Page last updated: 2024-12-10

5'-(4-methylphenyl)-2-spiro[1H-indole-3,2'-3H-1,3,4-thiadiazole]one

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

Cross-References

ID SourceID
PubMed CID3136666
CHEMBL ID235890
CHEBI ID125151
SCHEMBL ID4351836

Synonyms (14)

Synonym
EU-0014533
TIMTEC1_004043
thiadiazole derivative, 13
bdbm23998
5''-(4-methylphenyl)-1,2-dihydro-3''h-spiro[indole-3,2''-[1,3,4]thiadiazole]-2-one
CHEBI:125151
HMS1545H17
CHEMBL235890
SCHEMBL4351836
5'-(4-methylphenyl)spiro[1h-indole-3,2'-3h-1,3,4-thiadiazole]-2-one
BRD-A41649729-001-01-0
AKOS024269833
Q27215495
5'-(4-methylphenyl)-2-spiro[1h-indole-3,2'-3h-1,3,4-thiadiazole]one
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (2)

ClassDescription
organooxygen compoundAn organochalcogen compound containing at least one carbon-oxygen bond.
organonitrogen compoundAny heteroorganic entity containing at least one carbon-nitrogen bond.
[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 (1)

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
A disintegrin and metalloproteinase with thrombospondin motifs 5Homo sapiens (human)IC50 (µMol)3.70000.50004.475010.0000AID1798388; AID301383
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (9)

Processvia Protein(s)Taxonomy
aortic valve morphogenesisA disintegrin and metalloproteinase with thrombospondin motifs 5Homo sapiens (human)
pulmonary valve morphogenesisA disintegrin and metalloproteinase with thrombospondin motifs 5Homo sapiens (human)
endocardial cushion morphogenesisA disintegrin and metalloproteinase with thrombospondin motifs 5Homo sapiens (human)
proteolysisA disintegrin and metalloproteinase with thrombospondin motifs 5Homo sapiens (human)
myoblast fusionA disintegrin and metalloproteinase with thrombospondin motifs 5Homo sapiens (human)
extracellular matrix disassemblyA disintegrin and metalloproteinase with thrombospondin motifs 5Homo sapiens (human)
defense response to bacteriumA disintegrin and metalloproteinase with thrombospondin motifs 5Homo sapiens (human)
negative regulation of cold-induced thermogenesisA disintegrin and metalloproteinase with thrombospondin motifs 5Homo sapiens (human)
extracellular matrix organizationA disintegrin and metalloproteinase with thrombospondin motifs 5Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (10)

Processvia Protein(s)Taxonomy
endopeptidase activityA disintegrin and metalloproteinase with thrombospondin motifs 5Homo sapiens (human)
metalloendopeptidase activityA disintegrin and metalloproteinase with thrombospondin motifs 5Homo sapiens (human)
integrin bindingA disintegrin and metalloproteinase with thrombospondin motifs 5Homo sapiens (human)
protein bindingA disintegrin and metalloproteinase with thrombospondin motifs 5Homo sapiens (human)
heparin bindingA disintegrin and metalloproteinase with thrombospondin motifs 5Homo sapiens (human)
peptidase activityA disintegrin and metalloproteinase with thrombospondin motifs 5Homo sapiens (human)
metallopeptidase activityA disintegrin and metalloproteinase with thrombospondin motifs 5Homo sapiens (human)
zinc ion bindingA disintegrin and metalloproteinase with thrombospondin motifs 5Homo sapiens (human)
identical protein bindingA disintegrin and metalloproteinase with thrombospondin motifs 5Homo sapiens (human)
extracellular matrix bindingA disintegrin and metalloproteinase with thrombospondin motifs 5Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (5)

Processvia Protein(s)Taxonomy
extracellular regionA disintegrin and metalloproteinase with thrombospondin motifs 5Homo sapiens (human)
extracellular spaceA disintegrin and metalloproteinase with thrombospondin motifs 5Homo sapiens (human)
endoplasmic reticulum lumenA disintegrin and metalloproteinase with thrombospondin motifs 5Homo sapiens (human)
collagen-containing extracellular matrixA disintegrin and metalloproteinase with thrombospondin motifs 5Homo sapiens (human)
extracellular matrixA disintegrin and metalloproteinase with thrombospondin motifs 5Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (6)

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.
AID1794808Fluorescence-based screening to identify small molecule inhibitors of Plasmodium falciparum apicoplast DNA polymerase (Pf-apPOL).2014Journal of biomolecular screening, Jul, Volume: 19, Issue:6
A High-Throughput Assay to Identify Inhibitors of the Apicoplast DNA Polymerase from Plasmodium falciparum.
AID1794808Fluorescence-based screening to identify small molecule inhibitors of Plasmodium falciparum apicoplast DNA polymerase (Pf-apPOL).
AID1798388ADAMTS-5 Inhibition Assay from Article 10.1016/j.bmcl.2007.07.048: \\5'-Phenyl-3'H-spiro[indoline-3,2'-[1,3,4]thiadiazol]-2-one inhibitors of ADAMTS-5 (aggrecanase-2).\\2007Bioorganic & medicinal chemistry letters, Oct-15, Volume: 17, Issue:20
5'-Phenyl-3'H-spiro[indoline-3,2'-[1,3,4]thiadiazol]-2-one inhibitors of ADAMTS-5 (aggrecanase-2).
AID301383Inhibition of ADAMTS5 by FRET assay2007Bioorganic & medicinal chemistry letters, Oct-15, Volume: 17, Issue:20
5'-Phenyl-3'H-spiro[indoline-3,2'-[1,3,4]thiadiazol]-2-one inhibitors of ADAMTS-5 (aggrecanase-2).
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (5)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (20.00)29.6817
2010's3 (60.00)24.3611
2020's1 (20.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 12.72

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 Index12.72 (24.57)
Research Supply Index1.79 (2.92)
Research Growth Index4.51 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.72)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other5 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]