silibinin A

chemical compound
ChemicalSubstance type_of_chemical_entity Q425702
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silibinin A

Summary

silibinin An is a type of chemical entity[1]. It ranks in the top 5% of type_of_chemical_entity entities by monthly Wikipedia readership (175 views/month).[2]

Key Facts

  • silibinin A's instance of is recorded as type of chemical entity[3].
  • silibinin A's chemical structure is recorded as Silibinin skeletal.svg[4].
  • silibinin A's CAS Registry Number is recorded as 22888-70-6[5].
  • silibinin A's EC number is recorded as 245-302-5[6].
  • silibinin A's canonical SMILES is recorded as COC1=C(C=CC(=C1)C2C(OC3=C(O2)C=C(C=C3)C4C(C(=O)C5=C(C=C(C=C5O4)O)O)O)CO)O[7].
  • silibinin A's InChI is recorded as InChI=1S/C25H22O10/c1-32-17-6-11(2-4-14(17)28)24-20(10-26)33-16-5-3-12(7-18(16)34-24)25-23(31)22(30)21-15(29)8-13(27)9-19(21)35-25/h2-9,20,23-29,31H,10H2,1H3/t20-,23+,24-,25-/m1/s1[8].
  • silibinin A's InChIKey is recorded as SEBFKMXJBCUCAI-HKTJVKLFSA-N[9].
  • silibinin A's ATC code is recorded as A05BA03[10].
  • silibinin A's chemical formula is recorded as C₂₅H₂₂O₁₀[11].
  • silibinin A's subclass of is recorded as 2-[2R,3R-Dihydro-3-(4-hydroxy-3-methoxyphenyl)-2-(hydroxymethyl)-1,4-benzodioxin-6-yl]-2R,3R-dihydro-3,5,7-trihydroxy-4H-1-benzopyran-4-one[12].
  • silibinin A's MeSH descriptor ID is recorded as D000077385[13].
  • silibinin A's ChEMBL ID is recorded as CHEMBL431701[14].
  • silibinin A's Freebase ID is recorded as /m/05fjw2[15].
  • silibinin A's UNII is recorded as 33X338MNE4[16].
  • silibinin A's ChemSpider ID is recorded as 29263[17].
  • silibinin A's PubChem CID is recorded as 31553[18].
  • silibinin A's KEGG ID is recorded as D08515[19].
  • silibinin A's KEGG ID is recorded as C07610[20].
  • silibinin A's MeSH tree code is recorded as D03.383.663.283.266.450.268.777.500[21].
  • silibinin A's MeSH tree code is recorded as D03.633.100.150.266.450.268.777.500[22].
  • silibinin A's ChEBI ID is recorded as 9144[23].
  • silibinin A's found in taxon is recorded as Homo sapiens[24].
  • silibinin A's found in taxon is recorded as Silybum marianum[25].
  • silibinin A's found in taxon is recorded as Asteraceae[26].
  • silibinin A's found in taxon is recorded as Anastatica hierochuntica[27].

Why It Matters

silibinin A ranks in the top 5% of type_of_chemical_entity entities by monthly Wikipedia readership (175 views/month).[2] It has Wikipedia articles in 14 language editions, a strong signal of global cultural recognition.[28] It is known by 21 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] . wikidata.org.
  3. [5] . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] . Global Substance Registration System. 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] . PubChem. Retrieved . wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . ChEMBL. Retrieved . wikidata.org.
  13. [15] . Freebase Data Dumps. wikidata.org.
  14. [16] . Global Substance Registration System. Retrieved . wikidata.org.
  15. [17] . Q2311683. Retrieved . wikidata.org.
  16. [18] . PubChem. Retrieved . wikidata.org.
  17. [19] . ChEBI. Retrieved . wikidata.org.
  18. [20] . ChEBI. Retrieved . wikidata.org.
  19. [21] . wikidata.org.
  20. [22] . wikidata.org.
  21. [23] . ChEBI. Retrieved . wikidata.org.
  22. [24] . WikiPathways. Retrieved . identifiers.org. Provenance: wikidata.org.
  23. [25] . A simple device allowing UV-detection of the active substances of Silybum marianum (L.) Gaertner on TLC plates devoid of fluorescent indicator. wikidata.org.
  24. [26] . Therapeutic effects of silibinin on LPS-induced acute lung injury by inhibiting NLRP3 and NF-κB signaling pathways. wikidata.org.
  25. [27] . Melanogenesis inhibitors from the desert plant Anastatica hierochuntica in B16 melanoma cells. 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). silibinin A. Retrieved May 3, 2026, from https://4ort.xyz/entity/silibinin-a
MLA “silibinin A.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/silibinin-a.
BibTeX @misc{4ortxyz_silibinin-a_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{silibinin A}}, year = {2026}, url = {https://4ort.xyz/entity/silibinin-a}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): silibinin A — https://4ort.xyz/entity/silibinin-a (retrieved 2026-05-03)

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