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62874-51-5

62874-51-5 Structure

62874-51-5 Structure
IdentificationBack Directory
[Name]

4-Amino-1-[[(carbamoylamino)acetyl]methylamino]-1,4-dideoxy-3-O-(2,6-diamino-2,3,4,6,7-pentadeoxy-β-L-lyxo-heptopyranosyl)-6-O-methyl-L-chiro-inositol
[CAS]

62874-51-5
[Synonyms]

Fortimicin C
4-Amino-1-[[(carbamoylamino)acetyl]methylamino]-1,4-dideoxy-3-O-(2,6-diamino-2,3,4,6,7-pentadeoxy-β-L-lyxo-heptopyranosyl)-6-O-methyl-L-chiro-inositol
L-chiro-Inositol, 4-amino-1-[[2-[(aminocarbonyl)amino]acetyl]methylamino]-1,4-dideoxy-3-O-(2,6-diamino-2,3,4,6,7-pentadeoxy-β-L-lyxo-heptopyranosyl)-6-O-methyl-
[Molecular Formula]

C18H36N6O7
[MOL File]

62874-51-5.mol
[Molecular Weight]

448.51
Chemical PropertiesBack Directory
[Boiling point ]

679.5±55.0 °C(Predicted)
[density ]

1.36±0.1 g/cm3(Predicted)
[pka]

12.67±0.46(Predicted)
Hazard InformationBack Directory
[Uses]

Fortimicin C is an antibiotic, which can be isolated from Micromonospora olivoasterospora. Fortimicin C exhibits broad-spectrum antibacterial activity, inhibits Escherichia coli, Staphylococcus aureus, Bacillus subtilis, Klebsiella pneumoniae, Salmonella typhosa and Serratia marcescens, with MICs of 0.16-0.64 μg/mL. Fortimicin C is resistant against aminoglycoside inactivating enzymes[1].
[IC 50]

Aminoglycoside
[References]

[1] Sugimoto M, et al., Fortimicins C, D and KE, new aminoglycoside antibiotics. J Antibiot (Tokyo). 1979 Sep;32(9):868-73. DOI:10.7164/antibiotics.32.868
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