Page last updated: 2024-11-11

3-hydroxy-4-methoxybenzaldehyde thiosemicarbazone

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

Description

3-hydroxy-4-methoxybenzaldehyde thiosemicarbazone: inhibits cabbage butterfly larvae phenoloxidase; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID6870649
CHEMBL ID242103
MeSH IDM0517198

Synonyms (7)

Synonym
bdbm50241211
3-hydroxy-4-methoxybenzaldehyde thiosemicarbazone
(e)-1-(3-hydroxy-4-methoxybenzylidene)thiosemicarbazide
CHEMBL242103 ,
AKOS002234001
[(e)-(3-hydroxy-4-methoxyphenyl)methylideneamino]thiourea
(e)-2-(3-hydroxy-4-methoxybenzylidene)hydrazinecarbothioamide
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Protein Targets (3)

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Polyphenol oxidase 2Agaricus bisporusIC50 (µMol)4.88000.03403.987110.0000AID1571721
CruzipainTrypanosoma cruziIC50 (µMol)10.00000.00022.04508.0000AID51390
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (10)

Assay IDTitleYearJournalArticle
AID1735990Antiproliferative activity against human Bel-7402 cells assessed as cell growth inhibition at 20 uM incubated for 48 hrs by MTT assay relative to control2019Journal of medicinal chemistry, 03-28, Volume: 62, Issue:6
Discovery of Novel Bromophenol-Thiosemicarbazone Hybrids as Potent Selective Inhibitors of Poly(ADP-ribose) Polymerase-1 (PARP-1) for Use in Cancer.
AID1504555Inhibition of Bothrops pauloensis MP1 assessed as reduction in azocaseinolytic activity after 30 mins2017ACS medicinal chemistry letters, Nov-09, Volume: 8, Issue:11
Structure-Based Discovery of Thiosemicarbazone Metalloproteinase Inhibitors for Hemorrhage Treatment in Snakebites.
AID1735989Antiproliferative activity against human SK-OV-3 cells assessed as cell growth inhibition at 20 uM incubated for 48 hrs by MTT assay relative to control2019Journal of medicinal chemistry, 03-28, Volume: 62, Issue:6
Discovery of Novel Bromophenol-Thiosemicarbazone Hybrids as Potent Selective Inhibitors of Poly(ADP-ribose) Polymerase-1 (PARP-1) for Use in Cancer.
AID1735993Cytotoxicity against human HL7702 cells assessed as cell growth inhibition at 20 uM incubated for 48 hrs by MTT assay relative to control2019Journal of medicinal chemistry, 03-28, Volume: 62, Issue:6
Discovery of Novel Bromophenol-Thiosemicarbazone Hybrids as Potent Selective Inhibitors of Poly(ADP-ribose) Polymerase-1 (PARP-1) for Use in Cancer.
AID1735992Antiproliferative activity against human Caco-2 cells assessed as cell growth inhibition at 20 uM incubated for 48 hrs by MTT assay relative to control2019Journal of medicinal chemistry, 03-28, Volume: 62, Issue:6
Discovery of Novel Bromophenol-Thiosemicarbazone Hybrids as Potent Selective Inhibitors of Poly(ADP-ribose) Polymerase-1 (PARP-1) for Use in Cancer.
AID293934Inhibition of pieris rapae Phenoloxidase2007Bioorganic & medicinal chemistry, Mar-01, Volume: 15, Issue:5
3D-QSAR and molecular docking studies of benzaldehyde thiosemicarbazone, benzaldehyde, benzoic acid, and their derivatives as phenoloxidase inhibitors.
AID1735999Inhibition of human recombinant GST-tagged PARP-1 expressed in Escherichia coli at 100 nM incubated for 30 mins in presence and NAD by resazurin dye based fluorescence analysis relative to control2019Journal of medicinal chemistry, 03-28, Volume: 62, Issue:6
Discovery of Novel Bromophenol-Thiosemicarbazone Hybrids as Potent Selective Inhibitors of Poly(ADP-ribose) Polymerase-1 (PARP-1) for Use in Cancer.
AID1571721Inhibition of mushroom tyrosinase using L-dopa as substrate preincubated for 10 mins followed by substrate addition and measured for 1 min2019MedChemComm, Mar-01, Volume: 10, Issue:3
Thiosemicarbazones with tyrosinase inhibitory activity.
AID1735991Antiproliferative activity against human HepG2 cells assessed as cell growth inhibition at 20 uM incubated for 48 hrs by MTT assay relative to control2019Journal of medicinal chemistry, 03-28, Volume: 62, Issue:6
Discovery of Novel Bromophenol-Thiosemicarbazone Hybrids as Potent Selective Inhibitors of Poly(ADP-ribose) Polymerase-1 (PARP-1) for Use in Cancer.
AID51390Inhibitory activity against Trypanosoma cruzi cathepsin L-like protease (cruzain) was determined using purified recombinant protein2002Journal of medicinal chemistry, Jun-20, Volume: 45, Issue:13
Synthesis and structure-activity relationship study of potent trypanocidal thio semicarbazone inhibitors of the trypanosomal cysteine protease cruzain.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (6)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (50.00)29.6817
2010's3 (50.00)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 12.56

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 Index12.56 (24.57)
Research Supply Index1.95 (2.92)
Research Growth Index4.51 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.56)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (16.67%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other5 (83.33%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]