The following articles (labelled with PubMed ID or TBD) are for your review
PMID | Data | Article Title | Organization |
28107736 |
53 |
Crystal structures, binding interactions, and ADME evaluation of brain penetrant N-substituted indazole-5-carboxamides as subnanomolar, selective monoamine oxidase B and dual MAO-A/B inhibitors. |
Ntz Lab |
3968682 |
20 |
Enzyme-activated irreversible inhibitors of monoamine oxidase: phenylallylamine structure-activity relationships. |
TBA |
6864731 |
38 |
Synthesis and monoamine oxidase inhibitory activities of alpha-allenic amines in vivo and in vitro. Different activities of two enantiomeric allenes. |
TBA |
27692996 |
84 |
Neuroprotective effects of benzyloxy substituted small molecule monoamine oxidase B inhibitors in Parkinson's disease. |
China Pharmaceutical University |
27578245 |
46 |
2-Benzylidene-1-indanone derivatives as inhibitors of monoamine oxidase. |
North-West University |
26652247 |
60 |
3-(Piperidin-4-ylmethoxy)pyridine Containing Compounds Are Potent Inhibitors of Lysine Specific Demethylase 1. |
Baylor College of Medicine |
26107513 |
172 |
Structure-Based Design and Optimization of Multitarget-Directed 2H-Chromen-2-one Derivatives as Potent Inhibitors of Monoamine Oxidase B and Cholinesterases. |
Universit£ |
25627172 |
150 |
Novel arylalkenylpropargylamines as neuroprotective, potent, and selective monoamine oxidase B inhibitors for the treatment of Parkinson's disease. |
A* Star |
25418133 |
51 |
N-Methyl-N-((1-methyl-5-(3-(1-(2-methylbenzyl)piperidin-4-yl)propoxy)-1H-indol-2-yl)methyl)prop-2-yn-1-amine, a new cholinesterase and monoamine oxidase dual inhibitor. |
Laboratorio De Quimica Medica (Iqog, Csic) |
25600407 |
26 |
Reversible and irreversible small molecule inhibitors of monoamine oxidase B (MAO-B) investigated by biophysical techniques. |
Dart Neuroscience |
24955776 |
166 |
Indazole- and indole-5-carboxamides: selective and reversible monoamine oxidase B inhibitors with subnanomolar potency. |
University of Bonn |
25462230 |
80 |
In silico design of novel 2H-chromen-2-one derivatives as potent and selective MAO-B inhibitors. |
Universit£ |
24813882 |
41 |
Donepezil + propargylamine + 8-hydroxyquinoline hybrids as new multifunctional metal-chelators, ChE and MAO inhibitors for the potential treatment of Alzheimer's disease. |
Okayama University |
23437843 |
30 |
Discovery, biological evaluation, and structure-activity and -selectivity relationships of 6'-substituted (E)-2-(benzofuran-3(2H)-ylidene)-N-methylacetamides, a novel class of potent and selective monoamine oxidase inhibitors. |
Universit£ |
16884303 |
27 |
Structural insights into monoamine oxidase inhibitory potency and selectivity of 7-substituted coumarins from ligand- and target-based approaches. |
Universit£ |
11543689 |
34 |
Coumarins derivatives as dual inhibitors of acetylcholinesterase and monoamine oxidase. |
Universit£ |
17034132 |
122 |
Impact of species-dependent differences on screening, design, and development of MAO B inhibitors. |
University of Geneva |
11123983 |
112 |
Inhibition of monoamine oxidases by functionalized coumarin derivatives: biological activities, QSARs, and 3D-QSARs. |
Universit£ |
22385498 |
24 |
Synthesis and evaluation of a set of para-substituted 4-phenylpiperidines and 4-phenylpiperazines as monoamine oxidase (MAO) inhibitors. |
Neurosearch Sweden |
22282722 |
10 |
Molecular Insights into Human Monoamine Oxidase B Inhibition by the Glitazone Anti-Diabetes Drugs. |
TBA |
22503231 |
66 |
Multipotent MAO and cholinesterase inhibitors for the treatment of Alzheimer's disease: synthesis, pharmacological analysis and molecular modeling of heterocyclic substituted alkyl and cycloalkyl propargyl amine. |
Laboratorio De Radicales Libres Y Qu�Mica Computacional (Iqog, Csic) |
22475561 |
42 |
Synthesis and inhibitory effect of piperine derivates on monoamine oxidase. |
General Hospital of Pla |
21175212 |
3 |
Interactions of monoamine oxidases with the antiepileptic drug zonisamide: specificity of inhibition and structure of the human monoamine oxidase B complex. |
University of Pavia |
20123154 |
48 |
2-Arylthiomorpholine derivatives as potent and selective monoamine oxidase B inhibitors. |
University of Chile |
19243954 |
36 |
Naphthylisopropylamine and N-benzylamphetamine derivatives as monoamine oxidase inhibitors. |
University of Chile |
17611112 |
36 |
A new therapeutic approach in Alzheimer disease: some novel pyrazole derivatives as dual MAO-B inhibitors and antiinflammatory analgesics. |
Hacettepe University |
15689151 |
112 |
Alkylamino derivatives of 4-aminomethylpyridine as inhibitors of copper-containing amine oxidases. |
Universit£ |
9258353 |
45 |
Selective inhibitors of monoamine oxidase. 4. SAR of tricyclic N-methylcarboxamides and congeners binding at the tricyclics' hydrophilic binding site. |
Wellcome Research Laboratories |
8487255 |
84 |
5-[4-(benzyloxy)phenyl]-1,3,4-oxadiazol-2(3H)-one derivatives and related analogues: new reversible, highly potent, and selective monamine oxidase type B inhibitors. |
Universit£ |
1433183 |
32 |
Aliphatic propargylamines: potent, selective, irreversible monoamine oxidase B inhibitors. |
University of Saskatchewan |
3397993 |
37 |
Stereoisomers of allenic amines as inactivators of monoamine oxidase type B. Stereochemical probes of the active site. |
Syntex Research |
7200144 |
2 |
(+/-)-4-Aryl-4,5-dihydro-3H-1,3-benzodiazepines. 1. Synthesis and evaluation of (+/-)-4,5-dihydro-2,3-dimethyl-4-phenyl-3H-1,3-benzodiazepine and analogues as potential antidepressant agents. |
TBA |
| 37 |
Alkylbenzyl ethers of hydroquinones as monoamine oxidase B inhibitors |
TBA |
| 51 |
Synthesis of coumarins as subtype-selective inhibitors of monoamine oxidase |
TBA |
22023459 |
42 |
Synthesis, biological evaluation, and molecular modeling of donepezil and N-[(5-(benzyloxy)-1-methyl-1H-indol-2-yl)methyl]-N-methylprop-2-yn-1-amine hybrids as new multipotent cholinesterase/monoamine oxidase inhibitors for the treatment of Alzheimer's disease. |
Universitat Aut£Noma De Barcelona |
21377879 |
44 |
Development of selective and reversible pyrazoline based MAO-B inhibitors: virtual screening, synthesis and biological evaluation. |
Birla Institute of Technology |
20117937 |
56 |
Design of novel nicotinamides as potent and selective monoamine oxidase a inhibitors. |
Nanjing University |
19969454 |
7 |
Proposed structural basis of interaction of piperine and related compounds with monoamine oxidases. |
University of Cambridge |
19945874 |
24 |
Towards development of selective and reversible pyrazoline based MAO-inhibitors: Synthesis, biological evaluation and docking studies. |
Institute of Technology |
19682910 |
48 |
Synthesis and molecular modeling of some novel hexahydroindazole derivatives as potent monoamine oxidase inhibitors. |
Hacettepe University |
19810674 |
93 |
Discovery of a novel class of potent coumarin monoamine oxidase B inhibitors: development and biopharmacological profiling of 7-[(3-chlorobenzyl)oxy]-4-[(methylamino)methyl]-2H-chromen-2-one methanesulfonate (NW-1772) as a highly potent, selective, reversible, and orally active monoamine oxidase B |
Universita Degli Studi Di Bari |
19091581 |
128 |
New pyrazoline bearing 4(3H)-quinazolinone inhibitors of monoamine oxidase: synthesis, biological evaluation, and structural determinants of MAO-A and MAO-B selectivity. |
Hacettepe University |
19064321 |
37 |
Ultrasound promoted synthesis of 2-imidazolines in water: a greener approach toward monoamine oxidase inhibitors. |
Universidade Federal De Santa Maria |
19053775 |
4 |
Structural and mechanistic studies of mofegiline inhibition of recombinant human monoamine oxidase B. |
Emory University |
18980841 |
72 |
Pyrazoline-based mycobactin analogues as MAO-inhibitors. |
Institute of Technology |
17824599 |
39 |
Solid-phase synthesis and insights into structure-activity relationships of safinamide analogues as potent and selective inhibitors of type B monoamine oxidase. |
University of Bari |
17521909 |
15 |
Human and rat monoamine oxidase-A are differentially inhibited by (S)-4-alkylthioamphetamine derivatives: insights from molecular modeling studies. |
University of Santiago De Chile |
16942031 |
4 |
3-[5-(4,5-dihydro-1H-imidazol-2-yl)-furan-2-yl]phenylamine (Amifuraline), a promising reversible and selective peripheral MAO-A inhibitor. |
Università |
16759116 |
8 |
Synthesis, structural reassignment, and biological activity of type B MAO inhibitors based on the 5H-indeno[1,2-c]pyridazin-5-one core. |
FacultéS Universitaires N.D. De La Paix |
16356714 |
16 |
Synthesis of 3-benzyl-2-substituted quinoxalines as novel monoamine oxidase A inhibitors. |
University of Alexandria |
15189042 |
24 |
Novel pyridazino[4,3-b]indoles with dual inhibitory activity against Mycobacterium tuberculosis and monoamine oxidase. |
Russian Academy of Sciences |
12127518 |
23 |
The synthesis and biological evaluation of a novel series of antimicrobials of the oxazolidinone class. |
Abbott Laboratories |
11591508 |
18 |
Synthesis of N-propargylphenelzine and analogues as neuroprotective agents. |
Cv Technologies |
10794685 |
42 |
Molecular determinants of MAO selectivity in a series of indolylmethylamine derivatives: biological activities, 3D-QSAR/CoMFA analysis, and computational simulation of ligand recognition. |
Universitat AutòNoma De Barcelona |
9748356 |
28 |
Inhibition of monoamine oxidase-B by condensed pyridazines and pyrimidines: effects of lipophilicity and structure-activity relationships. |
Université |
9622553 |
42 |
Selective inhibitors of monoamine oxidase (MAO). 5. 1-Substituted phenoxathiin inhibitors containing no nitrogen that inhibit MAO A by binding it to a hydrophobic site. |
The Wellcome Research Laboratories |
8627609 |
51 |
Selective inhibitors of monoamine oxidase. 3. Structure-activity relationship of tricyclics bearing imidazoline, oxadiazole, or tetrazole groups. |
Wellcome Research Laboratories |
8027990 |
25 |
Selective inhibitors of monoamine oxidase. 2. Arylamide SAR. |
Burroughs Wellcome |
7562919 |
132 |
Inhibition of monoamine oxidase-B by 5H-indeno[1,2-c]pyridazines: biological activities, quantitative structure-activity relationships (QSARs) and 3D-QSARs. |
Université |
7490728 |
87 |
Selective and potent monoamine oxidase type B inhibitors: 2-substituted 5-aryltetrazole derivatives. |
Université |
3735309 |
50 |
Selective monoamine oxidase inhibitors. 3. Cyclic compounds related to 4-aminophenethylamine. Preparation and neuron-selective action of some 5-(2-aminoethyl)-2,3-dihydroindoles. |
TBA |
2704029 |
44 |
Synthesis of some novel potent and selective catechol O-methyltransferase inhibitors. |
Orion |
14709324 |
20 |
Pharmacological profile of YM348, a novel, potent and orally active 5-HT2C receptor agonist. |
Yamanouchi Pharmaceutical |
17416521 |
67 |
Discovery and structure-activity relationship studies of indole derivatives as liver X receptor (LXR) agonists. |
Tanabe Research Laboratories Usa |
17373783 |
62 |
Discovery, synthesis, and in vivo activity of a new class of pyrazoloquinazolines as selective inhibitors of aurora B kinase. |
Astrazeneca |