Ketomycin
Code | Size | Price |
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TAR-T25574-5mg | 5mg | £850.00 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Overview
Regulatory Status: RUO
Shipping:
cool pack
Storage:
-20℃
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Further Information
Bioactivity:
Ketomycin is an antibiotic agent. It is formed from shikimic acid via chorismic acid and prephenic acid.
CAS:
23364-22-9
Formula:
C8H10O3
Molecular Weight:
154.165
Purity:
0.98
SMILES:
OC(=O)C(=O)[C@@H]1CCC=CC1
References
1. Takeda Y, Mak V, Chang CC, Chang CJ, Floss HG. Biosynthesis of ketomycin. J Antibiot (Tokyo). 1984 Aug;37(8):868-75. PubMed PMID: 6384167.
2. Jackson JH, Umbarger HE. Defective transamination, a mechanism for resistance to ketomycin in Escherichia coli. Antimicrob Agents Chemother. 1973 Apr;3(4):510-6. PubMed PMID: 4597727; PubMed Central PMCID: PMC444444.
3. Keller-Schierlein W, Poralla K, Z?hner H. [Metabolic products of microorganisms. 78. Isolation, identification and mechanism of action of ketomycin ((R)-3-cyclohexeneglyoxylic acid) and of the conversion product 3-cyclohexeneglycine]. Arch Mikrobiol. 1969;67(4):339-56. German. PubMed PMID: 4985531.
4. Kr?pe H, Poralla K. [Properties of mutants of Bacillus subtilis which are resistant to the isoleucine antagonist ketomycin]. Arch Mikrobiol. 1972;85(3):253-8. German. PubMed PMID: 4629239.