(+)-Mahanimbicine

group of stereoisomers with the chemical formula C₂₃H₂₅NO
ChemicalSubstance group_of_stereoisomers Q105369108
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(+)-Mahanimbicine

Summary

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

Key Facts

  • (+)-Mahanimbicine's instance of is recorded as group of stereoisomers[2].
  • (+)-Mahanimbicine's CAS Registry Number is recorded as 28305-77-3[3].
  • (+)-Mahanimbicine's canonical SMILES is recorded as O1C=2C=CC=3C4=CC(=CC=C4NC3C2C=CC1(C)CCC=C(C)C)C[4].
  • (+)-Mahanimbicine's InChI is recorded as InChI=1S/C23H25NO/c1-15(2)6-5-12-23(4)13-11-18-21(25-23)10-8-17-19-14-16(3)7-9-20(19)24-22(17)18/h6-11,13-14,24H,5,12H2,1-4H3[5].
  • (+)-Mahanimbicine's InChIKey is recorded as YZBKHDJPIAYXQH-UHFFFAOYSA-N[6].
  • (+)-Mahanimbicine's chemical formula is recorded as C₂₃H₂₅NO[7].
  • (+)-Mahanimbicine's subclass of is recorded as 2,6-dimethyloctane monoterpenoid[8].
  • (+)-Mahanimbicine's subclass of is recorded as carbazole alkaloid[9].
  • (+)-Mahanimbicine's PubChem CID is recorded as 4072580[10].
  • (+)-Mahanimbicine's ChEBI ID is recorded as 179459[11].
  • (+)-Mahanimbicine's found in taxon is recorded as Murraya koenigii[12].
  • (+)-Mahanimbicine's Human Metabolome Database ID is recorded as HMDB0030225[13].
  • (+)-Mahanimbicine's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+331.19361442'}[14].
  • (+)-Mahanimbicine's SureChEMBL ID is recorded as 30125689[15].
  • (+)-Mahanimbicine's DSSTox substance ID is recorded as DTXSID901317689[16].
  • (+)-Mahanimbicine's UniChem compound ID is recorded as 32003720[17].

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] . wikidata.org.
  9. [10] . PubChem. Retrieved . wikidata.org.
  10. [11] . ChEBI release 2022-06-13. wikidata.org.
  11. [12] . Alkaloids from Sri Lankan curry-leaf (Murraya koenigii) display melanogenesis inhibitory activity: structures of karapinchamines A and B.. wikidata.org.
  12. [13] . wikidata.org.
  13. [14] . wikidata.org.
  14. [15] . wikidata.org.
  15. [16] . wikidata.org.
  16. [17] . UniChem. 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). (+)-Mahanimbicine. Retrieved May 3, 2026, from https://4ort.xyz/entity/-mahanimbicine
MLA “(+)-Mahanimbicine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/-mahanimbicine.
BibTeX @misc{4ortxyz_-mahanimbicine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{(+)-Mahanimbicine}}, year = {2026}, url = {https://4ort.xyz/entity/-mahanimbicine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): (+)-Mahanimbicine — https://4ort.xyz/entity/-mahanimbicine (retrieved 2026-05-03)

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