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(+/-)-dicentrine

chemical compound
ChemicalSubstance group_of_stereoisomers Q27281149
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(+/-)-dicentrine

Summary

(+/-)-dicentrine is a group of stereoisomers[1].

Key Facts

  • (+/-)-dicentrine's instance of is recorded as group of stereoisomers[2].
  • (+/-)-dicentrine's CAS Registry Number is recorded as 26110-43-0[3].
  • (+/-)-dicentrine's canonical SMILES is recorded as CN1CCC2=CC3=C(C4=C2C1CC5=CC(=C(C=C54)OC)OC)OCO3[4].
  • (+/-)-dicentrine's InChI is recorded as InChI=1S/C20H21NO4/c1-21-5-4-11-7-17-20(25-10-24-17)19-13-9-16(23-3)15(22-2)8-12(13)6-14(21)18(11)19/h7-9,14H,4-6,10H2,1-3H3[5].
  • (+/-)-dicentrine's InChIKey is recorded as YJWBWQWUHVXPNC-UHFFFAOYSA-N[6].
  • (+/-)-dicentrine's chemical formula is recorded as C₂₀H₂₁NO₄[7].
  • (+/-)-dicentrine's subclass of is recorded as aporphine alkaloids[8].
  • (+/-)-dicentrine's UNII is recorded as J3IJ5DN3JE[9].
  • (+/-)-dicentrine's ChemSpider ID is recorded as 547811[10].
  • (+/-)-dicentrine's PubChem CID is recorded as 630859[11].
  • (+/-)-dicentrine's found in taxon is recorded as Lindera megaphylla[12].
  • (+/-)-dicentrine's found in taxon is recorded as Cassytha[13].
  • (+/-)-dicentrine's found in taxon is recorded as Stephania brachyandra[14].
  • (+/-)-dicentrine's found in taxon is recorded as Stephania tetrandra[15].
  • (+/-)-dicentrine's found in taxon is recorded as Stephania dicentrinifera[16].
  • (+/-)-dicentrine's found in taxon is recorded as Stephania delavayi[17].
  • (+/-)-dicentrine's found in taxon is recorded as Alstonia scholaris[18].
  • (+/-)-dicentrine's found in taxon is recorded as Stephania mashanica[19].
  • (+/-)-dicentrine's found in taxon is recorded as Stephania abyssinica[20].
  • (+/-)-dicentrine's found in taxon is recorded as Stephania epigaea[21].
  • (+/-)-dicentrine's found in taxon is recorded as Stephania kuinanensis[22].
  • (+/-)-dicentrine's found in taxon is recorded as Stephania pierrei[23].
  • (+/-)-dicentrine's found in taxon is recorded as Ocotea velloziana[24].
  • (+/-)-dicentrine's found in taxon is recorded as Ocotea leucoxylon[25].
  • (+/-)-dicentrine's found in taxon is recorded as Stephania zippeliana[26].

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 . commonchemistry.cas.org. Provenance: 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] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  9. [10] ↑ . Q2311683. Retrieved . wikidata.org.
  10. [11] ↑ . PubChem. Retrieved . wikidata.org.
  11. [12] ↑ . Anti-Tumor Effects ofd-Dicentrine from the Root ofLindera megaphylla. wikidata.org.
  12. [13] ↑ . Vasorelaxing alkaloids and flavonoids from Cassytha filiformis. wikidata.org.
  13. [14] ↑ . Cytotoxic and antimalarial alkaloids from the tubers of Stephania pierrei. wikidata.org.
  14. [15] ↑ . Cytotoxic and antimalarial alkaloids from the tubers of Stephania pierrei. wikidata.org.
  15. [16] ↑ . Cytotoxic and antimalarial alkaloids from the tubers of Stephania pierrei. wikidata.org.
  16. [17] ↑ . Cytotoxic and antimalarial alkaloids from the tubers of Stephania pierrei. wikidata.org.
  17. [18] ↑ . Pharmacological evaluation of Alstonia scholaris: Anti-inflammatory and analgesic effects. wikidata.org.
  18. [19] ↑ . Cytotoxic and antimalarial alkaloids from the tubers of Stephania pierrei. wikidata.org.
  19. [20] ↑ . Cytotoxic and antimalarial alkaloids from the tubers of Stephania pierrei. wikidata.org.
  20. [21] ↑ . Cytotoxic and antimalarial alkaloids from the tubers of Stephania pierrei. wikidata.org.
  21. [22] ↑ . Cytotoxic and antimalarial alkaloids from the tubers of Stephania pierrei. wikidata.org.
  22. [23] ↑ . Morphinanes isomères originaux isolés de Stephaniazippeliana. wikidata.org.
  23. [24] ↑ . Isolation and biochemical characterization of a new topoisomerase I inhibitor from Ocotea leucoxylon. wikidata.org.
  24. [25] ↑ . Benzylisoquinoline alkaloids and flavonols from Ocotea vellosiana. wikidata.org.
  25. [26] ↑ . Cytotoxic and antimalarial alkaloids from the tubers of Stephania pierrei. 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). (+/-)-dicentrine. Retrieved May 3, 2026, from https://4ort.xyz/entity/-dicentrine
MLA “(+/-)-dicentrine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/-dicentrine.
BibTeX @misc{4ortxyz_-dicentrine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{(+/-)-dicentrine}}, year = {2026}, url = {https://4ort.xyz/entity/-dicentrine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): (+/-)-dicentrine — https://4ort.xyz/entity/-dicentrine (retrieved 2026-05-03)

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