Home › Entities › (1R,9S,17S)-7,13-diazatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadecan-6-one › (+)-matrine

(+)-matrine

chemical compound
Class type of: (1R,9S,17S)-7,13-diazatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadecan-6-one Q6787831

Facts

10 properties
Instance of
type of chemical entity
Subclass of
(1R,9S,17S)-7,13-diazatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadecan-6-one
Canonical SMILES
C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1
Chemical formula
C₁₅H₂₄N₂O
Found in taxon
Sophora microphylla, Daphniphyllum oldhamii, Daphniphyllum pentandrum, Euchresta formosana, Cuscuta chilensis, Leontice leontopetalum, Sophora chrysophylla, Sophora macrocarpa, Sophora pachycarpa, Sophora tetraptera, Sophora tomentosa, Gymnospermium alberti, Megaselia flavescens, Sophora lehmannii, Sophora flavescens, Sophora alopecuroides, Sophora tonkinensis, Sophora jaubertii, Styphnolobium japonicum, Sophora lehmanni, Sophora davidii
Has characteristic
bitterness
Isomeric SMILES
O=C1CCC[C@@H]2[C@H]3CCCN4CCC[C@@H](CN12)[C@@H]34
Mass
+248.188863388
Physically interacts with
taste receptor type 2
Stereoisomer of
(1S,2R,9R,17S)-7,13-diazatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadecan-6-one, (+)-isomatrine, (−)-sophoridine, (−)-allomatrine, (−)-matrine, (+)-sophoridine, (+)-allomatrine
🏷️ Also known as
en (7aS,13aR,13bR,13cS)-dodecahydro-1H,5H,10H-dipyrido[2,1-f:3′,2′,1′-ij][1,6]naphthyridin-10-one en (+)-matrine en matrine de (+)-Matrin es Matrina ja マトリン pl (+)-matryna zh 苦参碱

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🔗 Connections
Found in taxon 19
Styphnolobium japonicum, Sophora tomentosa, Sophora alopecuroides, Sophora flavescens, Sophora chrysophylla, Sophora pachycarpa, Sophora tetraptera, Sophora davidii +11 more
Has characteristic 1
bitterness
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Summary

(+)-matrine is a type of chemical entity[1]. (+)-matrine is a type of (1R,9S,17S)-7,13-diazatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadecan-6-one[2].

Key Facts

  • Physically interacts with: taste receptor type 2[3]
  • Canonical SMILES: C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1[4]
  • Chemical formula: C₁₅H₂₄N₂O[5]
  • Found in taxon: Sophora microphylla[6], Daphniphyllum oldhamii[7], Daphniphyllum pentandrum[8], Euchresta formosana[9], Cuscuta chilensis[10], Leontice leontopetalum[11], Sophora chrysophylla[12], Sophora macrocarpa[13], Sophora pachycarpa[14], Sophora tetraptera[15], Sophora tomentosa[16], Gymnospermium alberti[17], Megaselia flavescens[18], Sophora lehmannii[19]
  • Has characteristic: bitterness[20]
  • Isomeric SMILES: O=C1CCC[C@@H]2[C@H]3CCCN4CCCC@@H[C@@H]34C@@H[C@@H]34">[21]
  • Mass: 248.188863388 dalton[22]
  • Stereoisomer of: (1S,2R,9R,17S)-7,13-diazatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadecan-6-one[23], (+)-isomatrine[24], (−)-sophoridine[25], (−)-allomatrine[26], (−)-matrine[27], (+)-sophoridine[28], (+)-allomatrine[29]

References

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

Direct Wikidata claims

  1. [3] ↑ . Bitter substances from plants used in traditional Chinese medicine exert biased activation of human bitter taste receptors. wikidata.org.
  2. [4] ↑ . PubChem. wikidata.org.
  3. [5] ↑ . PubChem. wikidata.org.
  4. [2] ↑ . wikidata.org.
  5. [6] ↑ . Alkaloid-Bearing Plants and Their Contained Alkaloids. 1957-1968. wikidata.org.
  6. [7] ↑ . Alkaloids from Daphniphyllum oldhami. wikidata.org.
  7. [8] ↑ . Alkaloids from Daphniphyllum oldhami. wikidata.org.
  8. [9] ↑ . Cytotoxic coumaronochromones from the roots of Euchresta formosana.. wikidata.org.
  9. [10] ↑ . Flavonoids and alkaloids from Cuscuta (Cuscutaceae). wikidata.org.
  10. [11] ↑ . Distribution and taxonomic significance of quinolizidine alkaloids in Leontice leontopetalum and L. ewersmannii (Berberidacea). wikidata.org.
  11. [12] ↑ . Lupin alkaloids from sophora chrysophylla. wikidata.org.
  12. [13] ↑ . alpha-Matrine from Sophora macrocarpa Sm. wikidata.org.
  13. [14] ↑ . The biosynthesis of the alkaloids of Goebelia pachycarpa. wikidata.org.
  14. [15] ↑ . Alkaloids of sophora tetraptera sensu reiche. wikidata.org.
  15. [16] ↑ . Sophora tomentosa Linn.. wikidata.org.
  16. [17] ↑ . A study of the alkaloids ofLeontice albertii. wikidata.org.
  17. [18] ↑ . (+)-12alpha-Hydroxysophocarpine, a new quinolizidine alkaloid and related anti-HBV alkaloids from Sophora flavescens. wikidata.org.
  18. [19] ↑ . An investigation of the alkaloids of Ammothamnus lehmanni the structure of lehmannine. wikidata.org.
  19. [20] ↑ . BitterDB. wikidata.org.
  20. [21] ↑ . wikidata.org.
  21. [22] ↑ . wikidata.org.
  22. [23] ↑ . wikidata.org.
  23. [24] ↑ . wikidata.org.
  24. [25] ↑ . wikidata.org.
  25. [26] ↑ . wikidata.org.
  26. [27] ↑ . wikidata.org.
  27. [28] ↑ . wikidata.org.
  28. [29] ↑ . 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). (+)-matrine. Retrieved November 2, 2026, from https://4ort.xyz/entity/matrine
MLA “(+)-matrine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 2 Nov. 2026, https://4ort.xyz/entity/matrine.
BibTeX @misc{4ortxyz_matrine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{(+)-matrine}}, year = {2026}, url = {https://4ort.xyz/entity/matrine}, note = {Accessed: 2026-11-02}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): (+)-matrine — https://4ort.xyz/entity/matrine (retrieved 2026-11-02)

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Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 19w ago · Nabbegat · 2026-06-19 view diff on Wikidata ↗
    Stereoisomer of → (1S,2R,9R,17S)-7,13-diazatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadecan-6-one, (+)-isomatrine, (−)-sophoridine +4
    Instance of → type of chemical entity
    Has characteristic → bitterness
    Subclass of → —
    + 6 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update-languages-short:0||tr */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/37300|batch #37300]]"
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