Page last updated: 2024-12-08

tv3326

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Cross-References

ID SourceID
PubMed CID208907
CHEMBL ID255231
CHEBI ID177484
SCHEMBL ID678895
MeSH IDM0383556

Synonyms (32)

Synonym
[(3r)-3-(prop-2-ynylamino)-2,3-dihydro-1h-inden-5-yl] n-ethyl-n-methylcarbamate
209394-27-4
CHEBI:177484
n-propargylaminoindan (r)18b.hcl
r-cpai
bdbm10750
(3r)-3-(prop-2-yn-1-ylamino)-2,3-dihydro-1h-inden-5-yl n-ethyl-n-methylcarbamate hydrochloride
aminoindan deriv. (r)18b
aminoindan deriv. (r)18b.hcl
ladostigil
tv-3326 free base
CHEMBL255231
(3r)-3-(prop-2-ynylamino)indan-5-yl ethyl(methyl)carbamate
tv3326
sw3h1usr4q ,
ladostigil [inn]
unii-sw3h1usr4q
n-propargyl-(3r)-aminoindan-5-yl) ethyl methyl carbamate
carbamic acid, ethyl(methyl)-, (3r)-2,3-dihydro-3-(2-propynylamino)-1h-inden-5-yl ester
(3r)-3-(prop-2-yn-1-ylamino)-2,3-dihydro-1h-inden-5-yl ethyl(methyl)carbamate
LHXOCOHMBFOVJS-OAHLLOKOSA-N
ethyl-methyl-carbamic acid (r)-3-prop-2-ynylamino-indan-5-yl ester
SCHEMBL678895
AKOS030531889
ladostigil free base
HY-10399
CS-0002592
Q374426
(r)-3-(prop-2-yn-1-ylamino)-2,3-dihydro-1h-inden-5-yl ethyl(methyl)carbamate
209349-27-4 (free base)
DTXSID101045854
carbamic acid, n-ethyl-n-methyl-, (3r)-2,3-dihydro-3-(2-propyn-1-ylamino)-1h-inden-5-yl ester
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
indanes
[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 (10)

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
AcetylcholinesteraseElectrophorus electricus (electric eel)IC50 (µMol)40.90000.00000.94539.9400AID1412305; AID759446
Amine oxidase [flavin-containing] BRattus norvegicus (Norway rat)IC50 (µMol)466.75600.00040.764912.5000AID1600694; AID1796508
Amine oxidase [flavin-containing] A Rattus norvegicus (Norway rat)IC50 (µMol)333.44500.00071.979812.5000AID1796508
Amine oxidase [flavin-containing] AHomo sapiens (human)IC50 (µMol)95.00000.00002.37899.7700AID1412302; AID1657007; AID314094
Amine oxidase [flavin-containing] AHomo sapiens (human)Ki222.33330.00192.379710.0000AID125561; AID1796579
AcetylcholinesteraseHomo sapiens (human)IC50 (µMol)210.05430.00000.933210.0000AID1525504; AID1657009; AID1796508; AID314091
Acetylcholinesterase Bos taurus (cattle)IC50 (µMol)30.30000.00000.61068.7000AID710238
Amine oxidase [flavin-containing] BHomo sapiens (human)IC50 (µMol)50.91670.00001.89149.5700AID1057002; AID1412303; AID1657008; AID314095; AID706470; AID759443
Amine oxidase [flavin-containing] BHomo sapiens (human)Ki217.66670.00061.777110.0000AID126542; AID1796579
Tyrosine-protein kinase SYKHomo sapiens (human)IC50 (µMol)0.48000.00010.826010.0000AID710237
CholinesteraseEquus caballus (horse)IC50 (µMol)1.98000.00002.22149.4000AID1412306; AID1657010
Carboxylic ester hydrolase Equus caballus (horse)IC50 (µMol)0.48000.00512.69848.5000AID710237
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (104)

Processvia Protein(s)Taxonomy
biogenic amine metabolic processAmine oxidase [flavin-containing] AHomo sapiens (human)
positive regulation of signal transductionAmine oxidase [flavin-containing] AHomo sapiens (human)
dopamine catabolic processAmine oxidase [flavin-containing] AHomo sapiens (human)
acetylcholine catabolic process in synaptic cleftAcetylcholinesteraseHomo sapiens (human)
regulation of receptor recyclingAcetylcholinesteraseHomo sapiens (human)
osteoblast developmentAcetylcholinesteraseHomo sapiens (human)
acetylcholine catabolic processAcetylcholinesteraseHomo sapiens (human)
cell adhesionAcetylcholinesteraseHomo sapiens (human)
nervous system developmentAcetylcholinesteraseHomo sapiens (human)
synapse assemblyAcetylcholinesteraseHomo sapiens (human)
receptor internalizationAcetylcholinesteraseHomo sapiens (human)
negative regulation of synaptic transmission, cholinergicAcetylcholinesteraseHomo sapiens (human)
amyloid precursor protein metabolic processAcetylcholinesteraseHomo sapiens (human)
positive regulation of protein secretionAcetylcholinesteraseHomo sapiens (human)
retina development in camera-type eyeAcetylcholinesteraseHomo sapiens (human)
acetylcholine receptor signaling pathwayAcetylcholinesteraseHomo sapiens (human)
positive regulation of cold-induced thermogenesisAcetylcholinesteraseHomo sapiens (human)
response to xenobiotic stimulusAmine oxidase [flavin-containing] BHomo sapiens (human)
response to toxic substanceAmine oxidase [flavin-containing] BHomo sapiens (human)
response to aluminum ionAmine oxidase [flavin-containing] BHomo sapiens (human)
response to selenium ionAmine oxidase [flavin-containing] BHomo sapiens (human)
negative regulation of serotonin secretionAmine oxidase [flavin-containing] BHomo sapiens (human)
phenylethylamine catabolic processAmine oxidase [flavin-containing] BHomo sapiens (human)
substantia nigra developmentAmine oxidase [flavin-containing] BHomo sapiens (human)
response to lipopolysaccharideAmine oxidase [flavin-containing] BHomo sapiens (human)
dopamine catabolic processAmine oxidase [flavin-containing] BHomo sapiens (human)
response to ethanolAmine oxidase [flavin-containing] BHomo sapiens (human)
positive regulation of dopamine metabolic processAmine oxidase [flavin-containing] BHomo sapiens (human)
hydrogen peroxide biosynthetic processAmine oxidase [flavin-containing] BHomo sapiens (human)
response to corticosteroneAmine oxidase [flavin-containing] BHomo sapiens (human)
protein import into nucleusTyrosine-protein kinase SYKHomo sapiens (human)
regulation of DNA-binding transcription factor activityTyrosine-protein kinase SYKHomo sapiens (human)
angiogenesisTyrosine-protein kinase SYKHomo sapiens (human)
cell activationTyrosine-protein kinase SYKHomo sapiens (human)
lymph vessel developmentTyrosine-protein kinase SYKHomo sapiens (human)
positive regulation of receptor internalizationTyrosine-protein kinase SYKHomo sapiens (human)
stimulatory C-type lectin receptor signaling pathwayTyrosine-protein kinase SYKHomo sapiens (human)
adaptive immune responseTyrosine-protein kinase SYKHomo sapiens (human)
macrophage activation involved in immune responseTyrosine-protein kinase SYKHomo sapiens (human)
neutrophil activation involved in immune responseTyrosine-protein kinase SYKHomo sapiens (human)
leukocyte activation involved in immune responseTyrosine-protein kinase SYKHomo sapiens (human)
serotonin secretion by plateletTyrosine-protein kinase SYKHomo sapiens (human)
negative regulation of inflammatory response to antigenic stimulusTyrosine-protein kinase SYKHomo sapiens (human)
protein phosphorylationTyrosine-protein kinase SYKHomo sapiens (human)
leukocyte cell-cell adhesionTyrosine-protein kinase SYKHomo sapiens (human)
integrin-mediated signaling pathwayTyrosine-protein kinase SYKHomo sapiens (human)
animal organ morphogenesisTyrosine-protein kinase SYKHomo sapiens (human)
regulation of platelet activationTyrosine-protein kinase SYKHomo sapiens (human)
regulation of tumor necrosis factor-mediated signaling pathwayTyrosine-protein kinase SYKHomo sapiens (human)
peptidyl-tyrosine phosphorylationTyrosine-protein kinase SYKHomo sapiens (human)
leukotriene biosynthetic processTyrosine-protein kinase SYKHomo sapiens (human)
calcium-mediated signalingTyrosine-protein kinase SYKHomo sapiens (human)
platelet activationTyrosine-protein kinase SYKHomo sapiens (human)
B cell differentiationTyrosine-protein kinase SYKHomo sapiens (human)
neutrophil chemotaxisTyrosine-protein kinase SYKHomo sapiens (human)
positive regulation of protein-containing complex assemblyTyrosine-protein kinase SYKHomo sapiens (human)
receptor internalizationTyrosine-protein kinase SYKHomo sapiens (human)
positive regulation of type I interferon productionTyrosine-protein kinase SYKHomo sapiens (human)
positive regulation of granulocyte macrophage colony-stimulating factor productionTyrosine-protein kinase SYKHomo sapiens (human)
positive regulation of interleukin-10 productionTyrosine-protein kinase SYKHomo sapiens (human)
positive regulation of interleukin-12 productionTyrosine-protein kinase SYKHomo sapiens (human)
positive regulation of interleukin-3 productionTyrosine-protein kinase SYKHomo sapiens (human)
positive regulation of interleukin-4 productionTyrosine-protein kinase SYKHomo sapiens (human)
positive regulation of interleukin-6 productionTyrosine-protein kinase SYKHomo sapiens (human)
positive regulation of interleukin-8 productionTyrosine-protein kinase SYKHomo sapiens (human)
positive regulation of tumor necrosis factor productionTyrosine-protein kinase SYKHomo sapiens (human)
positive regulation of mast cell cytokine productionTyrosine-protein kinase SYKHomo sapiens (human)
regulation of superoxide anion generationTyrosine-protein kinase SYKHomo sapiens (human)
positive regulation of superoxide anion generationTyrosine-protein kinase SYKHomo sapiens (human)
positive regulation of cell adhesion mediated by integrinTyrosine-protein kinase SYKHomo sapiens (human)
intracellular signal transductionTyrosine-protein kinase SYKHomo sapiens (human)
collagen-activated tyrosine kinase receptor signaling pathwayTyrosine-protein kinase SYKHomo sapiens (human)
Fc-epsilon receptor signaling pathwayTyrosine-protein kinase SYKHomo sapiens (human)
Fc-gamma receptor signaling pathway involved in phagocytosisTyrosine-protein kinase SYKHomo sapiens (human)
interleukin-3-mediated signaling pathwayTyrosine-protein kinase SYKHomo sapiens (human)
gamma-delta T cell differentiationTyrosine-protein kinase SYKHomo sapiens (human)
defense response to bacteriumTyrosine-protein kinase SYKHomo sapiens (human)
positive regulation of cysteine-type endopeptidase activity involved in apoptotic processTyrosine-protein kinase SYKHomo sapiens (human)
mast cell degranulationTyrosine-protein kinase SYKHomo sapiens (human)
positive regulation of mast cell degranulationTyrosine-protein kinase SYKHomo sapiens (human)
regulation of neutrophil degranulationTyrosine-protein kinase SYKHomo sapiens (human)
beta selectionTyrosine-protein kinase SYKHomo sapiens (human)
positive regulation of MAPK cascadeTyrosine-protein kinase SYKHomo sapiens (human)
innate immune responseTyrosine-protein kinase SYKHomo sapiens (human)
positive regulation of B cell differentiationTyrosine-protein kinase SYKHomo sapiens (human)
positive regulation of gamma-delta T cell differentiationTyrosine-protein kinase SYKHomo sapiens (human)
positive regulation of bone resorptionTyrosine-protein kinase SYKHomo sapiens (human)
positive regulation of alpha-beta T cell differentiationTyrosine-protein kinase SYKHomo sapiens (human)
positive regulation of alpha-beta T cell proliferationTyrosine-protein kinase SYKHomo sapiens (human)
blood vessel morphogenesisTyrosine-protein kinase SYKHomo sapiens (human)
positive regulation of peptidyl-tyrosine phosphorylationTyrosine-protein kinase SYKHomo sapiens (human)
regulation of phagocytosisTyrosine-protein kinase SYKHomo sapiens (human)
positive regulation of calcium-mediated signalingTyrosine-protein kinase SYKHomo sapiens (human)
B cell receptor signaling pathwayTyrosine-protein kinase SYKHomo sapiens (human)
positive regulation of killing of cells of another organismTyrosine-protein kinase SYKHomo sapiens (human)
regulation of ERK1 and ERK2 cascadeTyrosine-protein kinase SYKHomo sapiens (human)
cellular response to molecule of fungal originTyrosine-protein kinase SYKHomo sapiens (human)
cellular response to lipidTyrosine-protein kinase SYKHomo sapiens (human)
cellular response to low-density lipoprotein particle stimulusTyrosine-protein kinase SYKHomo sapiens (human)
positive regulation of monocyte chemotactic protein-1 productionTyrosine-protein kinase SYKHomo sapiens (human)
regulation of arachidonic acid secretionTyrosine-protein kinase SYKHomo sapiens (human)
regulation of platelet aggregationTyrosine-protein kinase SYKHomo sapiens (human)
positive regulation of cold-induced thermogenesisTyrosine-protein kinase SYKHomo sapiens (human)
positive regulation of TORC1 signalingTyrosine-protein kinase SYKHomo sapiens (human)
cellular response to lectinTyrosine-protein kinase SYKHomo sapiens (human)
cell surface receptor protein tyrosine kinase signaling pathwayTyrosine-protein kinase SYKHomo sapiens (human)
cell differentiationTyrosine-protein kinase SYKHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (32)

Processvia Protein(s)Taxonomy
protein bindingAmine oxidase [flavin-containing] AHomo sapiens (human)
primary amine oxidase activityAmine oxidase [flavin-containing] AHomo sapiens (human)
aliphatic amine oxidase activityAmine oxidase [flavin-containing] AHomo sapiens (human)
monoamine oxidase activityAmine oxidase [flavin-containing] AHomo sapiens (human)
flavin adenine dinucleotide bindingAmine oxidase [flavin-containing] AHomo sapiens (human)
amyloid-beta bindingAcetylcholinesteraseHomo sapiens (human)
acetylcholinesterase activityAcetylcholinesteraseHomo sapiens (human)
cholinesterase activityAcetylcholinesteraseHomo sapiens (human)
protein bindingAcetylcholinesteraseHomo sapiens (human)
collagen bindingAcetylcholinesteraseHomo sapiens (human)
hydrolase activityAcetylcholinesteraseHomo sapiens (human)
serine hydrolase activityAcetylcholinesteraseHomo sapiens (human)
acetylcholine bindingAcetylcholinesteraseHomo sapiens (human)
protein homodimerization activityAcetylcholinesteraseHomo sapiens (human)
laminin bindingAcetylcholinesteraseHomo sapiens (human)
amyloid-beta bindingAcetylcholinesterase Bos taurus (cattle)
protein bindingAcetylcholinesterase Bos taurus (cattle)
protein bindingAmine oxidase [flavin-containing] BHomo sapiens (human)
primary amine oxidase activityAmine oxidase [flavin-containing] BHomo sapiens (human)
electron transfer activityAmine oxidase [flavin-containing] BHomo sapiens (human)
identical protein bindingAmine oxidase [flavin-containing] BHomo sapiens (human)
aliphatic amine oxidase activityAmine oxidase [flavin-containing] BHomo sapiens (human)
monoamine oxidase activityAmine oxidase [flavin-containing] BHomo sapiens (human)
flavin adenine dinucleotide bindingAmine oxidase [flavin-containing] BHomo sapiens (human)
phosphotyrosine residue bindingTyrosine-protein kinase SYKHomo sapiens (human)
protein kinase activityTyrosine-protein kinase SYKHomo sapiens (human)
protein serine/threonine kinase activityTyrosine-protein kinase SYKHomo sapiens (human)
protein tyrosine kinase activityTyrosine-protein kinase SYKHomo sapiens (human)
non-membrane spanning protein tyrosine kinase activityTyrosine-protein kinase SYKHomo sapiens (human)
signaling receptor bindingTyrosine-protein kinase SYKHomo sapiens (human)
integrin bindingTyrosine-protein kinase SYKHomo sapiens (human)
protein bindingTyrosine-protein kinase SYKHomo sapiens (human)
ATP bindingTyrosine-protein kinase SYKHomo sapiens (human)
interleukin-15 receptor bindingTyrosine-protein kinase SYKHomo sapiens (human)
kinase activityTyrosine-protein kinase SYKHomo sapiens (human)
protein kinase bindingTyrosine-protein kinase SYKHomo sapiens (human)
phosphatase bindingTyrosine-protein kinase SYKHomo sapiens (human)
Toll-like receptor bindingTyrosine-protein kinase SYKHomo sapiens (human)
SH2 domain bindingTyrosine-protein kinase SYKHomo sapiens (human)
phospholipase bindingTyrosine-protein kinase SYKHomo sapiens (human)
scaffold protein bindingTyrosine-protein kinase SYKHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (24)

Processvia Protein(s)Taxonomy
mitochondrionAmine oxidase [flavin-containing] AHomo sapiens (human)
mitochondrial outer membraneAmine oxidase [flavin-containing] AHomo sapiens (human)
cytosolAmine oxidase [flavin-containing] AHomo sapiens (human)
mitochondrionAmine oxidase [flavin-containing] AHomo sapiens (human)
extracellular regionAcetylcholinesteraseHomo sapiens (human)
basement membraneAcetylcholinesteraseHomo sapiens (human)
extracellular spaceAcetylcholinesteraseHomo sapiens (human)
nucleusAcetylcholinesteraseHomo sapiens (human)
Golgi apparatusAcetylcholinesteraseHomo sapiens (human)
plasma membraneAcetylcholinesteraseHomo sapiens (human)
cell surfaceAcetylcholinesteraseHomo sapiens (human)
membraneAcetylcholinesteraseHomo sapiens (human)
neuromuscular junctionAcetylcholinesteraseHomo sapiens (human)
synaptic cleftAcetylcholinesteraseHomo sapiens (human)
synapseAcetylcholinesteraseHomo sapiens (human)
perinuclear region of cytoplasmAcetylcholinesteraseHomo sapiens (human)
side of membraneAcetylcholinesteraseHomo sapiens (human)
synapseAcetylcholinesterase Bos taurus (cattle)
side of membraneAcetylcholinesterase Bos taurus (cattle)
mitochondrionAmine oxidase [flavin-containing] BHomo sapiens (human)
mitochondrial envelopeAmine oxidase [flavin-containing] BHomo sapiens (human)
mitochondrial outer membraneAmine oxidase [flavin-containing] BHomo sapiens (human)
dendriteAmine oxidase [flavin-containing] BHomo sapiens (human)
neuronal cell bodyAmine oxidase [flavin-containing] BHomo sapiens (human)
mitochondrionAmine oxidase [flavin-containing] BHomo sapiens (human)
cytoplasmTyrosine-protein kinase SYKHomo sapiens (human)
nucleusTyrosine-protein kinase SYKHomo sapiens (human)
cytoplasmTyrosine-protein kinase SYKHomo sapiens (human)
cytosolTyrosine-protein kinase SYKHomo sapiens (human)
plasma membraneTyrosine-protein kinase SYKHomo sapiens (human)
early phagosomeTyrosine-protein kinase SYKHomo sapiens (human)
B cell receptor complexTyrosine-protein kinase SYKHomo sapiens (human)
protein-containing complexTyrosine-protein kinase SYKHomo sapiens (human)
T cell receptor complexTyrosine-protein kinase SYKHomo sapiens (human)
plasma membraneTyrosine-protein kinase SYKHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (54)

Assay IDTitleYearJournalArticle
AID1796579MAO A and MAO B Activity Measurements from Article 10.1021/jm0310885: \\Inactivation of purified human recombinant monoamine oxidases A and B by rasagiline and its analogues.\\2004Journal of medicinal chemistry, Mar-25, Volume: 47, Issue:7
Inactivation of purified human recombinant monoamine oxidases A and B by rasagiline and its analogues.
AID1796508Cholinesterase Inhibition Assay from Article 10.1021/jm020120c: \\Novel dual inhibitors of AChE and MAO derived from hydroxy aminoindan and phenethylamine as potential treatment for Alzheimer's disease.\\2002Journal of medicinal chemistry, Nov-21, Volume: 45, Issue:24
Novel dual inhibitors of AChE and MAO derived from hydroxy aminoindan and phenethylamine as potential treatment for Alzheimer's disease.
AID1657010Inhibition of equine serum butyrylcholinesterase using butyrylthiocholine as substrate preincubated for 60 mins followed by substrate addition by Ellman's method2020Journal of medicinal chemistry, 06-11, Volume: 63, Issue:11
Acetylene Group, Friend or Foe in Medicinal Chemistry.
AID1412306Inhibition of equine serum BuChE using S-butyrylthiocholine iodide as substrate pretreated for 10 mins followed by substrate addition and measured after 10 mins by Ellman's method
AID1412307Selectivity index, ratio of IC50 for electric eel AChE to IC50 for equine serum BuChE
AID1057004Inhibition of human recombinant MAO-A using p-tyramine as substrate assessed as formation of H2O2 at 100 uM preincubated for 15 mins under dark condition followed by substrate addition measured after 20 mins by fluorescence assay relative to control2013Bioorganic & medicinal chemistry, Dec-01, Volume: 21, Issue:23
Inhibition of cholinesterase and monoamine oxidase-B activity by Tacrine-Homoisoflavonoid hybrids.
AID125561Binding affinity towards monoamine oxidase A activity was measured using a kynuramine assay2004Journal of medicinal chemistry, Mar-25, Volume: 47, Issue:7
Inactivation of purified human recombinant monoamine oxidases A and B by rasagiline and its analogues.
AID1557446Invivo inhibition of MAO-B in po dosed rabbit brain relative to control2019MedChemComm, Dec-01, Volume: 10, Issue:12
Current and emerging therapeutic targets of alzheimer's disease for the design of multi-target directed ligands.
AID1656476In-vivo inhibition of MAO B in rat brain at 26 mg/kg, po relative to control2020Bioorganic & medicinal chemistry letters, 02-01, Volume: 30, Issue:3
Propargylamine-derived multi-target directed ligands for Alzheimer's disease therapy.
AID1557443Invivo inhibition of AChE in po dosed rabbit brain relative to control2019MedChemComm, Dec-01, Volume: 10, Issue:12
Current and emerging therapeutic targets of alzheimer's disease for the design of multi-target directed ligands.
AID126545Compound was evaluated for A 450 decay towards monoamine oxidase B enzyme; ND = not determined2004Journal of medicinal chemistry, Mar-25, Volume: 47, Issue:7
Inactivation of purified human recombinant monoamine oxidases A and B by rasagiline and its analogues.
AID126669Compound was evaluated for A 450 rise towards monoamine oxidase B enzyme; ND = not determined2004Journal of medicinal chemistry, Mar-25, Volume: 47, Issue:7
Inactivation of purified human recombinant monoamine oxidases A and B by rasagiline and its analogues.
AID126671Compound was evaluated for inactivation for monoamine oxidase B; ND = not determined2004Journal of medicinal chemistry, Mar-25, Volume: 47, Issue:7
Inactivation of purified human recombinant monoamine oxidases A and B by rasagiline and its analogues.
AID125567Compound was evaluated for A 450 decay towards monoamine oxidase A enzyme; ND = not determined2004Journal of medicinal chemistry, Mar-25, Volume: 47, Issue:7
Inactivation of purified human recombinant monoamine oxidases A and B by rasagiline and its analogues.
AID314095Inhibition of MAOB2008Journal of medicinal chemistry, Feb-14, Volume: 51, Issue:3
Multi-target-directed ligands to combat neurodegenerative diseases.
AID1657008Inhibition of human MAO-B2020Journal of medicinal chemistry, 06-11, Volume: 63, Issue:11
Acetylene Group, Friend or Foe in Medicinal Chemistry.
AID759445Inhibition of equine serum BuChE using butylthiocholine chloride as substrate preincubated for 15 mins followed by substrate addition measured every 1 min by Ellman's method2013Journal of medicinal chemistry, Jul-25, Volume: 56, Issue:14
Design, synthesis, and evaluation of multitarget-directed resveratrol derivatives for the treatment of Alzheimer's disease.
AID1412302Inhibition of human recombinant MAOA using kynuramine as substrate preincubated for 10 mins followed by substrate addition at 10 secs intervals measured after 20 mins by fluorescence assay
AID706469Inhibition of human recombinant MAOA assessed as H2O2 production by Amplex Red reagent-based assay2012Journal of medicinal chemistry, Oct-11, Volume: 55, Issue:19
Multitarget-directed benzylideneindanone derivatives: anti-β-amyloid (Aβ) aggregation, antioxidant, metal chelation, and monoamine oxidase B (MAO-B) inhibition properties against Alzheimer's disease.
AID126542Binding affinity towards monoamine oxidase B activity was measured using a benzylamine assay2004Journal of medicinal chemistry, Mar-25, Volume: 47, Issue:7
Inactivation of purified human recombinant monoamine oxidases A and B by rasagiline and its analogues.
AID314091Inhibition of human AchE2008Journal of medicinal chemistry, Feb-14, Volume: 51, Issue:3
Multi-target-directed ligands to combat neurodegenerative diseases.
AID710228Cytotoxicity against rat H9c2 cells assessed as cell viability in absence of H2O22012Journal of medicinal chemistry, Dec-13, Volume: 55, Issue:23
Carbamate derivatives of indolines as cholinesterase inhibitors and antioxidants for the treatment of Alzheimer's disease.
AID314094Inhibition of MAOA2008Journal of medicinal chemistry, Feb-14, Volume: 51, Issue:3
Multi-target-directed ligands to combat neurodegenerative diseases.
AID1587206Inhibition of apoptosis in human SK-N-SH cells assessed as increase in cleaved caspase-3 by Western blot analysis2019European journal of medicinal chemistry, May-01, Volume: 169Advancement of multi-target drug discoveries and promising applications in the field of Alzheimer's disease.
AID126056Inhibitory concentration towards monoamine oxidase A in rat brain was measured2004Journal of medicinal chemistry, Mar-25, Volume: 47, Issue:7
Inactivation of purified human recombinant monoamine oxidases A and B by rasagiline and its analogues.
AID1412305Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition and measured after 10 mins by Ellman's method
AID1657007Inhibition of human MAO-A2020Journal of medicinal chemistry, 06-11, Volume: 63, Issue:11
Acetylene Group, Friend or Foe in Medicinal Chemistry.
AID1525504Inhibition of AChE in human erythrocytes preincubated for 60 mins followed by substrate addition by Ellman's method2019Journal of medicinal chemistry, 10-24, Volume: 62, Issue:20
Rational Design of Multitarget-Directed Ligands: Strategies and Emerging Paradigms.
AID1057002Inhibition of human recombinant MAO-B using benzylamine as substrate preincubated for 15 mins under dark condition followed by substrate addition measured after 20 mins by fluorescence assay2013Bioorganic & medicinal chemistry, Dec-01, Volume: 21, Issue:23
Inhibition of cholinesterase and monoamine oxidase-B activity by Tacrine-Homoisoflavonoid hybrids.
AID1412303Inhibition of human recombinant MAOB using kynuramine as substrate preincubated for 10 mins followed by substrate addition at 10 secs intervals measured after 20 mins by fluorescence assay
AID1656475In-vivo inhibition of MAO A in rat brain at 26 mg/kg, po relative to control2020Bioorganic & medicinal chemistry letters, 02-01, Volume: 30, Issue:3
Propargylamine-derived multi-target directed ligands for Alzheimer's disease therapy.
AID710238Inhibition of bovine AChE after 120 mins by Ellman's method2012Journal of medicinal chemistry, Dec-13, Volume: 55, Issue:23
Carbamate derivatives of indolines as cholinesterase inhibitors and antioxidants for the treatment of Alzheimer's disease.
AID1545324In vivo inhibition of MAO-B in Sprague-Dawley rat at 26 mg/kg, po administered for 2 weeks by radioassay method relative to control2019Bioorganic & medicinal chemistry, 03-15, Volume: 27, Issue:6
Anti-cholinesterase hybrids as multi-target-directed ligands against Alzheimer's disease (1998-2018).
AID759444Inhibition of human recombinant MAOA using p-tyramine as substrate incubated for 15 mins prior to substrate addition measured after 20 mins by fluorescence plate reader analysis2013Journal of medicinal chemistry, Jul-25, Volume: 56, Issue:14
Design, synthesis, and evaluation of multitarget-directed resveratrol derivatives for the treatment of Alzheimer's disease.
AID1557445Invivo inhibition of MAO-B in po dosed rat brain relative to control2019MedChemComm, Dec-01, Volume: 10, Issue:12
Current and emerging therapeutic targets of alzheimer's disease for the design of multi-target directed ligands.
AID125571Compound was evaluated for inactivation for monoamine oxidase A; ND = not determined2004Journal of medicinal chemistry, Mar-25, Volume: 47, Issue:7
Inactivation of purified human recombinant monoamine oxidases A and B by rasagiline and its analogues.
AID710236Selectivity ratio of IC50 for equine BuChE to IC50 for bovine AChE2012Journal of medicinal chemistry, Dec-13, Volume: 55, Issue:23
Carbamate derivatives of indolines as cholinesterase inhibitors and antioxidants for the treatment of Alzheimer's disease.
AID1545325In vivo inhibition of MAO-A in Sprague-Dawley rat at 26 mg/kg, po administered for 2 weeks by radioassay method relative to control2019Bioorganic & medicinal chemistry, 03-15, Volume: 27, Issue:6
Anti-cholinesterase hybrids as multi-target-directed ligands against Alzheimer's disease (1998-2018).
AID710237Inhibition of equine BuChE after 120 mins by Ellman's method2012Journal of medicinal chemistry, Dec-13, Volume: 55, Issue:23
Carbamate derivatives of indolines as cholinesterase inhibitors and antioxidants for the treatment of Alzheimer's disease.
AID125569Compound was evaluated for A 450 rise towards monoamine oxidase A enzyme; ND = not determined2004Journal of medicinal chemistry, Mar-25, Volume: 47, Issue:7
Inactivation of purified human recombinant monoamine oxidases A and B by rasagiline and its analogues.
AID710226Prevention of apoptosis in rat H9c2 cells assessed as protection against oxidative stress-induced cytotoxicity at 100 nM pM by Alamar blue assay2012Journal of medicinal chemistry, Dec-13, Volume: 55, Issue:23
Carbamate derivatives of indolines as cholinesterase inhibitors and antioxidants for the treatment of Alzheimer's disease.
AID1412304Selectivity index, ratio of IC50 for human recombinant MAOA to IC50 for human recombinant MAOB
AID759443Inhibition of human recombinant MAOB using benzylamine as substrate incubated for 15 mins prior to substrate addition measured after 20 mins by fluorescence plate reader analysis2013Journal of medicinal chemistry, Jul-25, Volume: 56, Issue:14
Design, synthesis, and evaluation of multitarget-directed resveratrol derivatives for the treatment of Alzheimer's disease.
AID1657009Inhibition of human acetylcholinesterase using acetylthiocholine iodide as substrate preincubated for 60 mins followed by substrate addition by Ellman's method2020Journal of medicinal chemistry, 06-11, Volume: 63, Issue:11
Acetylene Group, Friend or Foe in Medicinal Chemistry.
AID706470Inhibition of human recombinant MAOB assessed as H2O2 production by Amplex Red reagent-based assay2012Journal of medicinal chemistry, Oct-11, Volume: 55, Issue:19
Multitarget-directed benzylideneindanone derivatives: anti-β-amyloid (Aβ) aggregation, antioxidant, metal chelation, and monoamine oxidase B (MAO-B) inhibition properties against Alzheimer's disease.
AID1557442Invivo inhibition of AChE in po dosed rat brain relative to control2019MedChemComm, Dec-01, Volume: 10, Issue:12
Current and emerging therapeutic targets of alzheimer's disease for the design of multi-target directed ligands.
AID1557441Invivo inhibition of AChE in po dosed mouse brain relative to control2019MedChemComm, Dec-01, Volume: 10, Issue:12
Current and emerging therapeutic targets of alzheimer's disease for the design of multi-target directed ligands.
AID759446Inhibition of electric eel AChE using acetylthiocholine chloride as substrate preincubated for 15 mins followed by substrate addition measured every 1 min by Ellman's method2013Journal of medicinal chemistry, Jul-25, Volume: 56, Issue:14
Design, synthesis, and evaluation of multitarget-directed resveratrol derivatives for the treatment of Alzheimer's disease.
AID1525505Inhibition of MAO-A in rat brain using [14C]-5-hydroxytryptamine creatinine disulfate as substrate preincubated for 60 mins followed by substrate addition and measured after 30 mins by liquid scintillation counting method2019Journal of medicinal chemistry, 10-24, Volume: 62, Issue:20
Rational Design of Multitarget-Directed Ligands: Strategies and Emerging Paradigms.
AID710227Prevention of apoptosis in rat H9c2 cells assessed as reduction in fall of mitochondrial membrane potential at 100 nM after 1 hr2012Journal of medicinal chemistry, Dec-13, Volume: 55, Issue:23
Carbamate derivatives of indolines as cholinesterase inhibitors and antioxidants for the treatment of Alzheimer's disease.
AID127007Inhibitory concentration towards monoamine oxidase B in rat brain was measured2004Journal of medicinal chemistry, Mar-25, Volume: 47, Issue:7
Inactivation of purified human recombinant monoamine oxidases A and B by rasagiline and its analogues.
AID1557444Invivo inhibition of MAO-B in po dosed mouse brain relative to control2019MedChemComm, Dec-01, Volume: 10, Issue:12
Current and emerging therapeutic targets of alzheimer's disease for the design of multi-target directed ligands.
AID1525506Inhibition of MAO-B in rat brain using [14C]-phenylethylamine as substrate preincubated for 60 mins followed by substrate addition and measured after 30 mins by liquid scintillation counting method2019Journal of medicinal chemistry, 10-24, Volume: 62, Issue:20
Rational Design of Multitarget-Directed Ligands: Strategies and Emerging Paradigms.
AID1600694Inhibition of rat brain MAO-B using [14C]-phenylethylamine as substrate preincubated for 60 mins followed by substrate addition and measured after 20 mins by liquid scintillation counting method2019Bioorganic & medicinal chemistry letters, 10-01, Volume: 29, Issue:19
Rasagiline derivatives combined with histamine H
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (15)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (20.00)29.6817
2010's10 (66.67)24.3611
2020's2 (13.33)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 12.25

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 Index12.25 (24.57)
Research Supply Index2.77 (2.92)
Research Growth Index5.03 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.25)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews6 (40.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other9 (60.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]