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Alamethicin

chemical compound
ChemicalSubstance type_of_chemical_entity Q4705902
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Alamethicin

Summary

Alamethicin is a type of chemical entity[1]. Alamethicin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (8 views/month).[2]

Key Facts

  • Alamethicin's instance of is recorded as type of chemical entity[3].
  • Alamethicin's chemical structure is recorded as Alamethicin.png[4].
  • Alamethicin's CAS Registry Number is recorded as 27061-78-5[5].
  • Alamethicin's EC number is recorded as 608-040-6[6].
  • Alamethicin's canonical SMILES is recorded as CC(=O)NC(C)(C)C(=O)N1CCCC1C(=O)NC(C)(C)C(=O)NC(C)C(=O)NC(C)(C)C(=O)NC(C)C(=O)NC(CCC(N)=O)C(=O)NC(C)(C)C(=O)NC(C(=O)NC(C)(C)C(=O)NCC(=O)NC(CC(C)C)C(=O)NC(C)(C)C(=O)N1CCCC1C(=O)NC(C(=O)NC(C)(C)C(=O)NC(C)(C)C(=O)NC(CCC(=O)O)C(=O)NC(CCC(N)=O)C(=O)NC(CO)Cc1ccccc1)C(C)C)C(C)C[7].
  • Alamethicin's InChI is recorded as InChI=1S/C92H150N22O25/c1-47(2)43-58(72(127)108-92(24,25)84(139)113-41-29-33-59(113)73(128)103-65(48(3)4)75(130)111-90(20,21)82(137)112-89(18,19)80(135)102-56(37-40-64(120)121)70(125)101-55(35-38-61(93)117)69(124)98-54(46-115)44-53-31-27-26-28-32-53)99-63(119)45-95-77(132)85(10,11)110-76(131)66(49(5)6)104-81(136)88(16,17)107-71(126)57(36-39-62(94)118)100-67(122)50(7)96-78(133)86(12,13)106-68(123)51(8)97-79(134)87(14,15)109-74(129)60-34-30-42-114(60)83(138)91(22,23)105-52(9)116/h26-28,31-32,47-51,54-60,65-66,115H,29-30,33-46H2,1-25H3,(H2,93,117)(H2,94,118)(H,95,132)(H,96,133)(H,97,134)(H,98,124)(H,99,119)(H,100,122)(H,101,125)(H,102,135)(H,103,128)(H,104,136)(H,105,116)(H,106,123)(H,107,126)(H,108,127)(H,109,129)(H,110,131)(H,111,130)(H,112,137)(H,120,121)/t50-,51-,54-,55-,56-,57-,58-,59-,60-,65-,66-/m0/s1[8].
  • Alamethicin's InChIKey is recorded as NRRXBXXRKXUIFD-ZTEFGAJGSA-N[9].
  • Alamethicin's chemical formula is recorded as C₉₂H₁₅₀N₂₂O₂₅[10].
  • Alamethicin's subclass of is recorded as nonribosomal peptide[11].
  • Alamethicin's part of is recorded as peptaibol family[12].
  • Alamethicin's MeSH descriptor ID is recorded as D000408[13].
  • Alamethicin's ChEMBL ID is recorded as CHEMBL438243[14].
  • Alamethicin's Freebase ID is recorded as /m/0276_m[15].
  • Alamethicin's UNII is recorded as 0LT1I1B7S8[16].
  • Alamethicin's ChemSpider ID is recorded as 17288702[17].
  • Alamethicin's PubChem CID is recorded as 16132042[18].
  • Alamethicin's PubChem CID is recorded as 76958618[19].
  • Alamethicin's MeSH tree code is recorded as D04.345.566.040[20].
  • Alamethicin's MeSH tree code is recorded as D12.644.504.111[21].
  • Alamethicin's MeSH tree code is recorded as D12.644.641.040[22].
  • Alamethicin's isomeric SMILES is recorded as CC(C)CC@@HNC(=O)CNC(=O)C(C)(C)NC(=O)C@HNC(=O)C(C)(C)NC(=O)C@HNC(=O)C@HNC(=O)C(C)(C)NC(=O)C@HNC(=O)C(C)(C)NC(=O)[C@@H]3CCCN3C(=O)C(C)(C)NC(=O)CC@@HN">[23].
  • Alamethicin's mass is recorded as {'unit': 'Q483261', 'amount': '+1963.114248299999'}[24].
  • Alamethicin's ECHA Substance Infocard ID is recorded as 100.121.626[25].
  • Alamethicin's subject has role is recorded as antibiotic[26].
  • Alamethicin's subject has role is recorded as ionophore[27].

Why It Matters

Alamethicin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (8 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] ↑ . wikidata.org.
  4. [6] ↑ . ECHA Substance Infocard database. Retrieved . wikidata.org.
  5. [7] ↑ . wikidata.org.
  6. [8] ↑ . wikidata.org.
  7. [9] ↑ . wikidata.org.
  8. [10] ↑ . PubChem. 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] ↑ . wikidata.org.
  20. [22] ↑ . wikidata.org.
  21. [23] ↑ . wikidata.org.
  22. [24] ↑ . wikidata.org.
  23. [25] ↑ . ECHA Substance Infocard database. Retrieved . wikidata.org.
  24. [26] ↑ . Medical Subject Headings. Retrieved . wikidata.org.
  25. [27] ↑ . Medical Subject Headings. Retrieved . 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). Alamethicin. Retrieved May 3, 2026, from https://4ort.xyz/entity/alamethicin
MLA “Alamethicin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/alamethicin.
BibTeX @misc{4ortxyz_alamethicin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Alamethicin}}, year = {2026}, url = {https://4ort.xyz/entity/alamethicin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Alamethicin — https://4ort.xyz/entity/alamethicin (retrieved 2026-05-03)

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