Oblongine

group of stereoisomers with the chemical formula C₁₉H₂₄NO₃⁺
ChemicalSubstance group_of_stereoisomers Q110077209
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Oblongine

Summary

Oblongine is a group of stereoisomers[1].

Key Facts

  • Oblongine's instance of is recorded as group of stereoisomers[2].
  • Oblongine's CAS Registry Number is recorded as 152230-57-4[3].
  • Oblongine's canonical SMILES is recorded as OC1=CC=C(C=C1)CC2C3=C(O)C(OC)=CC=C3CC[N+]2(C)C[4].
  • Oblongine's InChI is recorded as InChI=1S/C19H23NO3/c1-20(2)11-10-14-6-9-17(23-3)19(22)18(14)16(20)12-13-4-7-15(21)8-5-13/h4-9,16H,10-12H2,1-3H3,(H-,21,22)/p+1[5].
  • Oblongine's InChIKey is recorded as POJZOQWVMMYVBU-UHFFFAOYSA-O[6].
  • Oblongine's chemical formula is recorded as C₁₉H₂₄NO₃⁺[7].
  • Oblongine's subclass of is recorded as organic cation[8].
  • Oblongine's PubChem CID is recorded as 157129[9].
  • Oblongine's ChEBI ID is recorded as 175045[10].
  • Oblongine's found in taxon is recorded as Tiliacora funifera[11].
  • Oblongine's found in taxon is recorded as Stephania tetrandra[12].
  • Oblongine's found in taxon is recorded as Stephania cephalantha[13].
  • Oblongine's found in taxon is recorded as Magnolia officinalis[14].
  • Oblongine's found in taxon is recorded as Q481711[15].
  • Oblongine's Human Metabolome Database ID is recorded as HMDB0040697[16].
  • Oblongine's KNApSAcK ID is recorded as C00052460[17].
  • Oblongine's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+314.17507004809'}[18].
  • Oblongine's DSSTox substance ID is recorded as DTXSID001317701[19].
  • Oblongine's UniChem compound ID is recorded as 276220[20].

References

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

Direct Wikidata claims

  1. [2] . wikidata.org.
  2. [3] . Chemical Abstracts Service. Retrieved . 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] . ChEBI release 2022-06-13. wikidata.org.
  10. [11] . Constituents of West African Medicinal Plants XXV. Isolation of Oblongine from Tiliacora dinklagei and the Synthesis of Oblongine and Related Benzylisoquinoline Alkaloids. wikidata.org.
  11. [12] . Quaternary isoquinoline alkaloids from Stephania cepharantha. wikidata.org.
  12. [13] . Four New Bisbenzylisoquinoline Alkaloids from the Root of Stephania Tetrandra (Fen-Fang Ji). wikidata.org.
  13. [14] . Identification of minor lignans, alkaloids, and phenylpropanoid glycosides in Magnolia officinalis by HPLC‒DAD‒QTOF-MS/MS. wikidata.org.
  14. [15] . Rapid identification and comparative analysis of the chemical constituents and metabolites ofPhellodendri amurensiscortex and Zhibai dihuang pill by ultra-performance liquid chromatography with quadrupole TOF-MS. wikidata.org.
  15. [16] . wikidata.org.
  16. [17] . wikidata.org.
  17. [18] . wikidata.org.
  18. [19] . wikidata.org.
  19. [20] . 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). Oblongine. Retrieved May 3, 2026, from https://4ort.xyz/entity/oblongine
MLA “Oblongine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/oblongine.
BibTeX @misc{4ortxyz_oblongine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Oblongine}}, year = {2026}, url = {https://4ort.xyz/entity/oblongine}, note = {Accessed: 2026-05-03}}
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