Page last updated: 2024-12-05

indolepropanol phosphate

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

Description

Indolepropanol phosphate (IPP) is a naturally occurring compound that has been identified in a variety of plant species. It is a derivative of indole-3-propionic acid (IPA), which is a precursor to auxin, a plant hormone that plays a key role in plant growth and development. IPP has been shown to have a number of biological activities, including antimicrobial, antioxidant, and anti-inflammatory effects. It has also been suggested to have potential therapeutic applications in the treatment of cancer and other diseases. The synthesis of IPP has been studied using various enzymatic and chemical methods. The effects of IPP on plant growth and development have been investigated in various studies, showing its potential role in regulating auxin biosynthesis and signaling. The importance of IPP lies in its potential applications in agriculture, medicine, and biotechnology. Further research is needed to fully understand the biological activities and therapeutic potential of IPP.'

indolepropanol phosphate: binds specifically to the alpha subunit, but not to the beta subunit of tryptophan synthase [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

3-(indol-3-yl)propyl phosphate : An monoalkyl phosphate compound having an O-3-(indol-3-yl)propyl substituent. [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 CID3713
CHEMBL ID74074
CHEBI ID28162
SCHEMBL ID4317964
MeSH IDM0122471

Synonyms (20)

Synonym
CHEMBL74074 ,
indole-3-propanol phosphate
40716-80-1
1-(indol-3-yl)propanol 3-phosphate
indolepropanol phosphate
C04229
DB03171
CHEBI:28162 ,
3-(1h-indol-3-yl)propyl dihydrogen phosphate
3-(indol-3-yl)propyl phosphate
indole propanol phosphate
SCHEMBL4317964
unii-ko9j17s3fi
ko9j17s3fi ,
1h-indole-3-propanol, dihydrogen phosphate (ester)
1h-indole-3-propanol, 3-(dihydrogen phosphate)
DTXSID00193709
bdbm50487976
indole-3-propyl phosphate
Q27094108
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (2)

ClassDescription
indolesAny compound containing an indole skeleton.
monoalkyl phosphate
[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]

Protein Targets (2)

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (3)

Processvia Protein(s)Taxonomy
tryptophan biosynthetic processTryptophan synthase alpha chainEscherichia coli K-12
aromatic amino acid family biosynthetic processTryptophan synthase alpha chainEscherichia coli K-12
tryptophan biosynthetic processTryptophan synthase alpha chainEscherichia coli K-12
tryptophan metabolic processTryptophan synthase alpha chainEscherichia coli K-12
tryptophan biosynthetic processTryptophan synthase beta chainEscherichia coli K-12
aromatic amino acid family biosynthetic processTryptophan synthase beta chainEscherichia coli K-12
tryptophan biosynthetic processTryptophan synthase beta chainEscherichia coli K-12
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (6)

Processvia Protein(s)Taxonomy
tryptophan synthase activityTryptophan synthase alpha chainEscherichia coli K-12
tryptophan synthase activityTryptophan synthase alpha chainEscherichia coli K-12
lyase activityTryptophan synthase alpha chainEscherichia coli K-12
molecular adaptor activityTryptophan synthase alpha chainEscherichia coli K-12
tryptophan synthase activityTryptophan synthase beta chainEscherichia coli K-12
tryptophan synthase activityTryptophan synthase beta chainEscherichia coli K-12
lyase activityTryptophan synthase beta chainEscherichia coli K-12
pyridoxal phosphate bindingTryptophan synthase beta chainEscherichia coli K-12
identical protein bindingTryptophan synthase beta chainEscherichia coli K-12
protein homodimerization activityTryptophan synthase beta chainEscherichia coli K-12
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (2)

Processvia Protein(s)Taxonomy
cytoplasmTryptophan synthase alpha chainEscherichia coli K-12
cytosolTryptophan synthase alpha chainEscherichia coli K-12
cytosolTryptophan synthase alpha chainEscherichia coli K-12
cytoplasmTryptophan synthase beta chainEscherichia coli K-12
cytosolTryptophan synthase beta chainEscherichia coli K-12
cytoplasmTryptophan synthase beta chainEscherichia coli K-12
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (3)

Assay IDTitleYearJournalArticle
AID1100699Binding affinity to tryptophan synthase alpha2/beta2 complex in Escherichia coli K-12 by equlibrium dialysis method1999Bioorganic & medicinal chemistry letters, Aug-16, Volume: 9, Issue:16
Rational herbicide design by inhibition of tryptophan biosynthesis.
AID1100708Inhibition of Salmonella enterica subsp. enterica serovar Typhimurium tryptophan synthase alpha subunit1999Bioorganic & medicinal chemistry letters, Aug-16, Volume: 9, Issue:16
Rational herbicide design by inhibition of tryptophan biosynthesis.
AID213528Compound was tested for binding affinity against tryptophan synthase (K87T)2002Journal of medicinal chemistry, Jun-06, Volume: 45, Issue:12
Simple, intuitive calculations of free energy of binding for protein-ligand complexes. 1. Models without explicit constrained water.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (18)

TimeframeStudies, This Drug (%)All Drugs %
pre-19903 (16.67)18.7374
1990's5 (27.78)18.2507
2000's3 (16.67)29.6817
2010's6 (33.33)24.3611
2020's1 (5.56)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 11.70

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 weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index11.70 (24.57)
Research Supply Index2.94 (2.92)
Research Growth Index4.65 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (11.70)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (5.56%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other17 (94.44%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]