The following articles (labelled with PubMed ID or TBD) are for your review
PMID | Data | Article Title | Organization |
16279783 |
12 |
Structural, mutagenic, and kinetic analysis of the binding of substrates and inhibitors of human phenylethanolamine N-methyltransferase. |
University of Michigan |
2738892 |
2 |
Tetrahydrothiadiazoloisoquinolines: synthesis and inhibition of phenylethanolamine-N-methyltransferase. |
Smith Kline & French Laboratories |
7252985 |
16 |
Inhibitors of phenylethanolamine N-methyltransferase and epinephrine biosynthesis. 3. Bis[tetrahydroisoquinoline]s. |
TBA |
11412985 |
62 |
Phenylethanolamine N-methyltransferase kinetics: bovine versus recombinant human enzyme. |
University of Kansas |
19171483 |
3 |
Time-dependent inactivation of human phenylethanolamine N-methyltransferase by 7-isothiocyanatotetrahydroisoquinoline. |
University of Michigan |
18457385 |
41 |
Recent developments in fragment-based drug discovery. |
Astex Therapeutics |
18024134 |
38 |
Synthesis of 4,5,6,7-tetrahydrothieno[3,2-c]pyridines and comparison with their isosteric 1,2,3,4-tetrahydroisoquinolines as inhibitors of phenylethanolamine N-methyltransferase. |
The University of Kansas |
17845018 |
6 |
Enzyme adaptation to inhibitor binding: a cryptic binding site in phenylethanolamine N-methyltransferase. |
University of Queensland |
17126018 |
12 |
Exploring the active site of phenylethanolamine N-methyltransferase with 1,2,3,4-tetrahydrobenz[h]isoquinoline inhibitors. |
University of Kansas |
16686536 |
19 |
Application of the Goldilocks effect to the design of potent and selective inhibitors of phenylethanolamine N-methyltransferase: balancing pKa and steric effects in the optimization of 3-methyl-1,2,3,4-tetrahydroisoquinoline inhibitors by beta-fluorination. |
University of Kansas |
16169723 |
28 |
Inhibitors of phenylethanolamine N-methyltransferase devoid of alpha2-adrenoceptor affinity. |
University of Kansas |
15771426 |
34 |
Nanomolar inhibitors of CNS epinephrine biosynthesis: (R)-(+)-3-fluoromethyl-7-(N-substituted aminosulfonyl)-1,2,3,4-tetrahydroisoquinolines as potent and highly selective inhibitors of phenylethanolamine N-methyltransferase1. |
University of Kansas |
15686930 |
15 |
Exploring the active site of phenylethanolamine N-methyltransferase with 3-hydroxyethyl- and 3-hydroxypropyl-7-substituted-1,2,3,4-tetrahydroisoquinolines. |
University of Kansas |
15634007 |
17 |
3-hydroxymethyl-7-(N-substituted aminosulfonyl)-1,2,3,4-tetrahydroisoquinoline inhibitors of phenylethanolamine N-methyltransferase that display remarkable potency and selectivity. |
University of Kansas |
15317460 |
30 |
Inhibitors of phenylethanolamine N-methyltransferase that are predicted to penetrate the blood-brain barrier: design, synthesis, and evaluation of 3-fluoromethyl-7-(N-substituted aminosulfonyl)-1,2,3,4-tetrahydroisoquinolines that possess low affinity toward the alpha2-adrenoceptor. |
University of Kansas |
15261273 |
7 |
Phenylethanolamine N-methyltransferase inhibition: re-evaluation of kinetic data. |
University of Michigan |
31724854 |
30 |
Novel Propargyl-Linked Bisubstrate Analogues as Tight-Binding Inhibitors for Nicotinamide |
TBA |
7381849 |
18 |
Inhibitors of phenylethanolamine N-methyltransferase and epinephrine biosynthesis. 1. Chloro-substituted 1,2,3,4-tetrahydroisoquinolines. |
TBA |
18434170 |
25 |
Synthesis of 5-chloro-N-aryl-1H-indole-2-carboxamide derivatives as inhibitors of human liver glycogen phosphorylase a. |
Astellas Pharma |