Compound ID | 3215

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KA-5685

Synonym(s): KA 5685  |  KA5685

Class: Aminoglycoside

Agent Type: Natural product; Small molecule; Direct acting;
Spectrum of activity: Gram-positive & Gram-negative
Mechanism of action: Protein synthesis inhibitor
Target Pathogen: Active against Staphylococcus aureus, Streptococcus faecalis, Escherichia coli (including strains expressing AAC(3)-IV), Klebsiella pneumoniae, and Pseudomonas aeruginosa
Description: Natural product from Saccharopolyspora hirsuta
Institute where first reported: Tokyo Research Laboratories, Kowa Co., Ltd.
Year first mentioned: 1983
Development status: Experimental
Chemical structure(s):
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Molecular weight: 541.55
Iso. SMILES: CN[C@H]1[C@H]([C@@H]2[C@H](C[C@H]([C@H](O2)O[C@@H]3[C@H](C[C@H]([C@@H]([C@H]3O)O)N)O)N)O[C@@H]1O[C@@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)O
InChI Key: CANJCXYUUJPQSP-OKXNOFASSA-N
Can. SMILES: CN[C@H]1[C@H]([C@@H]2[C@H](C[C@H]([C@@H](O[C@@H]3[C@H](C[C@H]([C@@H]([C@H]3O)O)N)O)O2)N)O[C@@H]1O[C@@H]4[C@@H]([C@H]([C@@H]([C@@H](CO)O4)O)O)O)O
InChI: InChI=1S/C21H39N3O13/c1-24-10-13(29)18-8(33-20(10)37-21-16(32)14(30)12(28)9(4-25)34-21)3-6(23)19(36-18)35-17-7(26)2-5(22)11(27)15(17)31/h5-21,24-32H,2-4,22-23H2,1H3/t5-,6-,7+,8+,9-,10+,11+,12-,13-,14+,15-,16-,17-,18+,19+,20-,21-/m1/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/3086226
Citation: https://www.jstage.jst.go.jp/article/antibiotics1968/36/6/36_6_738/_article/-char/en

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