(+/-)-Huperzine A

group of stereoisomers with the chemical formula C₁₅H₁₈N₂O
ChemicalSubstance group_of_stereoisomers Q105382024
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(+/-)-Huperzine A

Summary

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

Key Facts

  • (+/-)-Huperzine A's instance of is recorded as group of stereoisomers[2].
  • (+/-)-Huperzine A's CAS Registry Number is recorded as 120786-18-7[3].
  • (+/-)-Huperzine A's canonical SMILES is recorded as OC=1N=C2C(=CC1)C3(N)C(=CC)C(C=C(C)C3)C2[4].
  • (+/-)-Huperzine A's InChI is recorded as InChI=1S/C15H18N2O/c1-3-11-10-6-9(2)8-15(11,16)12-4-5-14(18)17-13(12)7-10/h3-6,10H,7-8,16H2,1-2H3,(H,17,18)/b11-3+[5].
  • (+/-)-Huperzine A's InChIKey is recorded as ZRJBHWIHUMBLCN-QDEBKDIKSA-N[6].
  • (+/-)-Huperzine A's chemical formula is recorded as C₁₅H₁₈N₂O[7].
  • (+/-)-Huperzine A's subclass of is recorded as 1-ethyl-2,4-dimethylcyclohexane monoterpenoids[8].
  • (+/-)-Huperzine A's subclass of is recorded as alkaloid[9].
  • (+/-)-Huperzine A's PubChem CID is recorded as 5912039[10].
  • (+/-)-Huperzine A's found in taxon is recorded as Huperzia[11].
  • (+/-)-Huperzine A's found in taxon is recorded as Streptomyces coelicoflavus[12].
  • (+/-)-Huperzine A's isomeric SMILES is recorded as C/C=C1\C2C=C(C)CC1(N)c1ccc(O)nc1C2[13].
  • (+/-)-Huperzine A's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+242.141913196'}[14].
  • (+/-)-Huperzine A's SureChEMBL ID is recorded as 679315[15].
  • (+/-)-Huperzine A's DSSTox substance ID is recorded as DTXSID801115670[16].
  • (+/-)-Huperzine A's MassBank accession ID is recorded as MSBNK-Washington_State_Univ-BML82490[17].
  • (+/-)-Huperzine A's MassBank accession ID is recorded as MSBNK-RIKEN_NPDepo-NGA03129[18].
  • (+/-)-Huperzine A's MassBank accession ID is recorded as MSBNK-RIKEN_NPDepo-NGA03130[19].
  • (+/-)-Huperzine A's MassBank accession ID is recorded as MSBNK-RIKEN_NPDepo-NGA03131[20].
  • (+/-)-Huperzine A's MassBank accession ID is recorded as MSBNK-RIKEN_NPDepo-NGA03132[21].
  • (+/-)-Huperzine A's UniChem compound ID is recorded as 24468876[22].
  • (+/-)-Huperzine A's Probes And Drugs ID is recorded as PD008704[23].

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] . Huperzine A production byPaecilomyces tenuisYS-13, an endophytic fungus isolated fromHuperzia serrata. wikidata.org.
  11. [12] . Taxonomy of the Streptomyces strain ZG0656 that produces acarviostatin alpha-amylase inhibitors and analysis of their effects on blood glucose levels in mammalian systems. wikidata.org.
  12. [13] . wikidata.org.
  13. [14] . wikidata.org.
  14. [15] . wikidata.org.
  15. [16] . wikidata.org.
  16. [17] . MassBank/MassBank-data: release version 2022.06 to wikidata. Retrieved . wikidata.org.
  17. [18] . MassBank/MassBank-data: release version 2022.06 to wikidata. Retrieved . wikidata.org.
  18. [19] . MassBank/MassBank-data: release version 2022.06 to wikidata. Retrieved . wikidata.org.
  19. [20] . MassBank/MassBank-data: release version 2022.06 to wikidata. Retrieved . wikidata.org.
  20. [21] . MassBank/MassBank-data: release version 2022.06 to wikidata. Retrieved . wikidata.org.
  21. [22] . UniChem. wikidata.org.
  22. [23] . wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

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APA 4ort.xyz Knowledge Graph. (2026). (+/-)-Huperzine A. Retrieved May 3, 2026, from https://4ort.xyz/entity/-huperzine-a
MLA “(+/-)-Huperzine A.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/-huperzine-a.
BibTeX @misc{4ortxyz_-huperzine-a_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{(+/-)-Huperzine A}}, year = {2026}, url = {https://4ort.xyz/entity/-huperzine-a}, note = {Accessed: 2026-05-03}}
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