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CAS 13058-67-8

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Lucensomycin

Description:
Lucensomycin is a naturally occurring antibiotic that belongs to the class of compounds known as aminoglycosides. It is produced by certain strains of the bacterium *Micromonospora* and exhibits antibacterial properties primarily against Gram-positive bacteria. The chemical structure of lucensomycin features a complex arrangement of sugar moieties and an amino group, which contribute to its biological activity. This compound functions by inhibiting protein synthesis in bacteria, thereby preventing their growth and replication. Lucensomycin has garnered interest in pharmaceutical research due to its potential therapeutic applications, particularly in treating infections caused by resistant bacterial strains. Its unique mechanism of action and structural characteristics make it a subject of study for developing new antibiotics. However, like many antibiotics, the emergence of resistance poses challenges to its clinical use, necessitating ongoing research to understand its efficacy and safety profile in various medical contexts.
Formula:C36H53NO13
InChI:InChI=1S/C36H53NO13/c1-3-4-12-23-13-10-8-6-5-7-9-11-14-24(48-35-33(42)31(37)32(41)21(2)46-35)18-28-30(34(43)44)25(39)20-36(45,50-28)19-22(38)17-27-26(49-27)15-16-29(40)47-23/h5-11,14-16,21-28,30-33,35,38-39,41-42,45H,3-4,12-13,17-20,37H2,1-2H3,(H,43,44)/b6-5+,9-7+,10-8+,14-11+,16-15+/t21-,22+,23?,24+,25+,26-,27-,28+,30-,31+,32-,33+,35+,36-/m1/s1
InChI key:InChIKey=MUAOHYJGHYFDSA-YZMLMZOASA-N
SMILES:C(O)(=O)[C@H]1[C@]2(O[C@@](O)(C[C@@H]1O)C[C@@H](O)C[C@@]3([C@](O3)(/C=C/C(=O)OC(CCCC)C\C=C\C=C\C=C\C=C\[C@H](O[C@H]4[C@@H](O)[C@@H](N)[C@H](O)[C@@H](C)O4)C2)[H])[H])[H]
Synonyms:
  • (1R,3S,5R,7R,8E,14E,16E,18E,20E,22R,24S,25R,26S)-22-[(3-Amino-3,6-dideoxy-β-<span class="text-smallcaps">D</span>-mannopyranosyl)oxy]-12-butyl-1,3,26-trihydroxy-10-oxo-6,11,28-trioxatricyclo[22.3.1.0<sup>5,7</sup>]octacosa-8,14,16,18,20-pentaene-25-carboxylic acid
  • (8E)-22-[(3-amino-3,6-dideoxy-beta-D-glycero-hexopyranosyl)oxy]-12-butyl-1,3,26-trihydroxy-10-oxo-6,11,28-trioxatricyclo[22.3.1.0~5,7~]octacosa-8,14,16,18,20-pentaene-25-carboxylic acid
  • 6,11,28-Trioxatricyclo(22.3.1.05,7)octacowq-8,14,16,18,20-pentaene-25-carboxylic acid, 22-((3-amino-3,6-dideoxy-beta-D-mannopyranosyl)oxy)-12-butyl-1,3,26-trihydroxy-10-oxo-
  • 6,11,28-Trioxatricyclo[22.3.1.0<sup>5,7</sup>]octacosa-8,14,16,18,20-pentaene-25-carboxylic acid, 22-[(3-amino-3,6-dideoxy-β-<span class="text-smallcaps">D</span>-mannopyranosyl)oxy]-12-butyl-1,3,26-trihydroxy-10-oxo-
  • 6,11,28-Trioxatricyclo[22.3.1.0<sup>5,7</sup>]octacosane, lucensomycin deriv.
  • Antibiotic 1163 F.I.
  • Antibiotic FI 1163
  • Antibiotic obtained from cultures of Streptomyces lucensis, or the same substance produced by any other means
  • Etruscomicina
  • Etruscomycin
  • See more synonyms
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Found 2 products.
  • Lucimycin
    Targetmol
    + Info

    Lucimycin

    CAS:
    Lucimycin is a macrolide antibiotic from cultures of Streptomyces lucensis.
    Formula:C36H53NO13
    Color and Shape:Solid
    Molecular weight:707.814

    Ref: TM-T25762

  • Lucimycin
    Biosynth
    + Info

    Lucimycin

    CAS:
    <p>Lucimycin is an antibiotic, which is derived from the fermentation of specific Streptomyces bacterial strains. This compound exerts its antibacterial effects by binding to the 50S subunit of the bacterial ribosome, thereby inhibiting protein synthesis and effectively halting bacterial growth. Lucimycin is particularly effective against Gram-positive bacteria and some Gram-negative species, making it a valuable tool in both clinical and research settings.</p>
    Formula:C36H53NO13
    Purity:Min. 95%
    Molecular weight:707.8 g/mol

    Ref: 3D-FL177686

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