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eptifibatide

chemical compound
ChemicalSubstance type_of_chemical_entity Q2295855
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eptifibatide

Summary

eptifibatide is a type of chemical entity[1]. eptifibatide ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (29 views/month).[2]

Key Facts

  • eptifibatide's instance of is recorded as type of chemical entity[3].
  • eptifibatide's chemical structure is recorded as Eptifibatide structure.svg[4].
  • eptifibatide's physically interacts with is recorded as integrin subunit alpha 2b[5].
  • eptifibatide's physically interacts with is recorded as Integrin subunit beta 3[6].
  • eptifibatide's CAS Registry Number is recorded as 188627-80-7[7].
  • eptifibatide's EC number is recorded as 641-366-7[8].
  • eptifibatide's canonical SMILES is recorded as C1CC2C(=O)NC(CSSCCC(=O)NC(C(=O)NCC(=O)NC(C(=O)NC(C(=O)N2C1)CC3=CNC4=CC=CC=C43)CC(=O)O)CCCCN=C(N)N)C(=O)N[9].
  • eptifibatide's InChI is recorded as InChI=1S/C35H49N11O9S2/c36-30(51)25-18-57-56-13-10-27(47)42-22(8-3-4-11-39-35(37)38)31(52)41-17-28(48)43-23(15-29(49)50)32(53)44-24(14-19-16-40-21-7-2-1-6-20(19)21)34(55)46-12-5-9-26(46)33(54)45-25/h1-2,6-7,16,22-26,40H,3-5,8-15,17-18H2,(H2,36,51)(H,41,52)(H,42,47)(H,43,48)(H,44,53)(H,45,54)(H,49,50)(H4,37,38,39)/t22-,23-,24-,25-,26-/m0/s1[10].
  • eptifibatide's InChIKey is recorded as CZKPOZZJODAYPZ-LROMGURASA-N[11].
  • eptifibatide's ATC code is recorded as B01AC16[12].
  • eptifibatide's chemical formula is recorded as C₃₅H₄₉N₁₁O₉S₂[13].
  • eptifibatide's subclass of is recorded as Integrilin[14].
  • eptifibatide's has use is recorded as medication[15].
  • eptifibatide's MeSH descriptor ID is recorded as D000077542[16].
  • eptifibatide's ChEMBL ID is recorded as CHEMBL1174[17].
  • eptifibatide's Guide to Pharmacology Ligand ID is recorded as 6585[18].
  • eptifibatide's Freebase ID is recorded as /m/0c2jmg[19].
  • eptifibatide's UNII is recorded as NA8320J834[20].
  • eptifibatide's ChemSpider ID is recorded as 10482060[21].
  • eptifibatide's PubChem CID is recorded as 448812[22].
  • eptifibatide's KEGG ID is recorded as D06888[23].
  • eptifibatide's MeSH tree code is recorded as D12.644.641.366[24].
  • eptifibatide's ChEBI ID is recorded as 291902[25].
  • eptifibatide's DrugBank ID is recorded as DB00063[26].
  • eptifibatide's significant drug interaction is recorded as nabumetone[27].

Why It Matters

eptifibatide ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (29 views/month).[2] eptifibatide has Wikipedia articles in 10 language editions, a strong signal of global cultural recognition.[28] eptifibatide is known by 5 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] ↑ . Open Targets Platform. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  4. [6] ↑ . Open Targets Platform. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  5. [7] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  6. [8] ↑ . ECHA Substance Infocard database. Retrieved . wikidata.org.
  7. [9] ↑ . PubChem. Retrieved . wikidata.org.
  8. [10] ↑ . PubChem. Retrieved . wikidata.org.
  9. [11] ↑ . PubChem. Retrieved . wikidata.org.
  10. [12] ↑ . DrugBank. wikidata.org.
  11. [13] ↑ . PubChem. Retrieved . wikidata.org.
  12. [14] ↑ . wikidata.org.
  13. [15] ↑ . wikidata.org.
  14. [16] ↑ . wikidata.org.
  15. [17] ↑ . ChEMBL. Retrieved . wikidata.org.
  16. [18] ↑ . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  17. [19] ↑ . Freebase Data Dumps. wikidata.org.
  18. [20] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  19. [21] ↑ . Q2311683. Retrieved . wikidata.org.
  20. [22] ↑ . PubChem. Retrieved . wikidata.org.
  21. [23] ↑ . ChEBI. Retrieved . wikidata.org.
  22. [24] ↑ . wikidata.org.
  23. [25] ↑ . ChEMBL. Retrieved . wikidata.org.
  24. [26] ↑ . wikidata.org.
  25. [27] ↑ . A reference set of clinically relevant adverse drug-drug interactions. 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). eptifibatide. Retrieved May 3, 2026, from https://4ort.xyz/entity/eptifibatide
MLA “eptifibatide.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/eptifibatide.
BibTeX @misc{4ortxyz_eptifibatide_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{eptifibatide}}, year = {2026}, url = {https://4ort.xyz/entity/eptifibatide}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): eptifibatide — https://4ort.xyz/entity/eptifibatide (retrieved 2026-05-03)

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