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(17R/S)-vomilenine

group of stereoisomers
ChemicalSubstance group_of_stereoisomers Q15427932
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(17R/S)-vomilenine

Summary

(17R/S)-vomilenine is a group of stereoisomers[1].

Key Facts

  • (17R/S)-vomilenine's instance of is recorded as group of stereoisomers[2].
  • (17R/S)-vomilenine's canonical SMILES is recorded as CC=C1C2CC3C4=NC5=CC=CC=C5C46CC(C2C6OC(=O)C)N3C1O[3].
  • (17R/S)-vomilenine's InChI is recorded as InChI=1S/C21H22N2O3/c1-3-11-12-8-15-18-21(13-6-4-5-7-14(13)22-18)9-16(23(15)20(11)25)17(12)19(21)26-10(2)24/h3-7,12,15-17,19-20,25H,8-9H2,1-2H3/b11-3+/t12-,15-,16-,17?,19+,20+,21+/m0/s1[4].
  • (17R/S)-vomilenine's InChIKey is recorded as BERYBAUEDCRDKM-FDHUPVAHSA-N[5].
  • (17R/S)-vomilenine's chemical formula is recorded as C₂₁H₂₂N₂O₃[6].
  • (17R/S)-vomilenine's subclass of is recorded as vomilenine[7].
  • (17R/S)-vomilenine's part of is recorded as raucaffricine beta-glucosidase activity[8].
  • (17R/S)-vomilenine's part of is recorded as vomilenine glucosyltransferase activity[9].
  • (17R/S)-vomilenine's part of is recorded as vinorine hydroxylase activity[10].
  • (17R/S)-vomilenine's part of is recorded as vomilenine reductase activity[11].
  • (17R/S)-vomilenine's ChemSpider ID is recorded as 10128107[12].
  • (17R/S)-vomilenine's PubChem CID is recorded as 11953806[13].
  • (17R/S)-vomilenine's ChEBI ID is recorded as 16408[14].
  • (17R/S)-vomilenine's found in taxon is recorded as Rauvolfia balansae[15].
  • (17R/S)-vomilenine's found in taxon is recorded as Rauvolfia biauriculata[16].
  • (17R/S)-vomilenine's found in taxon is recorded as Rauvolfia serpentina[17].
  • (17R/S)-vomilenine's Reaxys registry number is recorded as 9588723[18].
  • (17R/S)-vomilenine's Reaxys registry number is recorded as 6985044[19].
  • (17R/S)-vomilenine's Reaxys registry number is recorded as 53093[20].
  • (17R/S)-vomilenine's isomeric SMILES is recorded as C/C=C/1[C@@H]2C[C@H]3C4=NC5=CC=CC=C5[C@]46CC@@HN3[C@@H]1OC@@HN3[C@@H]1O">[21].
  • (17R/S)-vomilenine's KNApSAcK ID is recorded as C00024322[22].
  • (17R/S)-vomilenine's KNApSAcK ID is recorded as C00024338[23].
  • (17R/S)-vomilenine's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+350.163043'}[24].
  • (17R/S)-vomilenine's SureChEMBL ID is recorded as 4411718[25].
  • (17R/S)-vomilenine's UniChem compound ID is recorded as 1074122[26].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . PubChem. Retrieved . wikidata.org.
  3. [4] ↑ . PubChem. Retrieved . wikidata.org.
  4. [5] ↑ . PubChem. Retrieved . wikidata.org.
  5. [6] ↑ . PubChem. Retrieved . wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . Gene Ontology release 2020-05-02. wikidata.org.
  8. [9] ↑ . Gene Ontology release 2020-05-02. wikidata.org.
  9. [10] ↑ . Gene Ontology release 2020-05-02. wikidata.org.
  10. [11] ↑ . Gene Ontology release 2020-05-02. wikidata.org.
  11. [12] ↑ . Q2311683. Retrieved . wikidata.org.
  12. [13] ↑ . PubChem. Retrieved . wikidata.org.
  13. [14] ↑ . ChEBI. Retrieved . wikidata.org.
  14. [15] ↑ . Indole alkaloids from Rauvolfia media. wikidata.org.
  15. [16] ↑ . Indole alkaloids from Rauvolfia media. wikidata.org.
  16. [17] ↑ . Alkaloid Formation in Hairy Roots and Cell Suspensions ofRauwolfia serpentinaBenth. wikidata.org.
  17. [18] ↑ . ChEBI. Retrieved . wikidata.org.
  18. [19] ↑ . ChEBI. Retrieved . wikidata.org.
  19. [20] ↑ . ChEBI. Retrieved . wikidata.org.
  20. [21] ↑ . PubChem. Retrieved . wikidata.org.
  21. [22] ↑ . ChEBI. Retrieved . wikidata.org.
  22. [23] ↑ . ChEBI. Retrieved . wikidata.org.
  23. [24] ↑ . PubChem. Retrieved . wikidata.org.
  24. [25] ↑ . wikidata.org.
  25. [26] ↑ . UniChem. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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APA 4ort.xyz Knowledge Graph. (2026). (17R/S)-vomilenine. Retrieved May 3, 2026, from https://4ort.xyz/entity/-17r-s-vomilenine
MLA “(17R/S)-vomilenine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/-17r-s-vomilenine.
BibTeX @misc{4ortxyz_-17r-s-vomilenine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{(17R/S)-vomilenine}}, year = {2026}, url = {https://4ort.xyz/entity/-17r-s-vomilenine}, note = {Accessed: 2026-05-03}}
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