| Rho kinase (ROCK) inhibitors and their therapeutic potential Y Feng, PV LoGrasso, O Defert, R Li Journal of medicinal chemistry 59 (6), 2269-2300, 2016 | 375 | 2016 |
| Acetyl-terminated and template-assembled collagen-based polypeptides composed of Gly-Pro-Hyp sequences. 2. Synthesis and conformational analysis by circular dichroism … Y Feng, G Melacini, JP Taulane, M Goodman Journal of the American Chemical Society 118 (43), 10351-10358, 1996 | 255 | 1996 |
| A designed peptidomimetic agonistic ligand of TrkA nerve growth factor receptors S Maliartchouk, Y Feng, L Ivanisevic, T Debeir, AC Cuello, K Burgess, ... Molecular pharmacology 57 (2), 385-391, 2000 | 171 | 2000 |
| Pharmacologic inhibition of ROCK2 suppresses amyloid-β production in an Alzheimer's disease mouse model JH Herskowitz, Y Feng, AL Mattheyses, CM Hales, LA Higginbotham, ... Journal of Neuroscience 33 (49), 19086-19098, 2013 | 151 | 2013 |
| A Template-Induced Incipient Collagen-Like Triple-Helical Structure M Goodman, Y Feng, G Melacini, JP Taulane Journal of the American Chemical Society 118 (21), 5156-5157, 1996 | 128 | 1996 |
| Benzimidazole-and benzoxazole-based inhibitors of Rho kinase EH Sessions, Y Yin, TD Bannister, A Weiser, E Griffin, J Pocas, ... Bioorganic & medicinal chemistry letters 18 (24), 6390-6393, 2008 | 105 | 2008 |
| Discovery of substituted 4-(pyrazol-4-yl)-phenylbenzodioxane-2-carboxamides as potent and highly selective Rho kinase (ROCK-II) inhibitors Y Feng, Y Yin, A Weiser, E Griffin, MD Cameron, L Lin, C Ruiz, ... Journal of medicinal chemistry 51 (21), 6642-6645, 2008 | 98 | 2008 |
| Development of highly selective casein kinase 1δ/1ε (CK1δ/ε) inhibitors with potent antiproliferative properties M Bibian, RJ Rahaim, JY Choi, Y Noguchi, S Schürer, W Chen, ... Bioorganic & medicinal chemistry letters 23 (15), 4374-4380, 2013 | 96 | 2013 |
| SNAr Cyclizations To Form Cyclic Peptidomimetics of β-Turns Y Feng, Z Wang, S Jin, K Burgess Journal of the American Chemical Society 120 (41), 10768-10769, 1998 | 91 | 1998 |
| Collagen‐based structures containing the peptoid residue N‐isobutylglycine (Nleu): Synthesis and biophysical studies of Gly‐Pro‐Nleu sequences by circular dichroism … Y Feng, G Melacini, JP Taulane, M Goodman Biopolymers 39 (6), 859-872, 1996 | 88 | 1996 |
| Rho kinase inhibition as a therapeutic for progressive supranuclear palsy and corticobasal degeneration EG Gentry, BW Henderson, AE Arrant, M Gearing, Y Feng, NC Riddle, ... Journal of Neuroscience 36 (4), 1316-1323, 2016 | 85 | 2016 |
| Rho kinase (ROCK) inhibitors and their application to inflammatory disorders PV LoGrasso, Y Feng Current topics in medicinal chemistry 9 (8), 704-723, 2009 | 85 | 2009 |
| Collagen-like triple helices incorporating peptoid residues M Goodman, G Melacini, Y Feng Journal of the American Chemical Society 118 (44), 10928-10929, 1996 | 79 | 1996 |
| Collagen-Based Structures Containing the Peptoid Residue N-Isobutylglycine (Nleu): Synthesis and Biophysical Studies of Gly-Nleu-Pro Sequences by Circular … Y Feng, G Melacini, M Goodman Biochemistry 36 (29), 8716-8724, 1997 | 76 | 1997 |
| Solid-Phase SN2 Macrocyclization Reactions To Form β-Turn Mimics Y Feng, M Pattarawarapan, Z Wang, K Burgess Organic Letters 1 (1), 121-124, 1999 | 74 | 1999 |
| Tetrahydroisoquinoline derivatives as highly selective and potent Rho kinase inhibitors X Fang, Y Yin, YT Chen, L Yao, B Wang, MD Cameron, L Lin, S Khan, ... Journal of medicinal chemistry 53 (15), 5727-5737, 2010 | 69 | 2010 |
| Acetyl-Terminated and Template-Assembled Collagen-Based Polypeptides Composed of Gly-Pro-Hyp Sequences. 3. Conformational Analysis by 1H-NMR and … G Melacini, Y Feng, M Goodman Journal of the American Chemical Society 118 (43), 10359-10364, 1996 | 68 | 1996 |
| Collagen-Based Structures Containing the Peptoid Residue N-Isobutylglycine (Nleu). 6. Conformational Analysis of Gly-Pro-Nleu Sequences by 1H NMR, CD, and … G Melacini, Y Feng, M Goodman Journal of the American Chemical Society 118 (44), 10725-10732, 1996 | 59 | 1996 |
| Bis-aryl urea derivatives as potent and selective LIM kinase (Limk) inhibitors Y Yin, K Zheng, N Eid, S Howard, JH Jeong, F Yi, J Guo, CM Park, ... Journal of medicinal chemistry 58 (4), 1846-1861, 2015 | 57 | 2015 |
| Design and synthesis of highly potent and isoform selective JNK3 inhibitors: SAR studies on aminopyrazole derivatives K Zheng, S Iqbal, P Hernandez, HJ Park, PV LoGrasso, Y Feng Journal of medicinal chemistry 57 (23), 10013-10030, 2014 | 57 | 2014 |
