Home › Entities › group_of_stereoisomers › Catharanthine hcl

Catharanthine hcl

group of stereoisomers with the chemical formula C₂₁H₂₄N₂O₂
ChemicalSubstance group_of_stereoisomers Q104964772
Press Enter · cited answer in seconds

Catharanthine hcl

Summary

Catharanthine hcl is a group of stereoisomers[1].

Key Facts

  • Catharanthine hcl's instance of is recorded as group of stereoisomers[2].
  • Catharanthine hcl's canonical SMILES is recorded as O=C(OC)C12C=3NC=4C=CC=CC4C3CCN5CC(C=C(CC)C51)C2[3].
  • Catharanthine hcl's InChI is recorded as InChI=1S/C21H24N2O2/c1-3-14-10-13-11-21(20(24)25-2)18-16(8-9-23(12-13)19(14)21)15-6-4-5-7-17(15)22-18/h4-7,10,13,19,22H,3,8-9,11-12H2,1-2H3[4].
  • Catharanthine hcl's InChIKey is recorded as CMKFQVZJOWHHDV-UHFFFAOYSA-N[5].
  • Catharanthine hcl's chemical formula is recorded as C₂₁H₂₄N₂O₂[6].
  • Catharanthine hcl's subclass of is recorded as iboga alkaloid[7].
  • Catharanthine hcl's PubChem CID is recorded as 418553[8].
  • Catharanthine hcl's ChEBI ID is recorded as 182086[9].
  • Catharanthine hcl's found in taxon is recorded as Catharanthus roseus[10].
  • Catharanthine hcl's Human Metabolome Database ID is recorded as HMDB0242242[11].
  • Catharanthine hcl's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+336.183778008'}[12].
  • Catharanthine hcl's SureChEMBL ID is recorded as 835722[13].
  • Catharanthine hcl's MassBank accession ID is recorded as MSBNK-RIKEN-PR310589[14].
  • Catharanthine hcl's NMRShiftDB structure ID is recorded as 10017656[15].
  • Catharanthine hcl's UniChem compound ID is recorded as 23615185[16].
  • Catharanthine hcl's Probes And Drugs ID is recorded as PD056393[17].

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] ↑ . PubChem. Retrieved . wikidata.org.
  8. [9] ↑ . ChEBI release 2022-06-13. wikidata.org.
  9. [10] ↑ . Terpene Moiety Enhancement by Overexpression of Geranyl(geranyl) Diphosphate Synthase and Geraniol Synthase Elevates Monomeric and Dimeric Monoterpene Indole Alkaloids in Transgenic Catharanthus roseus. wikidata.org.
  10. [11] ↑ . wikidata.org.
  11. [12] ↑ . wikidata.org.
  12. [13] ↑ . wikidata.org.
  13. [14] ↑ . MassBank/MassBank-data: release version 2022.06 to wikidata. Retrieved . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . UniChem. wikidata.org.
  16. [17] ↑ . 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). Catharanthine hcl. Retrieved May 3, 2026, from https://4ort.xyz/entity/catharanthine-hcl
MLA “Catharanthine hcl.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/catharanthine-hcl.
BibTeX @misc{4ortxyz_catharanthine-hcl_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Catharanthine hcl}}, year = {2026}, url = {https://4ort.xyz/entity/catharanthine-hcl}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Catharanthine hcl — https://4ort.xyz/entity/catharanthine-hcl (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/catharanthine-hcl · Last refreshed: