ajmalicine

group of stereoisomers with the chemical formula C₂₁H₂₄N₂O₃
ChemicalSubstance group_of_stereoisomers Q104167434
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ajmalicine

Summary

ajmalicine is a group of stereoisomers[1].

Key Facts

  • ajmalicine's instance of is recorded as group of stereoisomers[2].
  • ajmalicine's canonical SMILES is recorded as O=C(OC)C1=COC(C)C2CN3CCC=4C=5C=CC=CC5NC4C3CC12[3].
  • ajmalicine's InChI is recorded as InChI=1S/C21H24N2O3/c1-12-16-10-23-8-7-14-13-5-3-4-6-18(13)22-20(14)19(23)9-15(16)17(11-26-12)21(24)25-2/h3-6,11-12,15-16,19,22H,7-10H2,1-2H3[4].
  • ajmalicine's InChIKey is recorded as GRTOGORTSDXSFK-UHFFFAOYSA-N[5].
  • ajmalicine's chemical formula is recorded as C₂₁H₂₄N₂O₃[6].
  • ajmalicine's subclass of is recorded as indolo[2,3-a]quinolizine alkaloid[7].
  • ajmalicine's PubChem CID is recorded as 251561[8].
  • ajmalicine's found in taxon is recorded as Rauvolfia verticillata[9].
  • ajmalicine's found in taxon is recorded as Kopsia arborea[10].
  • ajmalicine's found in taxon is recorded as Uncaria rhynchophylla[11].
  • ajmalicine's found in taxon is recorded as Leuconotis griffithii[12].
  • ajmalicine's found in taxon is recorded as Alstonia mairei[13].
  • ajmalicine's found in taxon is recorded as Mappianthus iodoides[14].
  • ajmalicine's found in taxon is recorded as Rhazya stricta[15].
  • ajmalicine's found in taxon is recorded as Vinca major[16].
  • ajmalicine's found in taxon is recorded as Tabernaemontana siphilitica[17].
  • ajmalicine's found in taxon is recorded as Mitragyna[18].
  • ajmalicine's found in taxon is recorded as Vinca erecta[19].
  • ajmalicine's found in taxon is recorded as Tabernaemontana psorocarpa[20].
  • ajmalicine's found in taxon is recorded as Alstonia yunnanensis[21].
  • ajmalicine's found in taxon is recorded as Alstonia scholaris[22].
  • ajmalicine's found in taxon is recorded as Rauwolfia sellowii[23].
  • ajmalicine's found in taxon is recorded as Atropa bella-donna[24].
  • ajmalicine's found in taxon is recorded as Catharanthus roseus[25].
  • ajmalicine's Human Metabolome Database ID is recorded as HMDB0248072[26].

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] . Tryptophan decarboxylase plays an important role in ajmalicine biosynthesis in Rauvolfia verticillata. wikidata.org.
  9. [10] . Biologically active indole alkaloids from Kopsia arborea. wikidata.org.
  10. [11] . Determinação por RMN das configurações relativas e conformações de alcalóides oxindólicos isolados de Uncaria guianensis. wikidata.org.
  11. [12] . Rhazinilam-Leuconolam-Leuconoxine Alkaloids from Leuconotis griffithii. wikidata.org.
  12. [13] . Biologically active vallesamine, strychnan, and rhazinilam alkaloids from Alstonia: Pneumatophorine, a nor-secovallesamine with unusual incorporation of a 3-ethylpyridine moiety. wikidata.org.
  13. [14] . Mappianines A-E, structurally diverse monoterpenoid indole alkaloids from Mappianthus iodoides. wikidata.org.
  14. [15] . Analysis of Indole Alkaloids from Rhazya stricta Hairy Roots by Ultra-Performance Liquid Chromatography-Mass Spectrometry.. wikidata.org.
  15. [16] . The structure of vincanicine. wikidata.org.
  16. [17] . Dippinine C, a New Hexacyclic Chippiine Derivative from a Malayan Tabernaemontana. wikidata.org.
  17. [18] . The Mitragyna Species of Asia. wikidata.org.
  18. [19] . The structure of vincanicine. wikidata.org.
  19. [20] . Dippinine C, a New Hexacyclic Chippiine Derivative from a Malayan Tabernaemontana. wikidata.org.
  20. [21] . Alkaloids from the stem-bark of Alstonia macrophylla. wikidata.org.
  21. [22] . Alkaloids from the stem-bark of Alstonia macrophylla. wikidata.org.
  22. [23] . Communications - Rauwolfia Alkaloids. XXVIII. The Isolation of Raujemidine, An Isomer of Reserpine, from R. canescens. wikidata.org.
  23. [24] . Reinvestigation of the Alkaloid Composition of Atropa belladonna Plants, Root Cultures, and Cell Suspension Cultures. wikidata.org.
  24. [25] . Cytochrome P450 2D6 (CYP2D6) inhibitory constituents of Catharanthus roseus. wikidata.org.
  25. [26] . wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

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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). ajmalicine. Retrieved May 3, 2026, from https://4ort.xyz/entity/ajmalicine
MLA “ajmalicine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/ajmalicine.
BibTeX @misc{4ortxyz_ajmalicine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{ajmalicine}}, year = {2026}, url = {https://4ort.xyz/entity/ajmalicine}, note = {Accessed: 2026-05-03}}
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