Page last updated: 2024-12-06

5-benzylhydantoin

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

Description

5-benzylhydantoin: structure given in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID73565
CHEMBL ID1914996
SCHEMBL ID1011632
MeSH IDM0098744

Synonyms (39)

Synonym
nsc 50842
nsc 30459
einecs 222-563-3
nsc-50842
nsc50842
3530-82-3
nsc-30459
nsc30459
5-benzylhydantoin
5-benzylimidazolidine-2,4-dione
2,4-imidazolidinedione, 5-(phenylmethyl)-
OPREA1_159971
MAYBRIDGE4_003425
SR-01000642834-1
NCGC00175858-01
HMS1530L15
BRD-A44258161-001-01-2
5-benzyl hydantoin
AKOS001073298
A822724
CCG-53684
CHEMBL1914996 ,
5-benzyl-2,4-imidazolidione
AKOS017268959
FT-0620039
SCHEMBL1011632
DBOMTIHROGSFTI-UHFFFAOYSA-N
d-5-benzylhydantoin
5-benzyl-hydantoine
5-benzylimidazolidin-2,4-dione
5-benzyl-hydantoin
mfcd00016634
W-106676
5-benzyl hydantoin, aldrichcpr
DTXSID40874065
bdbm50240918
CS-0307654
EN300-04257
Z56862344
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Protein Targets (1)

Activation Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Carbonic anhydrase 2Homo sapiens (human)Kd2,000.00000.00000.41575.5500AID1451276
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (12)

Processvia Protein(s)Taxonomy
morphogenesis of an epitheliumCarbonic anhydrase 2Homo sapiens (human)
positive regulation of synaptic transmission, GABAergicCarbonic anhydrase 2Homo sapiens (human)
positive regulation of cellular pH reductionCarbonic anhydrase 2Homo sapiens (human)
angiotensin-activated signaling pathwayCarbonic anhydrase 2Homo sapiens (human)
regulation of monoatomic anion transportCarbonic anhydrase 2Homo sapiens (human)
secretionCarbonic anhydrase 2Homo sapiens (human)
regulation of intracellular pHCarbonic anhydrase 2Homo sapiens (human)
neuron cellular homeostasisCarbonic anhydrase 2Homo sapiens (human)
positive regulation of dipeptide transmembrane transportCarbonic anhydrase 2Homo sapiens (human)
regulation of chloride transportCarbonic anhydrase 2Homo sapiens (human)
carbon dioxide transportCarbonic anhydrase 2Homo sapiens (human)
one-carbon metabolic processCarbonic anhydrase 2Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (5)

Processvia Protein(s)Taxonomy
arylesterase activityCarbonic anhydrase 2Homo sapiens (human)
carbonate dehydratase activityCarbonic anhydrase 2Homo sapiens (human)
protein bindingCarbonic anhydrase 2Homo sapiens (human)
zinc ion bindingCarbonic anhydrase 2Homo sapiens (human)
cyanamide hydratase activityCarbonic anhydrase 2Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (6)

Processvia Protein(s)Taxonomy
cytoplasmCarbonic anhydrase 2Homo sapiens (human)
cytosolCarbonic anhydrase 2Homo sapiens (human)
plasma membraneCarbonic anhydrase 2Homo sapiens (human)
myelin sheathCarbonic anhydrase 2Homo sapiens (human)
apical part of cellCarbonic anhydrase 2Homo sapiens (human)
extracellular exosomeCarbonic anhydrase 2Homo sapiens (human)
cytoplasmCarbonic anhydrase 2Homo sapiens (human)
plasma membraneCarbonic anhydrase 2Homo sapiens (human)
apical part of cellCarbonic anhydrase 2Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (11)

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).
AID628028Inhibition of cystine/glutamate transporter in human SNB19 cells assessed as [3H]glutamate uptake at 500 uM2011Bioorganic & medicinal chemistry letters, Jul-15, Volume: 21, Issue:14
Use of the hydantoin isostere to produce inhibitors showing selectivity toward the vesicular glutamate transporter versus the obligate exchange transporter system x(c)(-).
AID1451281Binding affinity to human carbonic anhydrase 2 at +10 charge state for protein to compound complex after 10 mins by nanoESI-MS method2017Journal of medicinal chemistry, 09-14, Volume: 60, Issue:17
Identification of a New Zinc Binding Chemotype by Fragment Screening.
AID1451278Binding affinity to human carbonic anhydrase 2 at +9, +10 and +11 charge states for protein to compound complex at 7.5 uM after 10 mins by nanoESI-MS method2017Journal of medicinal chemistry, 09-14, Volume: 60, Issue:17
Identification of a New Zinc Binding Chemotype by Fragment Screening.
AID1451280Binding affinity to human carbonic anhydrase 2 at +9, +10 and +11 charge states for protein to compound complex after 10 mins by nanoESI-MS method2017Journal of medicinal chemistry, 09-14, Volume: 60, Issue:17
Identification of a New Zinc Binding Chemotype by Fragment Screening.
AID1451276Binding affinity to human carbonic anhydrase 2 by surface plasmon resonance spectrometry2017Journal of medicinal chemistry, 09-14, Volume: 60, Issue:17
Identification of a New Zinc Binding Chemotype by Fragment Screening.
AID1451279Binding affinity to human carbonic anhydrase 2 at +10 charge state for protein to compound complex at 7.5 uM after 10 mins by nanoESI-MS method2017Journal of medicinal chemistry, 09-14, Volume: 60, Issue:17
Identification of a New Zinc Binding Chemotype by Fragment Screening.
AID628027Inhibition of VGLUT in rat synaptic vesicles assessed as glutamate uptake at 5 mM relative to control2011Bioorganic & medicinal chemistry letters, Jul-15, Volume: 21, Issue:14
Use of the hydantoin isostere to produce inhibitors showing selectivity toward the vesicular glutamate transporter versus the obligate exchange transporter system x(c)(-).
[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-19901 (5.56)18.7374
1990's0 (0.00)18.2507
2000's7 (38.89)29.6817
2010's9 (50.00)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: 12.28

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 Index12.28 (24.57)
Research Supply Index2.94 (2.92)
Research Growth Index5.23 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.28)

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%
Other18 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]