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apamin

chemical compound
ChemicalSubstance type_of_chemical_entity Q417260
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apamin

Summary

apamin is a type of chemical entity[1]. apamin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (22 views/month).[2]

Key Facts

  • apamin's instance of is recorded as type of chemical entity[3].
  • apamin's CAS Registry Number is recorded as 24345-16-2[4].
  • apamin's EC number is recorded as 246-182-7[5].
  • apamin's canonical SMILES is recorded as CC1C(=O)NC(C(=O)NC(C(=O)NC(CSSCC2C(=O)NC(C(=O)NC(C(=O)N3CCCC3C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(CSSCC(C(=O)NC(C(=O)N2)CC(=O)N)N)C(=O)N1)CC(C)C)C)C(C)O)CCC(=O)O)C)CCCCN)C(=O)NC(CCC(=O)N)C(=O)NC(CCC(=O)N)C(=O)NC(CC4=CNC=N4)C(=O)N)CCCNC(=N)N)CCCNC(=N)N[6].
  • apamin's InChI is recorded as InChI=1S/C79H131N31O24S4/c1-35(2)26-49-70(127)107-51-31-136-135-30-41(81)63(120)105-50(28-57(84)114)71(128)108-53(73(130)99-42(12-7-8-22-80)64(121)96-38(5)77(134)110-25-11-15-54(110)75(132)102-47(18-21-58(115)116)69(126)109-59(39(6)111)76(133)95-37(4)62(119)104-49)33-138-137-32-52(106-66(123)44(14-10-24-92-79(88)89)98-65(122)43(13-9-23-91-78(86)87)97-61(118)36(3)94-72(51)129)74(131)101-45(16-19-55(82)112)67(124)100-46(17-20-56(83)113)68(125)103-48(60(85)117)27-40-29-90-34-93-40/h29,34-39,41-54,59,111H,7-28,30-33,80-81H2,1-6H3,(H2,82,112)(H2,83,113)(H2,84,114)(H2,85,117)(H,90,93)(H,94,129)(H,95,133)(H,96,121)(H,97,118)(H,98,122)(H,99,130)(H,100,124)(H,101,131)(H,102,132)(H,103,125)(H,104,119)(H,105,120)(H,106,123)(H,107,127)(H,108,128)(H,109,126)(H,115,116)(H4,86,87,91)(H4,88,89,92)/t36-,37-,38-,39+,41-,42-,43-,44-,45-,46-,47-,48-,49-,50-,51-,52-,53-,54-,59-/m0/s1[7].
  • apamin's InChIKey is recorded as YVIIHEKJCKCXOB-STYWVVQQSA-N[8].
  • apamin's chemical formula is recorded as C₇₉H₁₃₁N₃₁O₂₄S₄[9].
  • apamin's subclass of is recorded as peptide[10].
  • apamin's part of is recorded as apitoxin[11].
  • apamin's MeSH descriptor ID is recorded as D001030[12].
  • apamin's ChEMBL ID is recorded as CHEMBL525408[13].
  • apamin's Guide to Pharmacology Ligand ID is recorded as 2311[14].
  • apamin's Freebase ID is recorded as /m/03cjgxs[15].
  • apamin's ChemSpider ID is recorded as 21169555[16].
  • apamin's PubChem CID is recorded as 16133797[17].
  • apamin's PubChem CID is recorded as 16218850[18].
  • apamin's PubChem CID is recorded as 91935372[19].
  • apamin's PubChem CID is recorded as 170844080[20].
  • apamin's MeSH tree code is recorded as D20.888.065.115.060[21].
  • apamin's MeSH tree code is recorded as D23.946.833.065.115.060[22].
  • apamin's isomeric SMILES is recorded as C[C@H]1C(=O)NC@HCCCNC(=N)N[23].
  • apamin's mass is recorded as {'unit': 'Q483261', 'amount': '+2025.886608'}[24].
  • apamin's ECHA Substance Infocard ID is recorded as 100.041.969[25].
  • apamin's subject has role is recorded as neurotoxin[26].
  • apamin's SureChEMBL ID is recorded as 29362415[27].

Why It Matters

apamin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (22 views/month).[2] apamin has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[28] apamin 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] ↑ . ECHA Substance Infocard database. Retrieved . wikidata.org.
  4. [6] ↑ . PubChem. Retrieved . wikidata.org.
  5. [7] ↑ . wikidata.org.
  6. [8] ↑ . PubChem. Retrieved . wikidata.org.
  7. [9] ↑ . PubChem. Retrieved . wikidata.org.
  8. [10] ↑ . wikidata.org.
  9. [11] ↑ . wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . ChEMBL. Retrieved . wikidata.org.
  12. [14] ↑ . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  13. [15] ↑ . Freebase Data Dumps. wikidata.org.
  14. [16] ↑ . Q2311683. Retrieved . wikidata.org.
  15. [17] ↑ . PubChem. Retrieved . wikidata.org.
  16. [18] ↑ . wikidata.org.
  17. [19] ↑ . wikidata.org.
  18. [20] ↑ . wikidata.org.
  19. [21] ↑ . wikidata.org.
  20. [22] ↑ . wikidata.org.
  21. [23] ↑ . PubChem. Retrieved . wikidata.org.
  22. [24] ↑ . PubChem. Retrieved . wikidata.org.
  23. [25] ↑ . ECHA Substance Infocard database. Retrieved . wikidata.org.
  24. [26] ↑ . wikidata.org.
  25. [27] ↑ . 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). apamin. Retrieved May 3, 2026, from https://4ort.xyz/entity/apamin
MLA “apamin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/apamin.
BibTeX @misc{4ortxyz_apamin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{apamin}}, year = {2026}, url = {https://4ort.xyz/entity/apamin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): apamin — https://4ort.xyz/entity/apamin (retrieved 2026-05-03)

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