Page last updated: 2024-08-05 10:53:32

dicarboxylic acid monoamide

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ChEBI ID: 35735

Members (18)

MemberDefinitionRole
2-(4-(2-carboxyethyl)phenethylamino)-5'-n-ethylcarboxamidoadenosineA derivative of adenosine in which the 5'-hydroxymethyl group is replaced by N-ethylcarboxamido and the hydrogen at position 2 on the adenine is replaced by a 4-(2-carboxyethyl)phenethylamino group.CGS-21680
alpha-naphthylphthalamic acidA dicarboxylic acid monoamide which results from addition of one equivalent of 1-naphthylamine to phthalic anhydride.naptalam
cathestatin bA carboxamide obtained by the formal condensation of the carboxylic group of oxirane-2,3-dicarboxylic acid with the amino group of N-(4-aminobutyl)-L-tyrosinamide (the 2S,3S stereoisomer). An antibiotic isolated from the fermentation broth of Penicillium citrinum, it acts as a potent inhibitor of cysteine protease.cathestatin B
coprineA non-proteinogenic L-alpha-amino acid that is L-glutamine in which one of the hydrogens attached to the amide nitrogen is replaced by a 1-hydroxycyclopropyl group. Found in the ink-cap mushroom, Coprinus atramentarius, it causes an unpleasant hypersensitivity to alcohol (the 'disulfiram effect').coprine
e 64E64 zwitterion; E64
EG00229A member of the class of thiophenes that is thiophene substituted by a carbonyl-L-arginine and (2,1,3-benzothiadiazole-4-sulfonyl)amino groups at positions 2 and 3. It is an inhibitor of the neuropilin-1 and VEGF-A interaction and a potential anti-cancer agent.EG00229
fumimycinA member of the class of 1-benzofurans that is 1-benzofuran-2(3H)-one substituted by a propenyl group at position 4, hydroxy groups at positions 5 and 6, methyl group at position 3 and a [(2E)-3-carboxyprop-2-enoyl]nitrilo group at position 3. Isolated from the fermentation broth of Aspergillus fumisynnematus F746, it exhibits antibacterial activity.fumimycin
ioxitalamic acidAn organoiodine compound that is 2,4,6-triiodobenzoic acid substituted by an acetylamino group at position 3 and a (2-hydroxyethyl)carbamoyl group at position 5. It is used as a contrast medium.iooxitalamic acid
lorglumideA dicarboxylic acid monoamide obtained by formal condensation of the alpha-carboxy group of N-(3,4-dichlorobenzoyl)glutamic acid with the amino group of dipentylamine.N(2)-(3,4-dichlorobenzoyl)-N,N-dipentyl-alpha-glutamine
maleamic acidA dicarboxylic acid monoamide of maleamic acid.maleamic acid
mannopineA hexitol derivative that is D-mannitol in which the hydroxy group at position 1 is replaced by the alpha-amino group of L-glutamine. It is produced in crown gall tumours induced in a wide range of dicotyledenous plants by Agrobacterium tumefaciens.mannopine
melagatranA member of the class of azetidines that is (2S)-azetidine 2-carboxylic acid in which the carboxylic acid has been converted to the amide corresponding to formal condensation with 4-(aminomethyl)benzenecarboximidamide and in which the hydrogen attached to the azetidine nitrogen is replaced by a (2R)-2-cyclohexyl-2-[(carboxymethyl)amino]acetyl group.melagatran
N-malonylanthranilic acidN-malonylanthranilic acid
oxamic acidA dicarboxylic acid monoamide resulting from the formal condensation of one of the carboxy groups of oxalic acid with ammonia.oxamic acid
phthalylsulfathiazoleA sulfonamide incorporating 2-carboxybenzamido and 1,3-thiazol-2-yl moieties that is a broad-spectrum antibiotic indicated in the treatment of dysentery, colitis, gastroenteritis and intestinal surgery.phthalylsulfathiazole
proglumideA dicarboxylic acid monoamide obtained by formal condensation of the alpha-carboxy group of N-benzoylglutamic acid with dippropylamine.N(2)-benzoyl-N,N-dipropyl-alpha-glutamine; proglumide
tamibaroteneA dicarboxylic acid monoamide resulting from the condensation of one of the carboxy groups of terephthalic acid with the amino group of 5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-amine.tamibarotene
varespladibA member of the class of indoles that is 1H-indole substituted by benzyl, ethyl, oxamoyl, and carboxymethoxy groups at positions 1, 2, 3, and 4, respectively. It is an oral secretory phospholipase A2 inhibitor and exhibits anti-inflammatory effects.varespladib

Research

Studies (3,602)

TimeframeStudies, Drugs in This Class (%)All Drugs %
pre-1990670 (18.60)18.7374
1990's1,082 (30.04)18.2507
2000's1,025 (28.46)29.6817
2010's706 (19.60)24.3611
2020's119 (3.30)2.80

Study Types

Publication TypeStudies, Drugs in This Class (%)All Drugs (%)
Trials213 (5.32%)5.53%
Reviews137 (3.42%)6.00%
Case Studies33 (0.82%)4.05%
Observational0 (0.00%)0.25%
Other3,624 (90.44%)84.16%