Page last updated: 2024-12-04

indoleacetamide

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

indoleacetamide: article does not mention position of acetamide group; amide of indole-3-acetic acid (IAA), the natural auxin found in plants [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

indole-3-acetamide : A member of the class of indoles that is acetamide substituted by a 1H-indol-3-yl group at position 2. It is an intermediate in the production of plant hormone indole acetic acid (IAA). [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID397
CHEBI ID16031
SCHEMBL ID40822
SCHEMBL ID8082815
MeSH IDM0065613

Synonyms (65)

Synonym
AKOS001129741
nsc1969
nsc-1969
CHEBI:16031
TSR ,
3-indoleacetamide
2-(3-indolyl)acetamide
3-indolylacetamide
nsc 1969
indole-3-acetamide (6ci,8ci)
(indol-3-yl)acetamide
indole-3-acetamide
2-(1h-indol-3-yl)acetamide
879-37-8
indoleacetamide
C02693
1h-indole-3-acetamide
indole-3-acetamide, 98%
c10h10n2o
OPREA1_704903
I-0900
99FEA035-A073-4863-9F14-923310E3BC45
DB08652
BMSE000696
zoambxdogprzlp-uhfffaoysa-
inchi=1/c10h10n2o/c11-10(13)5-7-6-12-9-4-2-1-3-8(7)9/h1-4,6,12h,5h2,(h2,11,13)
I0668
HMS1740A02
auxin amide
o9sew65xw3 ,
einecs 212-904-4
unii-o9sew65xw3
FT-0615869
FS-2701
AM1212
S5610
SCHEMBL40822
2-(1h-indol-3-yl)-acetamide
(1h-indol-3-yl)acetamide
1h-indol-3-yl-acetamide
SCHEMBL8082815
mfcd00005641
2-(1h-indol-3-yl)acetamide #
1-indole-3-acetamide
HB0341
AC-23418
HMS3604E11
DTXSID60236686
CS-W017500
IAM ,
indole-3-acetamide (8ci)
3-indole acetamide
879-06-1
HY-W016784
SY014237
Q27097844
BCP27037
SB15031
CCG-266389
1h-indol-3-ylacetamide
3-indolylacetamide;nsc 1969
EN300-74842
indole--d5-3-acetamide
1h-indole-3-ethanimidic acid
Z33546521
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (3)

RoleDescription
fungal metaboliteAny eukaryotic metabolite produced during a metabolic reaction in fungi, the kingdom that includes microorganisms such as the yeasts and moulds.
bacterial metaboliteAny prokaryotic metabolite produced during a metabolic reaction in bacteria.
plant metaboliteAny eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Drug Classes (3)

ClassDescription
indolesAny compound containing an indole skeleton.
N-acylammoniaA carboxamide obtained by the formal condensation of the carboxy group of any carboxylic acid with ammonia.
monocarboxylic acid amideA carboxamide derived from a monocarboxylic acid.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Pathways (6)

PathwayProteinsCompounds
indole-3-acetate biosynthesis III (bacteria)07
indole-3-acetate biosynthesis II820
indole-3-acetate biosynthesis IV (bacteria)07
indole-3-acetate biosynthesis II621
indole-3-acetate biosynthesis III (bacteria)411
IAA biosynthesis I025
Tryptophan metabolism2342
IAA biosynthesis VI (via indole-3-acetamide)07

Bioassays (2)

Assay IDTitleYearJournalArticle
AID540299A screen for compounds that inhibit the MenB enzyme of Mycobacterium tuberculosis2010Bioorganic & medicinal chemistry letters, Nov-01, Volume: 20, Issue:21
Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.
AID588519A screen for compounds that inhibit viral RNA polymerase binding and polymerization activities2011Antiviral research, Sep, Volume: 91, Issue:3
High-throughput screening identification of poliovirus RNA-dependent RNA polymerase inhibitors.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (56)

TimeframeStudies, This Drug (%)All Drugs %
pre-19902 (3.57)18.7374
1990's9 (16.07)18.2507
2000's21 (37.50)29.6817
2010's17 (30.36)24.3611
2020's7 (12.50)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 21.87

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index21.87 (24.57)
Research Supply Index4.06 (2.92)
Research Growth Index5.19 (4.65)
Search Engine Demand Index18.60 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (21.87)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews7 (12.28%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other50 (87.72%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]