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93522-10-2

93522-10-2 Structure

93522-10-2 Structure
IdentificationBack Directory
[Name]

(2E,4E,6E)-7-[3-hydroxy-5-[(4E,6E)-3-methoxy-4-methyl-8-[2-[2,4,5-trih ydroxy-5-methyl-6-[(1E,3E)-penta-1,3-dienyl]oxan-2-yl]butanoylamino]oc ta-4,6-dien-2-yl]oxolan-2-yl]hepta-2,4,6-trienoic acid
[CAS]

93522-10-2
[Synonyms]

L681
L-681
L 681
L 681217
(2E,4E,6E)-7-[3-hydroxy-5-[(4E,6E)-3-methoxy-4-methyl-8-[2-[2,4,5-trih ydroxy-5-methyl-6-[(1E,3E)-penta-1,3-dienyl]oxan-2-yl]butanoylamino]oc ta-4,6-dien-2-yl]oxolan-2-yl]hepta-2,4,6-trienoic acid
2,4,6-Heptatrienoic acid, 7-[tetrahydro-3-hydroxy-5-[2-methoxy-1,3-dimethyl-7-[[1-oxo-2-[tetrahydro-2,4,5-trihydroxy-5-methyl-6-(1,3-pentadien-1-yl)-2H-pyran-2-yl]butyl]amino]-3,5-heptadien-1-yl]-2-furanyl]-
[Molecular Formula]

C36H53NO10
[MDL Number]

MFCD09752705
[MOL File]

93522-10-2.mol
[Molecular Weight]

659.812
Chemical PropertiesBack Directory
[solubility ]

DMF: soluble
DMSO: soluble
Ethanol: soluble
Methanol: soluble
Hazard InformationBack Directory
[Uses]

L 681,217 is a glycolipid-type antibiotic related to the efrotomycin class, isolated from a Streptomyces sp.. L 681,217 also shows broad spectrum antibiotic activity against Gram positive and Gram negative bacteria. L-681,217 inhibits bacterial protein synthesis at the elongation stage, its target being elongation factor Tu (EF-Tu).
[Uses]

L-681,217 is a glycolipid-type antibiotic related to the efrotomycin class, isolated from a Streptomyces sp.. L 681,217 shows broad spectrum antibiotic activity against Gram positive and Gram negative bacteria. L-681,217 inhibits bacterial protein synthesis at the elongation stage, its target being elongation factor Tu (EF-Tu).
[References]

[1] A J KEMPF. L-681,217, a new and novel member of the efrotomycin family of antibiotics.[J]. Journal of Antibiotics, 1986, 39 10: 1361-1367. DOI: 10.7164/antibiotics.39.1361
[2] C C HALL  N H G  J D Watkins. Effects of elfamycins on elongation factor Tu from Escherichia coli and Staphylococcus aureus.[J]. Antimicrobial Agents and Chemotherapy, 1989, 33 3: 322-325. DOI: 10.1128/aac.33.3.322
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