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| | (7S)-7-[[(R)-5-Amino-5-carboxy-1-oxopentyl]amino]-7-methoxy-3-[[[6-amino-3-hydroxy-4-(L-ornithyl-L-valyl-L-ornithyl-L-valylamino)-1,6-dioxohexyl]oxy]methyl]cepham-3-ene-4-carboxylic acid Basic information |
| | (7S)-7-[[(R)-5-Amino-5-carboxy-1-oxopentyl]amino]-7-methoxy-3-[[[6-amino-3-hydroxy-4-(L-ornithyl-L-valyl-L-ornithyl-L-valylamino)-1,6-dioxohexyl]oxy]methyl]cepham-3-ene-4-carboxylic acid Chemical Properties |
| Boiling point | 1407.087±65.00 °C(Press: 760.00 Torr)(predicted) | | density | 1.409±0.10 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted) | | pka | 2.494±0.24(predicted) | | Sequence | {Orn}-Val-{Orn}-Val-{Oaa} |
| | (7S)-7-[[(R)-5-Amino-5-carboxy-1-oxopentyl]amino]-7-methoxy-3-[[[6-amino-3-hydroxy-4-(L-ornithyl-L-valyl-L-ornithyl-L-valylamino)-1,6-dioxohexyl]oxy]methyl]cepham-3-ene-4-carboxylic acid Usage And Synthesis |
| Description | Cephabacin M4 is a new cephem antibiotics of bacterial origin. | | Uses | Cephabacin M4 is a cephalosporin component, a 7-methoxydesacetylcephalosporin. Cephabacin M4 can be isolated from the culture filtrate of Xanthomonas lactamica. | | References | [1] NOZAKI Y, KATAYAMA N, TSUBOTANI S, et al. CEPHABACIN M1-6, NEW 7-METHOXYCEPHEM ANTIBIOTICS OF BACTERIAL ORIGIN I. A PRODUCING ORGANISM, FERMENTATION, BIOLOGICAL ACTIVITIES, AND MODE OF ACTION[J]. The Journal of Antibiotics, 1985, 38(9): 1141-1151. |
| | (7S)-7-[[(R)-5-Amino-5-carboxy-1-oxopentyl]amino]-7-methoxy-3-[[[6-amino-3-hydroxy-4-(L-ornithyl-L-valyl-L-ornithyl-L-valylamino)-1,6-dioxohexyl]oxy]methyl]cepham-3-ene-4-carboxylic acid Preparation Products And Raw materials |
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