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conquinamine

chemical compound
ChemicalSubstance group_of_stereoisomers Q27256816
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conquinamine

Summary

conquinamine is a group of stereoisomers[1].

Key Facts

  • conquinamine's instance of is recorded as group of stereoisomers[2].
  • conquinamine's CAS Registry Number is recorded as 464-86-8[3].
  • conquinamine's canonical SMILES is recorded as C=CC1CN2CCC1CC2C34C(CCO3)(C5=CC=CC=C5N4)O[4].
  • conquinamine's InChI is recorded as InChI=1S/C19H24N2O2/c1-2-13-12-21-9-7-14(13)11-17(21)19-18(22,8-10-23-19)15-5-3-4-6-16(15)20-19/h2-6,13-14,17,20,22H,1,7-12H2/t13-,14-,17+,18+,19-/m0/s1[5].
  • conquinamine's InChIKey is recorded as ALNKTVLUDWIWIH-JCTKKGROSA-N[6].
  • conquinamine's chemical formula is recorded as C₁₉H₂₄N₂O₂[7].
  • conquinamine's subclass of is recorded as alkaloid[8].
  • conquinamine's ChEMBL ID is recorded as CHEMBL2262629[9].
  • conquinamine's UNII is recorded as 38T72MD4BR[10].
  • conquinamine's ChemSpider ID is recorded as 31148270[11].
  • conquinamine's PubChem CID is recorded as 76319464[12].
  • conquinamine's found in taxon is recorded as Cinchona robusta[13].
  • conquinamine's found in taxon is recorded as Cinchona pubescens[14].
  • conquinamine's found in taxon is recorded as Ciliosemina pedunculata[15].
  • conquinamine's found in taxon is recorded as Cinchona calisaya[16].
  • conquinamine's isomeric SMILES is recorded as C=C[C@H]1CN2CC[C@H]1C[C@@H]2[C@@]34C@@(C5=CC=CC=C5N4)OC@@(C5=CC=CC=C5N4)O">[17].
  • conquinamine's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+312.184'}[18].
  • conquinamine's UniChem compound ID is recorded as 79978540[19].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . Global Substance Registration System. Retrieved . 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] ↑ . ChEMBL. Retrieved . wikidata.org.
  9. [10] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  10. [11] ↑ . Q2311683. Retrieved . wikidata.org.
  11. [12] ↑ . PubChem. Retrieved . wikidata.org.
  12. [13] ↑ . Thermospray Liquid Chromatography/Mass Spectrometry (TSP LC/MS) Analysis of the Alkaloids from Cinchona in vitro Cultures. wikidata.org.
  13. [14] ↑ . Investigation of Cinchona leaf alkaloids by high-performance liquid chromatography. wikidata.org.
  14. [15] ↑ . Five New Alkaloids from the Leaves of Remijia peruviana. wikidata.org.
  15. [16] ↑ . Investigation of Cinchona leaf alkaloids by high-performance liquid chromatography. wikidata.org.
  16. [17] ↑ . PubChem. Retrieved . wikidata.org.
  17. [18] ↑ . PubChem. Retrieved . wikidata.org.
  18. [19] ↑ . UniChem. 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). conquinamine. Retrieved May 3, 2026, from https://4ort.xyz/entity/conquinamine
MLA “conquinamine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/conquinamine.
BibTeX @misc{4ortxyz_conquinamine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{conquinamine}}, year = {2026}, url = {https://4ort.xyz/entity/conquinamine}, note = {Accessed: 2026-05-03}}
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