1.0 2026-09-23 00:03:46 UTC 2026-09-23 00:03:46 UTC FDB119147 Coprogen [(E)-5-[3-[(2S,5S)-5-[3-[[(E)-5-hydroxy-3-methylpent-2-enoyl]-oxidoamino]propyl]-3,6-dioxopiperazin-2-yl]propyl-oxidoamino]-3-methyl-5-oxopent-3-enyl] (2S)-2-acetamido-5-[[(E)-5-hydroxy-3-methylpent-2-enoyl]-oxidoamino]pentanoate;iron(3+) ferric [(E)-5-[3-[(2S,5S)-5-[3-[[(E)-5-hydroxy-3-methyl-pent-2-enoyl]-oxido-amino]propyl]-3,6-dioxo-piperazin-2-yl]propyl-oxido-amino]-3-methyl-5-oxo-pent-3-enyl] (2S)-2-acetamido-5-[[(E)-5-hydroxy-3-methyl-pent-2-enoyl]-oxido-amino]pentanoate C35H53FeN6O13 821.683 821.301997 iron(3+) ion N-[(2S)-1-{[(3E)-4-({3-[(2S,5S)-3,6-dihydroxy-5-{3-[(2E)-5-hydroxy-3-methyl-N-oxidopent-2-enamido]propyl}-2,5-dihydropyrazin-2-yl]propyl}(oxido)carbamoyl)-3-methylbut-3-en-1-yl]oxy}-5-[(2E)-5-hydroxy-3-methyl-N-oxidopent-2-enamido]-1-oxopentan-2-yl]ethanimidic acid iron(3+) ion N-[(2S)-1-{[(3E)-4-({3-[(2S,5S)-3,6-dihydroxy-5-{3-[(2E)-5-hydroxy-3-methyl-N-oxidopent-2-enamido]propyl}-2,5-dihydropyrazin-2-yl]propyl}(oxido)carbamoyl)-3-methylbut-3-en-1-yl]oxy}-5-[(2E)-5-hydroxy-3-methyl-N-oxidopent-2-enamido]-1-oxopentan-2-yl]ethanimidic acid [Fe+3].[H]\C(=C(\C)CCO)C(=O)N([O-])CCC[C@]([H])(N=C(C)O)C(=O)OCC\C(C)=C(/[H])C(=O)N([O-])CCC[C@]1([H])N=C(O)[C@]([H])(CCCN([O-])C(=O)C(\[H])=C(/C)CCO)N=C1O InChI=1S/C35H53N6O13.Fe/c1-23(11-17-42)20-30(45)39(51)14-5-8-27-33(48)38-28(34(49)37-27)9-6-15-40(52)32(47)22-25(3)13-19-54-35(50)29(36-26(4)44)10-7-16-41(53)31(46)21-24(2)12-18-43;/h20-22,27-29,42-43H,5-19H2,1-4H3,(H,36,44)(H,37,49)(H,38,48);/q-3;+3/b23-20+,24-21+,25-22+;/t27-,28-,29-;/m0./s1 FQIVLXIUJLOKPL-DWZMLRRXSA-N belongs to the class of organic compounds known as n-acyl-alpha amino acids and derivatives. N-acyl-alpha amino acids and derivatives are compounds containing an alpha amino acid (or a derivative thereof) which bears an acyl group at its terminal nitrogen atom. N-acyl-alpha amino acids and derivatives Organic compounds Organic acids and derivatives Carboxylic acids and derivatives Amino acids, peptides, and analogues Aliphatic heteromonocyclic compounds 2,5-dioxopiperazines Acetamides Alpha amino acid esters Azacyclic compounds Carbonyl compounds Carboxylic acid esters Fatty acid esters Hydrocarbon derivatives Lactams Monocarboxylic acids and derivatives Organic oxides Organic transition metal salts Organic zwitterions Organonitrogen compounds Organopnictogen compounds Primary alcohols Secondary carboxylic acid amides 1,4-diazinane 2,5-dioxopiperazine Acetamide Alcohol Aliphatic heteromonocyclic compound Alpha-amino acid ester Azacycle Carbonyl group Carboxamide group Carboxylic acid ester Dioxopiperazine Fatty acid ester Fatty acyl Hydrocarbon derivative Lactam Monocarboxylic acid or derivatives N-acyl-alpha amino acid or derivatives Organic nitrogen compound Organic oxide Organic oxygen compound Organic salt Organic transition metal salt Organic zwitterion Organoheterocyclic compound Organonitrogen compound Organooxygen compound Organopnictogen compound Piperazine Primary alcohol Secondary carboxylic acid amide logp 2.31 ALOGPS logs -4.51 ALOGPS solubility 2.85e-02 g/l ALOGPS logp -1.6 ChemAxon pka_strongest_acidic 4.14 ChemAxon pka_strongest_basic 2.2 ChemAxon iupac iron(3+) ion N-[(2S)-1-{[(3E)-4-({3-[(2S,5S)-3,6-dihydroxy-5-{3-[(2E)-5-hydroxy-3-methyl-N-oxidopent-2-enamido]propyl}-2,5-dihydropyrazin-2-yl]propyl}(oxido)carbamoyl)-3-methylbut-3-en-1-yl]oxy}-5-[(2E)-5-hydroxy-3-methyl-N-oxidopent-2-enamido]-1-oxopentan-2-yl]ethanimidic acid ChemAxon average_mass 821.683 ChemAxon mono_mass 821.301997 ChemAxon smiles [Fe+3].[H]\C(=C(\C)CCO)C(=O)N([O-])CCC[C@]([H])(N=C(C)O)C(=O)OCC\C(C)=C(/[H])C(=O)N([O-])CCC[C@]1([H])N=C(O)[C@]([H])(CCCN([O-])C(=O)C(\[H])=C(/C)CCO)N=C1O ChemAxon formula C35H53FeN6O13 ChemAxon inchi InChI=1S/C35H53N6O13.Fe/c1-23(11-17-42)20-30(45)39(51)14-5-8-27-33(48)38-28(34(49)37-27)9-6-15-40(52)32(47)22-25(3)13-19-54-35(50)29(36-26(4)44)10-7-16-41(53)31(46)21-24(2)12-18-43;/h20-22,27-29,42-43H,5-19H2,1-4H3,(H,36,44)(H,37,49)(H,38,48);/q-3;+3/b23-20+,24-21+,25-22+;/t27-,28-,29-;/m0./s1 ChemAxon inchikey FQIVLXIUJLOKPL-DWZMLRRXSA-N ChemAxon polar_surface_area 294.64 ChemAxon refractivity 194.4 ChemAxon polarizability 78.91 ChemAxon rotatable_bond_count 25 ChemAxon acceptor_count 15 ChemAxon donor_count 5 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon