6,17-18,20H,2,7-12H2,1H3/t17-,18-,19-/m1/s1[5].
  • Conoflorine's InChIKey is recorded as OGDFTQDRHAGLTB-GUDVDZBRSA-N[6].
  • Conoflorine's chemical formula is recorded as C₁₉H₂₄N₂O[7].
  • Conoflorine's subclass of is recorded as alkaloid[8].
  • Conoflorine's PubChem CID is recorded as 453208[9].
  • Conoflorine's found in taxon is recorded as Tabernanthe iboga[10].
  • Conoflorine's found in taxon is recorded as Tabernaemontana grandiflora[11].
  • Conoflorine's found in taxon is recorded as Trachelospermum jasminoides[12].
  • Conoflorine's found in taxon is recorded as Tabernaemontana divaricata[13].
  • Conoflorine's isomeric SMILES is recorded as CC[C@]12CCc3[nH]c4ccccc4c3CCN(C[C@H]3O[C@H]31)C2[14].
  • Conoflorine's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+296.188863388'}[15].
  • Conoflorine's SureChEMBL ID is recorded as 30045921[16].
  • Conoflorine's DSSTox substance ID is recorded as DTXSID10165093[17].
  • Conoflorine's DSSTOX compound identifier is recorded as DTXCID9087584[18].
  • Conoflorine's UniChem compound ID is recorded as 351973[19].

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] . wikidata.org.
  4. [5] . wikidata.org.
  5. [6] . wikidata.org.
  6. [7] . wikidata.org.
  7. [8] . wikidata.org.
  8. [9] . PubChem. Retrieved . wikidata.org.
  9. [10] . Indole alkaloids from cell suspension cultures of Tabernaemontana divaricata and Tabernanthe iboga. wikidata.org.
  10. [11] . Alkaloids of Stemmadenia grandiflora. wikidata.org.
  11. [12] . Indole Alkaloids from Trachelospermum jasminoides. wikidata.org.
  12. [13] . Indole alkaloids from cell suspension cultures of Tabernaemontana divaricata and Tabernanthe iboga. wikidata.org.
  13. [14] . wikidata.org.
  14. [15] . wikidata.org.
  15. [16] . wikidata.org.
  16. [17] . wikidata.org.
  17. [18] . wikidata.org.
  18. [19] . 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). Conoflorine. Retrieved May 3, 2026, from https://4ort.xyz/entity/conoflorine
MLA “Conoflorine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/conoflorine.
BibTeX @misc{4ortxyz_conoflorine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Conoflorine}}, year = {2026}, url = {https://4ort.xyz/entity/conoflorine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Conoflorine — https://4ort.xyz/entity/conoflorine (retrieved 2026-05-03)

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