Compound ID | 3012

Update compound information

Fusaricidin

Class: Antimicrobial peptide

Spectrum of activity: Gram-positive
Details of activity: Active against Staphylococcus aureus
Description: Natural product from Bacillus polymyxa KT-8; depsipeptide scaffold
Institute where first reported: Wakunaga Pharmaceutical Co., Ltd.; Institute of Pharmaceutical Sciences, Hiroshima University School of Medicine
Year first mentioned: 1996
Development status: Experimental
Chemical structure(s):
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Molecular weight: 883.09
Iso. SMILES: C[C@@H]1[C@@H](C(=O)N[C@@H](C(=O)N[C@H](C(=O)N[C@@H](C(=O)N[C@@H](C(=O)N[C@@H](C(=O)O1)C)CC(=O)N)[C@@H](C)O)C(C)C)C(C)C)NC(=O)CC(CCCCCCCCCCCCN=C(N)N)O
InChI Key: ZQMLIVBQFXSJNR-NVCIGDDDSA-N
Can. SMILES: CC(C)[C@@H]1C(=O)N[C@@H](C(C)C)C(=O)N[C@H]([C@@H](C)O)C(=O)N[C@H](CC(=O)N)C(=O)N[C@H](C)C(=O)O[C@H](C)[C@@H](C(=O)N1)NC(=O)CC(CCCCCCCCCCCCN=C(N)N)O
InChI: InChI=1S/C41H74N10O11/c1-22(2)31-36(57)49-32(23(3)4)37(58)51-33(25(6)52)38(59)47-28(21-29(42)54)35(56)46-24(5)40(61)62-26(7)34(39(60)50-31)48-30(55)20-27(53)18-16-14-12-10-8-9-11-13-15-17-19-45-41(43)44/h22-28,31-34,52-53H,8-21H2,1-7H3,(H2,42,54)(H,46,56)(H,47,59)(H,48,55)(H,49,57)(H,50,60)(H,51,58)(H4,43,44,45)/t24-,25-,26-,27?,28-,31-,32+,33-,34+/m1/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/21581469
Citations:
  • https://doi.org/10.7164/antibiotics.49.129
  • https://pubmed.ncbi.nlm.nih.gov/24164269/

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