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| | L-Ornithine, N2-acetyl-N5-hydroxy-N5-[(2E)-5-hydroxy-3-methyl-1-oxo-2-penten-1-yl]-, (3E)-5-[hydroxy[3-[(2S,5S)-5-[3-[hydroxy[(2E)-5-hydroxy-3-methyl-1-oxo-2-penten-1-yl]amino]propyl]-3,6-dioxo-2-piperazinyl]propyl]amino]-3-methyl-5-oxo-3-penten-1-yl ester Basic information |
| | L-Ornithine, N2-acetyl-N5-hydroxy-N5-[(2E)-5-hydroxy-3-methyl-1-oxo-2-penten-1-yl]-, (3E)-5-[hydroxy[3-[(2S,5S)-5-[3-[hydroxy[(2E)-5-hydroxy-3-methyl-1-oxo-2-penten-1-yl]amino]propyl]-3,6-dioxo-2-piperazinyl]propyl]amino]-3-methyl-5-oxo-3-penten-1-yl ester Chemical Properties |
| density | 1.274±0.06 g/cm3(Predicted) | | pka | 8.76±0.50(Predicted) |
| | L-Ornithine, N2-acetyl-N5-hydroxy-N5-[(2E)-5-hydroxy-3-methyl-1-oxo-2-penten-1-yl]-, (3E)-5-[hydroxy[3-[(2S,5S)-5-[3-[hydroxy[(2E)-5-hydroxy-3-methyl-1-oxo-2-penten-1-yl]amino]propyl]-3,6-dioxo-2-piperazinyl]propyl]amino]-3-methyl-5-oxo-3-penten-1-yl ester Usage And Synthesis |
| Definition | ChEBI: Desferricoprogen is a member of the class of 2,5-diketopiperazines that is 2,5-diketopiperazine which is substituted at positions 3 and 6 by 3-(hydroxyamino)propyl groups in which the nitrogens have been acylated by (2E)-5-hydroxy-3-methylpent-2-enoyl groups. The substituent at position 3 has been further modified by having its terminal hydroxy group esterified by condensation with the carboxy group of N(2)-acetyl-N(5)-hydroxy-L-ornithine in which the N(5) nitrogen has been acylated by a (2E)-5-hydroxy-3-methylpent-2-enoyl group. It has a role as a siderophore. It is a hydroxamic acid, a carboxylic ester, a primary alcohol, a member of acetamides, a member of 2,5-diketopiperazines and a homoallylic alcohol. It is a conjugate acid of a desferricoprogen(3-). |
| | L-Ornithine, N2-acetyl-N5-hydroxy-N5-[(2E)-5-hydroxy-3-methyl-1-oxo-2-penten-1-yl]-, (3E)-5-[hydroxy[3-[(2S,5S)-5-[3-[hydroxy[(2E)-5-hydroxy-3-methyl-1-oxo-2-penten-1-yl]amino]propyl]-3,6-dioxo-2-piperazinyl]propyl]amino]-3-methyl-5-oxo-3-penten-1-yl ester Preparation Products And Raw materials |
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