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ageliferin

chemical compound
ChemicalSubstance type_of_chemical_entity Q4691976
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ageliferin

Summary

ageliferin is a type of chemical entity[1]. ageliferin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (4 views/month).[2]

Key Facts

  • ageliferin's instance of is recorded as type of chemical entity[3].
  • ageliferin's chemical structure is recorded as Ageliferin.png[4].
  • ageliferin's CAS Registry Number is recorded as 117417-64-8[5].
  • ageliferin's canonical SMILES is recorded as O=C(NCC1CC=2NC(=N)NC2C(C3=CNC(=N)N3)C1CNC(=O)C4=CC(Br)=CN4)C5=CC(Br)=CN5[6].
  • ageliferin's InChI is recorded as InChI=1S/C22H24Br2N10O2/c23-10-2-14(27-5-10)19(35)29-4-9-1-13-18(34-22(26)32-13)17(16-8-31-21(25)33-16)12(9)7-30-20(36)15-3-11(24)6-28-15/h2-3,5-6,8-9,12,17,27-28H,1,4,7H2,(H,29,35)(H,30,36)(H3,25,31,33)(H3,26,32,34)/t9-,12-,17-/m1/s1[7].
  • ageliferin's InChIKey is recorded as DMMLTRAQSJWUHT-OGTWGDGJSA-N[8].
  • ageliferin's chemical formula is recorded as C₂₂H₂₄Br₂N₁₀O₂[9].
  • ageliferin's subclass of is recorded as N,N'-[[[2-Amino-4-(2-amino-1H-imidazol-5-yl)-4,5,6,7-tetrahydro-1H-benzimidazole]-5,6-diyl]bis(methylene)]bis(4-bromo-1H-pyrrole-2-carboxamide)[10].
  • ageliferin's has part is recorded as carbon[11].
  • ageliferin's has part is recorded as hydrogen[12].
  • ageliferin's has part is recorded as bromine[13].
  • ageliferin's has part is recorded as nitrogen[14].
  • ageliferin's has part is recorded as oxygen[15].
  • ageliferin's ChEMBL ID is recorded as CHEMBL502866[16].
  • ageliferin's Freebase ID is recorded as /m/05h3cpp[17].
  • ageliferin's ChemSpider ID is recorded as 9344613[18].
  • ageliferin's PubChem CID is recorded as 11169518[19].
  • ageliferin's PubChem CID is recorded as 135857532[20].
  • ageliferin's found in taxon is recorded as Agelas[21].
  • ageliferin's found in taxon is recorded as Stylissa caribica[22].
  • ageliferin's found in taxon is recorded as Agelas conifera[23].
  • ageliferin's found in taxon is recorded as Agelas novaecaledoniae[24].
  • ageliferin's found in taxon is recorded as Agelas nakamurai[25].
  • ageliferin's isomeric SMILES is recorded as C1C@@HCNC(=O)C5=CC(=CN5)BrC@@HCNC(=O)C5=CC(=CN5)Br">[26].
  • ageliferin's mass is recorded as {'unit': 'Q483261', 'amount': '+618.045044208'}[27].

Why It Matters

ageliferin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (4 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] ↑ . CAS Common Chemistry. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] ↑ . wikidata.org.
  5. [7] ↑ . PubChem. wikidata.org.
  6. [8] ↑ . PubChem. wikidata.org.
  7. [9] ↑ . PubChem. wikidata.org.
  8. [10] ↑ . wikidata.org.
  9. [11] ↑ . wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . wikidata.org.
  13. [15] ↑ . wikidata.org.
  14. [16] ↑ . wikidata.org.
  15. [17] ↑ . wikidata.org.
  16. [18] ↑ . wikidata.org.
  17. [19] ↑ . wikidata.org.
  18. [20] ↑ . wikidata.org.
  19. [21] ↑ . Ageliferins, potent actomyosin Atpase activators from the Okinawan marine sponge sp. wikidata.org.
  20. [22] ↑ . New Antifeedant Bromopyrrole Alkaloid from the Caribbean Sponge Stylissa caribica. wikidata.org.
  21. [23] ↑ . Bioactive bromopyrrole metabolites from the Caribbean sponge Agelas conifera. wikidata.org.
  22. [24] ↑ . Naturally occurring somatostatin and vasoactive intestinal peptide inhibitors. Isolation of alkaloids from two marine sponges.. wikidata.org.
  23. [25] ↑ . New bromopyrrole alkaloids from the Indopacific sponge Agelas nakamurai. wikidata.org.
  24. [26] ↑ . Retrieved . wikidata.org.
  25. [27] ↑ . 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). ageliferin. Retrieved May 3, 2026, from https://4ort.xyz/entity/ageliferin
MLA “ageliferin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/ageliferin.
BibTeX @misc{4ortxyz_ageliferin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{ageliferin}}, year = {2026}, url = {https://4ort.xyz/entity/ageliferin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): ageliferin — https://4ort.xyz/entity/ageliferin (retrieved 2026-05-03)

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