asperlicin

chemical compound
ChemicalSubstance type_of_chemical_entity Q4807912
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asperlicin

Summary

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

Key Facts

  • asperlicin's instance of is recorded as type of chemical entity[3].
  • asperlicin's chemical structure is recorded as Asperlicin structure.svg[4].
  • asperlicin's CAS Registry Number is recorded as 93413-04-8[5].
  • asperlicin's canonical SMILES is recorded as CC(C)CC1C(=O)N2C(N1)C(C3=CC=CC=C32)(CC4C5=NC6=CC=CC=C6C(=O)N5C7=CC=CC=C7C(=O)N4)O[6].
  • asperlicin's InChI is recorded as InChI=1S/C31H29N5O4/c1-17(2)15-22-29(39)36-25-14-8-5-11-20(25)31(40,30(36)34-22)16-23-26-32-21-12-6-3-9-18(21)28(38)35(26)24-13-7-4-10-19(24)27(37)33-23/h3-14,17,22-23,30,34,40H,15-16H2,1-2H3,(H,33,37)/t22-,23-,30-,31-/m0/s1[7].
  • asperlicin's InChIKey is recorded as MGMRIOLWEROPJY-FPACPZPDSA-N[8].
  • asperlicin's chemical formula is recorded as C₃₁H₂₉N₅O₄[9].
  • asperlicin's subclass of is recorded as (7S)-7-[[(2S,4S)-4-hydroxy-2-(2-methylpropyl)-1-oxo-3,3a-dihydro-2H-imidazo[1,2-a]indol-4-yl]methyl]-6,7-dihydroquinazolino[3,2-a][1,4]benzodiazepine-5,13-dione[10].
  • asperlicin's Commons category is recorded as Asperlicin[11].
  • asperlicin's MeSH descriptor ID is recorded as C046367[12].
  • asperlicin's ChEMBL ID is recorded as CHEMBL283117[13].
  • asperlicin's Freebase ID is recorded as /m/04zxtkw[14].
  • asperlicin's UNII is recorded as U0MJE9LRXV[15].
  • asperlicin's ChemSpider ID is recorded as 2299674[16].
  • asperlicin's PubChem CID is recorded as 3035433[17].
  • asperlicin's found in taxon is recorded as Aspergillus alliaceus[18].
  • asperlicin's isomeric SMILES is recorded as CC(C)C[C@H]1C(=O)N2C@HC@@(C[C@H]4C5=NC6=CC=CC=C6C(=O)N5C7=CC=CC=C7C(=O)N4)OC@HC@@(C[C@H]4C5=NC6=CC=CC=C6C(=O)N5C7=CC=CC=C7C(=O)N4)O">[19].
  • asperlicin's mass is recorded as {'unit': 'Q483261', 'amount': '+535.222'}[20].
  • asperlicin's subject has role is recorded as hormone antagonist[21].
  • asperlicin's SureChEMBL ID is recorded as 1004269[22].
  • asperlicin's UMLS CUI is recorded as C0052553[23].
  • asperlicin's DSSTox substance ID is recorded as DTXSID20918456[24].
  • asperlicin's Microsoft Academic ID is recorded as 2778684560[25].
  • asperlicin's DSSTOX compound identifier is recorded as DTXCID901347406[26].
  • asperlicin's UniChem compound ID is recorded as 102157[27].

Why It Matters

asperlicin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (6 views/month).[2]

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] . 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] . wikidata.org.
  10. [12] . Medical Subject Headings. Retrieved . wikidata.org.
  11. [13] . ChEMBL. Retrieved . wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . Global Substance Registration System. Retrieved . wikidata.org.
  14. [16] . Q2311683. Retrieved . wikidata.org.
  15. [17] . PubChem. Retrieved . wikidata.org.
  16. [18] . History of yield improvements in the production of asperlicin byAspergillus alliaceus. wikidata.org.
  17. [19] . PubChem. Retrieved . wikidata.org.
  18. [20] . PubChem. Retrieved . wikidata.org.
  19. [21] . Medical Subject Headings. Retrieved . wikidata.org.
  20. [22] . wikidata.org.
  21. [23] . UMLS 2023. Retrieved . wikidata.org.
  22. [24] . wikidata.org.
  23. [25] . wikidata.org.
  24. [26] . wikidata.org.
  25. [27] . UniChem. wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.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). asperlicin. Retrieved May 3, 2026, from https://4ort.xyz/entity/asperlicin
MLA “asperlicin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/asperlicin.
BibTeX @misc{4ortxyz_asperlicin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{asperlicin}}, year = {2026}, url = {https://4ort.xyz/entity/asperlicin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): asperlicin — https://4ort.xyz/entity/asperlicin (retrieved 2026-05-03)

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