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schisandrin C

group of stereoisomers with the chemical formula C₂₂H₂₄O₆
ChemicalSubstance group_of_stereoisomers Q105033361
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schisandrin C

Summary

schisandrin C is a group of stereoisomers[1].

Key Facts

  • schisandrin C's instance of is recorded as group of stereoisomers[2].
  • schisandrin C's CAS Registry Number is recorded as 61301-33-5[3].
  • schisandrin C's canonical SMILES is recorded as O(C1=C2OCOC2=CC3=C1C4=C(OC)C=5OCOC5C=C4CC(C)C(C)C3)C[4].
  • schisandrin C's InChI is recorded as InChI=1S/C22H24O6/c1-11-5-13-7-15-19(27-9-25-15)21(23-3)17(13)18-14(6-12(11)2)8-16-20(22(18)24-4)28-10-26-16/h7-8,11-12H,5-6,9-10H2,1-4H3[5].
  • schisandrin C's InChIKey is recorded as HTBWBWWADZJXID-UHFFFAOYSA-N[6].
  • schisandrin C's chemical formula is recorded as C₂₂H₂₄O₆[7].
  • schisandrin C's subclass of is recorded as schisandrin[8].
  • schisandrin C's PubChem CID is recorded as 119112[9].
  • schisandrin C's found in taxon is recorded as Schisandra sphenanthera[10].
  • schisandrin C's found in taxon is recorded as Schisandra chinensis[11].
  • schisandrin C's Human Metabolome Database ID is recorded as HMDB0258167[12].
  • schisandrin C's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+384.157288488'}[13].
  • schisandrin C's SureChEMBL ID is recorded as 12280310[14].
  • schisandrin C's DSSTox substance ID is recorded as DTXSID101317497[15].
  • schisandrin C's UniChem compound ID is recorded as 24295538[16].
  • schisandrin C's Probes And Drugs ID is recorded as PD087592[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] ↑ . PubChem. Retrieved . wikidata.org.
  9. [10] ↑ . A simple and sensitive HPLC method for the simultaneous determination of eight bioactive components and fingerprint analysis of Schisandra sphenanthera. wikidata.org.
  10. [11] ↑ . Induction of the phase II detoxification enzyme NQO1 in hepatocarcinoma cells by lignans from the fruit of Schisandra chinensis through nuclear accumulation of Nrf2.. wikidata.org.
  11. [12] ↑ . wikidata.org.
  12. [13] ↑ . wikidata.org.
  13. [14] ↑ . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . UniChem. wikidata.org.
  16. [17] ↑ . 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). schisandrin C. Retrieved May 3, 2026, from https://4ort.xyz/entity/schisandrin-c
MLA “schisandrin C.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/schisandrin-c.
BibTeX @misc{4ortxyz_schisandrin-c_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{schisandrin C}}, year = {2026}, url = {https://4ort.xyz/entity/schisandrin-c}, note = {Accessed: 2026-05-03}}
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