Page last updated: 2024-08-05 11:27:49

indolecarboxamide

null

ChEBI ID: 46921

Members (28)

MemberDefinitionRole
1-(2-Naphthylmethyl)-2,3-dioxo-indoline-5-carboxamide1-(2-Naphthylmethyl)-2,3-dioxo-indoline-5-carboxamide
1-[(1R)-1-(1-ethylsulfonyl-4-piperidinyl)ethyl]-N-[(4-methoxy-6-methyl-2-oxo-1H-pyridin-3-yl)methyl]-2-methyl-3-indolecarboxamide1-[(1R)-1-(1-ethylsulfonyl-4-piperidinyl)ethyl]-N-[(4-methoxy-6-methyl-2-oxo-1H-pyridin-3-yl)methyl]-2-methyl-3-indolecarboxamide
1-[1-naphthalenyl(oxo)methyl]-3-indolecarboxylic acid methyl ester1-[1-naphthalenyl(oxo)methyl]-3-indolecarboxylic acid methyl ester
1-[2-(dimethylamino)ethyl]-5-methoxy-N-methyl-2-indolecarboxamide1-[2-(dimethylamino)ethyl]-5-methoxy-N-methyl-2-indolecarboxamide
3-amino-4-methoxy-1H-indole-2-carbohydrazide3-amino-4-methoxy-1H-indole-2-carbohydrazide
3-fluoro-Nalpha-(1H-indol-2-ylcarbonyl)-N-{(2S)-1-oxo-3-[(3S)-2-oxopyrrolidin-3-yl]propan-2-yl}-L-phenylalaninamideA secondary carboxamide resulting from the formal condensation of the carboxy group of 1H-indole-2-carboxylic acid with the primary amino group of 3-fluoro-N-{(2S)-1-oxo-3-[(3S)-2-oxopyrrolidin-3-yl]propan-2-yl}-L-phenylalaninamide. It is an inhibitor of SARS coronavirus main proteinase and inhibits SARS-CoV-2 replication in cell culture (EC50 = 0.72 muM).3-fluoro-Nalpha-(1H-indol-2-ylcarbonyl)-N-{(2S)-1-oxo-3-[(3S)-2-oxopyrrolidin-3-yl]propan-2-yl}-L-phenylalaninamide
5-methoxy-N-(1-methoxypropan-2-yl)-1H-indole-2-carboxamide5-methoxy-N-(1-methoxypropan-2-yl)-1H-indole-2-carboxamide
AM2201AM2201
delavirdineThe amide resulting from the formal condensation of 5-[(methylsulfonyl)amino]-1H-indole-2-carboxylic acid and 4-amino group of 1-[3-(isopropylamino)pyridin-2-yl]piperazine, delavirdine is a non-nucleoside reverse transcriptase inhibitor with activity specific for HIV-1. Viral resistance emerges rapidly when delavirdine is used alone, so it is therefore used (as the methanesulfonic acid salt) with other antiretrovirals for combination therapy of HIV infection.delavirdine
devazepideAn indolecarboxamide obtained by formal condensation of the carboxy group of indole-2-carboxylic acid with the exocyclic amino group of (3S)-3-amino-1-methyl-5-phenyl-1,3-dihydro-1,4-benzodiazepin-2-one. A cholecystokinin antagonist used for treatment of gastrointestinal disorders.devazepide
jaw1H-indole-5-carboxamide
jhw 015(2-methyl-1-propyl-3-indolyl)-(1-naphthalenyl)methanone
jwh 018JWH 018
jwh-0731-Butyl-3-(1-naphthoyl)indole
jwh-210JWH182
N-[(2S)-3-cyclohexyl-1-oxo-1-({(2S)-1-oxo-3-[(3S)-2-oxopyrrolidin-3-yl]propan-2-yl}amino)propan-2-yl]-1H-indole-2-carboxamideA secondary carboxamide resulting from the formal condensation of the carboxy group of 1H-indole-2-carboxylic acid with the primary amino group of 3-cyclohexyl-N-{(2S)-1-oxo-3-[(3S)-2-oxopyrrolidin-3-yl]propan-2-yl}-L-alaninamide. It is an inhibitor of SARS coronavirus main proteinase and inhibits SARS-CoV-2 replication in cell culture (EC50 = 0.53 muM).N-[(2S)-3-cyclohexyl-1-oxo-1-({(2S)-1-oxo-3-[(3S)-2-oxopyrrolidin-3-yl]propan-2-yl}amino)propan-2-yl]-1H-indole-2-carboxamide
N-[[1H-indol-2-yl(oxo)methyl]amino]carbamic acid (phenylmethyl) esterN-[[1H-indol-2-yl(oxo)methyl]amino]carbamic acid (phenylmethyl) ester
N-butyl-5-methoxy-1H-indole-2-carboxamideN-butyl-5-methoxy-1H-indole-2-carboxamide
n,n-dipropylcarboxamidotryptamine3-[2-(dipropylamino)ethyl]-1H-indole-5-carboxamide
N'-[(2-chlorophenyl)-oxomethyl]-5-(trifluoromethoxy)-1H-indole-2-carbohydrazideN'-[(2-chlorophenyl)-oxomethyl]-5-(trifluoromethoxy)-1H-indole-2-carbohydrazide
nsc 716970An indolecarboxamide obtained by the formal condensation of the carboxy group of 5,6,7-trimethoxyindole-2-carboxylic acid with the 2-amino group of 1-(2-chloroethyl)-2,4-diaminonaphthalene.AS-I-145
pci 34051N-hydroxy-1-[(4-methoxyphenyl)methyl]-6-indolecarboxamide
PF-00835231A primary alcohol resulting from the cleavage of the phosphate group of the prodrug PF-07304814. It is an inhibitor of SARS-CoV-1 and -2 main protease (3CLpro) and exhibits potent in vitro antiviral activity.PF-00835231
PF-07304814An indolecarboxamide resulting from the formal condensation of the carboxy group of 4-methoxy-1H-indole-2-carboxylic acid with the primary amino group of N-[(2S)-3-oxo-1-[(3S)-2-oxopyrrolidin-3-yl]-4-(phosphonooxy)butan-2-yl]-L-leucinamide. It is the phosphate prodrug of PF-00835231, an anticoronaviral agent.PF-07304814
scio-469An indolecarboxamide obtained by formal condensation of the carboxy group of 6-chloro-3-[(dimethylamino)(oxo)acetyl]-1-methylindole-5-carboxylic acid with the secondary amino group of (2S,5R)-1-[(4-fluorophenyl)methyl]-2,5-dimethylpiperazine. It is a potent inhibitor of MAPK and exhibits anti-cancer properties.talmapimod
silodosinsilodosin
sr1664[1,1'-biphenyl]-2-carboxylic acid, 4'-[[2,3-dimethyl-5-[[[(1s)-1-(4-nitrophenyl)ethyl]amino]carbonyl]-1h-indol-1-yl]methyl]-
sts-135STS-135

Research

Studies (8,688)

TimeframeStudies, Drugs in This Class (%)All Drugs %
pre-19902,891 (33.28)18.7374
1990's1,391 (16.01)18.2507
2000's1,627 (18.73)29.6817
2010's2,157 (24.83)24.3611
2020's622 (7.16)2.80

Study Types

Publication TypeStudies, Drugs in This Class (%)All Drugs (%)
Trials275 (2.88%)5.53%
Reviews650 (6.81%)6.00%
Case Studies477 (5.00%)4.05%
Observational24 (0.25%)0.25%
Other8,121 (85.06%)84.16%