Compound ID | 3247

Update compound information

AC4437

Synonym(s): AC-4437  |  AC 4437

Class: Aminoglycoside

Spectrum of activity: Gram-positive  &  Gram-negative
Details of activity: Active against Staphylococcus aureus, Streptococcus pyogenes, Escherichia coli, Klebsiella pneumoniae, and Salmonella enteritidis
Description: Natural product from Streptomyces sp.; de-N-methyl-L-glucosamine analogue of dihydrostreptomycin
Institute where first reported: Medicinal Research Laboratories, Toyo Jozo Co., Ltd.
Year first mentioned: 1986
Development status: Experimental
Chemical structure(s):
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Molecular weight: 408.41
Iso. SMILES: C[C@H]1[C@@]([C@H]([C@@H](O1)O[C@H]2[C@@H]([C@H]([C@@H]([C@H]([C@@H]2O)O)N=C(N)N)O)N=C(N)N)O)(CO)O
InChI Key: ACTKLUZDHCNOLG-IJJDTDNZSA-N
Can. SMILES: C[C@H]1[C@](CO)([C@H]([C@@H](O1)O[C@H]2[C@@H]([C@H]([C@@H]([C@H]([C@@H]2O)O)N=C(N)N)O)N=C(N)N)O)O
InChI: InChI=1S/C14H28N6O8/c1-3-14(26,2-21)10(25)11(27-3)28-9-5(20-13(17)18)6(22)4(19-12(15)16)7(23)8(9)24/h3-11,21-26H,2H2,1H3,(H4,15,16,19)(H4,17,18,20)/t3-,4-,5+,6-,7+,8-,9-,10-,11-,14+/m0/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/124201503
Citation: https://www.jstage.jst.go.jp/article/antibiotics1968/39/5/39_5_724/_article/-char/en

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