ChemicalBook--->CAS DataBase List--->38129-37-2

38129-37-2

38129-37-2 Structure

38129-37-2 Structure
IdentificationBack Directory
[Name]

bicozamycin
[CAS]

38129-37-2
[Synonyms]

C11259
WS-4545
ICOZAMYCIN
bicozamycin
BicycloMycin
BicozaMycin benzoate
BicozaMycin, AizuMycin, Bacteron, CGP 3543E, WS4545, 5879
(1R,6S)-1-hydroxy-2-methylidene-6-[(1S,2S)-1,2,3-trihydroxy-2-methylpropyl]-5-oxa-8,10-diazabicyclo[4.2.2]decane-7,9-dione
2-Oxa-7,9-diazabicyclo[4.2.2]decane-8,10-dione, 6-hydroxy-5-methylene-1-[(1S,2S)-1,2,3-trihydroxy-2-methylpropyl]-, (1S,6R)-
[EINECS(EC#)]

253-795-3
[Molecular Formula]

C12H18N2O7
[MOL File]

38129-37-2.mol
[Molecular Weight]

302.28
Chemical PropertiesBack Directory
[Melting point ]

188-191° (dec); mp 187-189° (dec) (Imanaka); mp 166-170° (Nakatsuka et al.)
[alpha ]

D23 +63.5° (methanol)
Safety DataBack Directory
[Symbol(GHS) ]

Skull and Crossbones (GHS06)
GHS06
[Signal word ]

Danger
[Hazard statements ]

H300
[Precautionary statements ]

P264-P270-P301+P310-P321-P330-P405-P501
[Toxicity]

LD50 in mice: >4 g/kg (Williams, Durham)
Hazard InformationBack Directory
[Uses]

Bicyclomycin is a polar metabolite first isolated from Streptomyces sapporonensis in 1972. The selective Gram negative profile of bicyclomycin is rare among Streptomyces metabolites. The primary site of action for bicyclomycin is thought to be the rho transcription termination factor.
[Definition]

ChEBI: A commercially important azabicyclic antibiotic obtained from Streptomyces sapporonensis. It inhibits the Rho protein of E. coli.
Spectrum DetailBack Directory
[Spectrum Detail]

bicozamycin(38129-37-2)MS
bicozamycin(38129-37-2)IR1
bicozamycin(38129-37-2)IR2
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