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tetrandrine

chemical compound
ChemicalSubstance type_of_chemical_entity Q7706612
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tetrandrine

Summary

tetrandrine is a type of chemical entity[1]. tetrandrine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (18 views/month).[2]

Key Facts

  • tetrandrine's instance of is recorded as type of chemical entity[3].
  • tetrandrine's CAS Registry Number is recorded as 518-34-3[4].
  • tetrandrine's EC number is recorded as 683-095-7[5].
  • tetrandrine's canonical SMILES is recorded as CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)OC)OC[6].
  • tetrandrine's InChI is recorded as InChI=1S/C38H42N2O6/c1-39-15-13-25-20-32(42-4)34-22-28(25)29(39)17-23-7-10-27(11-8-23)45-33-19-24(9-12-31(33)41-3)18-30-36-26(14-16-40(30)2)21-35(43-5)37(44-6)38(36)46-34/h7-12,19-22,29-30H,13-18H2,1-6H3/t29-,30-/m0/s1[7].
  • tetrandrine's InChIKey is recorded as WVTKBKWTSCPRNU-KYJUHHDHSA-N[8].
  • tetrandrine's chemical formula is recorded as C₃₈H₄₂N₂O₆[9].
  • tetrandrine's subclass of is recorded as isoquinoline alkaloid[10].
  • tetrandrine's MeSH descriptor ID is recorded as C009438[11].
  • tetrandrine's ChEMBL ID is recorded as CHEMBL176045[12].
  • tetrandrine's Freebase ID is recorded as /m/0547h0z[13].
  • tetrandrine's UNII is recorded as 29EX23D5AJ[14].
  • tetrandrine's UNII is recorded as VS4W77H3SD[15].
  • tetrandrine's RTECS number is recorded as XE9350000[16].
  • tetrandrine's ChemSpider ID is recorded as 4479515[17].
  • tetrandrine's PubChem CID is recorded as 73078[18].
  • tetrandrine's KEGG ID is recorded as C09654[19].
  • tetrandrine's ChEBI ID is recorded as 49[20].
  • tetrandrine's found in taxon is recorded as Cocculus pendulus[21].
  • tetrandrine's found in taxon is recorded as Stephania tetrandra[22].
  • tetrandrine's found in taxon is recorded as Menispermaceae[23].
  • tetrandrine's found in taxon is recorded as Cyclea peltata[24].
  • tetrandrine's found in taxon is recorded as Menispermum dauricum[25].
  • tetrandrine's found in taxon is recorded as Pachygone dasycarpa[26].
  • tetrandrine's found in taxon is recorded as Triclisia patens[27].

Why It Matters

tetrandrine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (18 views/month).[2] tetrandrine has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[28] tetrandrine is known by 7 alternative names across languages and contexts.[29]

References

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

Direct Wikidata claims

  1. [3] ↑ . wikidata.org.
  2. [4] ↑ . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  3. [5] ↑ . ECHA Substance Infocard database. Retrieved . wikidata.org.
  4. [6] ↑ . PubChem. Retrieved . wikidata.org.
  5. [7] ↑ . PubChem. Retrieved . wikidata.org.
  6. [8] ↑ . PubChem. Retrieved . wikidata.org.
  7. [9] ↑ . PubChem. Retrieved . wikidata.org.
  8. [10] ↑ . wikidata.org.
  9. [11] ↑ . Medical Subject Headings. Retrieved . wikidata.org.
  10. [12] ↑ . ChEMBL. Retrieved . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  13. [15] ↑ . wikidata.org.
  14. [16] ↑ . wikidata.org.
  15. [17] ↑ . wikidata.org.
  16. [18] ↑ . PubChem. Retrieved . wikidata.org.
  17. [19] ↑ . ChEBI. Retrieved . wikidata.org.
  18. [20] ↑ . ChEMBL. Retrieved . wikidata.org.
  19. [21] ↑ . Alkaloids of Cocculus pendulus. wikidata.org.
  20. [22] ↑ . A 4,5-Dioxoaporphine from the Aerial Parts of Stephania tetrandra. wikidata.org.
  21. [23] ↑ . Tetrandrine inhibits proinflammatory cytokines, iNOS and COX-2 expression in human monocytic cells. wikidata.org.
  22. [24] ↑ . Isolation of Phaeanthine from Cyclea burmanni. wikidata.org.
  23. [25] ↑ . Studies on constituents of medicinal plants. XXIII. Constituents of the vines of Menispermum dauricum DC. 2.. wikidata.org.
  24. [26] ↑ . (+)-Angchibangkine, a new type of bisbenzylisoquinoline alkaloid, and other dimers from Pachygone dasycarpa. wikidata.org.
  25. [27] ↑ . Additional alkaloids of Triclisia patens and Triclisia subcordata. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] ↑ . Wikidata sitelinks. wikidata.org.
  3. [29] ↑ . Wikidata aliases. 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). tetrandrine. Retrieved May 3, 2026, from https://4ort.xyz/entity/tetrandrine
MLA “tetrandrine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/tetrandrine.
BibTeX @misc{4ortxyz_tetrandrine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{tetrandrine}}, year = {2026}, url = {https://4ort.xyz/entity/tetrandrine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): tetrandrine — https://4ort.xyz/entity/tetrandrine (retrieved 2026-05-03)

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