The following articles (labelled with PubMed ID or TBD) are for your review
| PMID | Data | Article Title | Organization |
|---|
| 25922182 |
80 |
Synthesis and evaluation of quinazoline amino acid derivatives as mono amine oxidase (MAO) inhibitors. |
Alexandria University |
| 25466194 |
34 |
a-Ketoamino acid ester derivatives as promising MAO inhibitors. |
King Saud University |
| 25732770 |
12 |
Synthesis, biological investigation and molecular docking study of N-malonyl-1,2-dihydroisoquinoline derivatives as brain specific and shelf-stable MAO inhibitors. |
Assiut University |
| 25707011 |
52 |
Exploring new selective 3-benzylquinoxaline-based MAO-A inhibitors: design, synthesis, biological evaluation and docking studies. |
Alexandria University |
| 18281126 |
56 |
Synthesis, molecular modeling studies and selective inhibitory activity against MAO of N1-propanoyl-3,5-diphenyl-4,5-dihydro-(1H)-pyrazole derivatives. |
Sapienza University of Rome |
| 17266193 |
2 |
Monoamine oxidase isoform-dependent tautomeric influence in the recognition of 3,5-diaryl pyrazole inhibitors. |
Sapienza University of Rome |
| 23153282 |
70 |
Synthesis of new 7-oxycoumarin derivatives as potent and selective monoamine oxidase A inhibitors. |
National Research Center |
| 11881986 |
24 |
3-(1H-Pyrrol-1-yl)-2-oxazolidinones as reversible, highly potent, and selective inhibitors of monoamine oxidase type A. |
Sapienza University of Rome |
| 8246228 |
11 |
Transformation of heterocyclic reversible monoamine oxidase-B inactivators into irreversible inactivators by N-methylation. |
Northwestern University |
| 1548678 |
5 |
5-(Aminomethyl)-3-aryldihydrofuran-2(3H)-ones, a new class of monoamine oxidase-B inactivators. |
Northwestern University |
| 3397993 |
37 |
Stereoisomers of allenic amines as inactivators of monoamine oxidase type B. Stereochemical probes of the active site. |
Syntex Research |
| 22017497 |
34 |
Novel reversible monoamine oxidase A inhibitors: highly potent and selective 3-(1H-pyrrol-3-yl)-2-oxazolidinones. |
Sapienza University of Rome |
| 1593278 |
1 |
Metabolism of the Catharanthus Alkaloids: from Streptomyces griseus to Monoamine Oxidase B |
TBA |
| | 2 |
Selective inactivation of monoamine oxidase B by aminoethyl 3-chlorobenzyl ether |
TBA |
| 18951803 |
90 |
Synthesis, structure-activity relationships and molecular modeling studies of new indole inhibitors of monoamine oxidases A and B. |
Sapienza University of Rome |
| 16792415 |
3 |
Quercetin as the active principle of Hypericum hircinum exerts a selective inhibitory activity against MAO-A: extraction, biological analysis, and computational study. |
Sapienza University of Rome |
| 12620068 |
44 |
Simple, potent, and selective pyrrole inhibitors of monoamine oxidase types A and B. |
Sapienza University of Rome |
| 12443791 |
14 |
Inhibition of amine oxidases activity by 1-acetyl-3,5-diphenyl-4,5-dihydro-(1H)-pyrazole derivatives. |
Sapienza University of Rome |
| 27575476 |
30 |
Potent selective monoamine oxidase B inhibition by maackiain, a pterocarpan from the roots of Sophora flavescens. |
Sunchon National University |
| 9089337 |
3 |
4-substituted cubylcarbinylamines: a new class of mechanism-based monoamine oxidase B inactivators. |
Northwestern University |
| 8510099 |
6 |
Transformation of monoamine oxidase-B primary amine substrates into time-dependent inhibitors. Tertiary amine homologues of primary amine substrates. |
Northwestern University |
| 8474100 |
8 |
Inactivation of monoamine oxidase B by analogues of the anticonvulsant agent milacemide (2-(n-pentylamino)acetamide). |
Northwestern University |
| 17253676 |
36 |
Selective inhibitory activity against MAO and molecular modeling studies of 2-thiazolylhydrazone derivatives. |
Universit?????? Degli Studi Di Roma "La Sapienza |
| 16759860 |
14 |
Synthesis, molecular modeling studies, and selective inhibitory activity against monoamine oxidase of N,N'-bis[2-oxo-2H-benzopyran]-3-carboxamides. |
Universit£ |
| 9207939 |
9 |
Probing the active sites of monoamine oxidase A and B with 1,4-disubstituted tetrahydropyridine substrates and inactivators. |
Virginia Polytechnic Institute and State University |
| 2783613 |
4 |
Studies on semirigid tricyclic analogues of the nigrostriatal toxin 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine. |
University of California |
| 2362262 |
1 |
Vinblastine and vincristine are inhibitors of monoamine oxidase B. |
University of Iowa |
| 1433219 |
9 |
Synthesis of novel MPTP analogs as potential monoamine oxidase B (MAO-B) inhibitors. |
Virginia Polytechnic Institute and State University |
| 17416521 |
67 |
Discovery and structure-activity relationship studies of indole derivatives as liver X receptor (LXR) agonists. |
Tanabe Research Laboratories Usa |
| 17587573 |
33 |
2-Aryl-N-acyl indole derivatives as liver X receptor (LXR) agonists. |
Tanabe Research Laboratories Usa |
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