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ChemicalBook--->CAS DataBase List--->15005-62-6

15005-62-6

15005-62-6 Structure

15005-62-6 Structure
IdentificationBack Directory
[Name]

bottromycin A(2)
[CAS]

15005-62-6
[Synonyms]

bottromycin A(2)
b-Alanine, N-[(2S)-2-[[glycyl-(3R)-3-methyl-Lprolyl-L-valyl]amino]-1-imino-3,3-dimethylbutyl]-3-methyl-L-valyl-(bS)-b-methyl-L-phenylalanyl-3-(2-thiazolyl)-, methyl ester, cyclic (1')-imine,(3R)-
β-Alanine, N-[(2S)-2-[[glycyl-(3R)-3-methyl-L-prolyl-L-valyl]amino]-1-imino-3,3-dimethylbutyl]-3-methyl-L-valyl-(βS)-β-methyl-L-phenylalanyl-3-(2-thiazolyl)-, methyl ester, cyclic (1→1')-imine, (3R)-
[Molecular Formula]

C42H62N8O7S
[MDL Number]

MFCD34166124
[MOL File]

15005-62-6.mol
[Molecular Weight]

823.07
Chemical PropertiesBack Directory
[Boiling point ]

1061.3±65.0 °C(Predicted)
[density ]

1.28±0.1 g/cm3(Predicted)
[storage temp. ]

-20°C
[solubility ]

Ether: soluble,Methanol: soluble,
[form ]

A solid
[pka]

12.18±0.46(Predicted)
[Water Solubility ]

Water: soluble
Hazard InformationBack Directory
[Uses]

Bottromycin A2 is a natural antibiotic. Bottromycin A2 is active against methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant Enterococci (VRE)[1].
[Biological Activity]

Bottromycin A2 is an antibiotic originally isolated from Streptomyces.1 It blocks the binding of aminoacyl-tRNA to the A site of the 50S ribosome, inhibiting protein synthesis.2 Bottromycin A2 is active against clinical isolates of methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant Enterococci with MIC values of 1 and 0.5 μg/ml, respectively.
[References]

1.Nakamura, S., Yajima, T., Lin, Y., et al.Isolation and characterization of bottromycins A2, B2, C2J. Antibiot. (Tokyo)20(1)1-5(1967) 2.Gouda, H., Kobayashi, Y., Yamada, T., et al.Three-dimensional solution structure of bottromycin A2: A potent antibiotic active against methicillin-resistant Staphylococcus aureus and vancomycin-resistant EnterococciChem. Pharm. Bull. (Tokyo)60(2)169-171(2012)
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