Alamethicin
chemical compound
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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 (42 views/month).[2]
Key Facts
- Alamethicin's instance of is recorded as type of chemical entity[3].
- 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[4].
- Alamethicin's chemical formula is recorded as C₉₂H₁₅₀N₂₂O₂₅[5].
- Alamethicin is a type of nonribosomal peptide[6].
- Alamethicin is part of peptaibol family[7].
- 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">[8].
- Alamethicin's mass is recorded as {'unit': 'Q483261', 'amount': '+1963.114248299999'}[9].
- Alamethicin's subject has role is recorded as antibiotic[10].
- Alamethicin's subject has role is recorded as ionophore[11].
- Alamethicin's subject has role is recorded as uncoupling agents[12].
Why It Matters
Alamethicin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (42 views/month).[2]