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0007564038
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Micrococcin. An antibacterial substance formed by a strain of Micrococcus
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A new antibiotic of bacterial origin
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The macrocyclic peptide antibiotic micrococcin P(1) is secreted by the food-borne bacterium Staphylococcus equorum WS2733 and inhibits Listeria monocytogenes on soft cheese
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The antibiotic micrococcin is a potent inhibitor of growth and protein synthesis in the malaria parasite
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Antibiotics micrococcin and thiostrepton interact directly with 23S rRNA nucleotides 1067A and 1095A
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The antibiotic micrococcin acts on protein L11 at the ribosomal GTPase centre
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Synthesis of the Bycroft-Gowland structure of micrococcin P1
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Chemistry of micrococcin P. Part II
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Chemistry of micrococcin P. Part VI. Racemisation of 2-(1-amino-2- methylpropyl)thiazole-4-carboxylic acid, and related studies
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DEAN, B. M.; M. P. V. MIJOVIC & J. WALKER: Chemistry of micrococcin P. Part VI. Racemisation of 2-(1-amino-2-methylpropyl)thiazole-4-carboxylic acid, and related studies. J. Chem. Soc.: 3394-3400, 1961
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Dean, B.M.1
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17
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84973069306
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The chiral synthesis of thiazole amino acid enantiomers
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0042659297
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Concise synthesis of stereodefined, thiazole-containing cyclic hexa- and octapeptide relatives of the Lissoclinums, via cyclooligomerisation reactions
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BERTRAM, A.; A. J. BLAKE, F. GONZALEZ-LOPEZ DE TURISO, J. S. HANNAM, K. A. JOLLIFFE, G. PATTENDEN & M. SKAE: Concise synthesis of stereodefined, thiazole-containing cyclic hexa- and octapeptide relatives of the Lissoclinums, via cyclooligomerisation reactions. Tetrahedron 59: 6979-6990, 2003
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19
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0028211499
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Reinvestigation of a modified Hantzsch thiazole synthesis
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AGUILAR, E. & A. I. MEYERS: Reinvestigation of a modified Hantzsch thiazole synthesis. Tetrahedron Lett. 35: 2473-2476, 1994
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Aguilar, E.1
Meyers, A.I.2
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20
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85039481575
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note
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2O and so must be analysed immediately following isolation.
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21
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37049049443
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Chemistry of micrococcin P. Part I
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The original specific rotation of thiazole 8 isolated from micrococcin was erroneously reported as dextrorotatory. BROOKES, P.; A. T. FULLER & J. WALKER: Chemistry of micrococcin P. Part I. J. Chem. Soc.: 689-699, 1957. This was corrected subsequently.16) In three separate hydrolysis experiments, the specific rotation was found to be laevorotatory at concentrations ranging from c 0.5-2.5.
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J. Chem. Soc.
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Brookes, P.1
Fuller, A.T.2
Walker, J.3
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