Year |
Citation |
Score |
2003 |
Owens TD, Souers AJ, Ellman JA. The preparation and utility of bis(sulfinyl)imidoamidine ligands for the copper-catalyzed Diels-Alder reaction. The Journal of Organic Chemistry. 68: 3-10. PMID 12515453 DOI: 10.1021/Jo020524C |
0.647 |
|
2002 |
Ellman JA, Owens TD, Tang TP. N-tert-butanesulfinyl imines: versatile intermediates for the asymmetric synthesis of amines. Accounts of Chemical Research. 35: 984-95. PMID 12437323 DOI: 10.1021/Ar020066U |
0.636 |
|
2001 |
Owens TD, Semple JE. Atom-economical synthesis of the N(10)-C(17) fragment of cyclotheonamides via a novel Passerini reaction-deprotection-acyl migration strategy. Organic Letters. 3: 3301-4. PMID 11594819 DOI: 10.1021/ol0165239 |
0.404 |
|
2001 |
Souers AJ, Owens TD, Oliver AG, Hollander FJ, Ellman JA. Synthesis and crystal structure of a unique and homochiral N,S-bonded N,N'-bis(tert-butanesulfinyl)amidinate rhodium(I) complex. Inorganic Chemistry. 40: 5299-301. PMID 11559098 DOI: 10.1021/Ic0104205 |
0.64 |
|
2001 |
Owens TD, Hollander FJ, Oliver AG, Ellman JA. Synthesis, utility, and structure of novel bis(sulfinyl)imidoamidine ligands for asymmetric Lewis acid catalysis [21] Journal of the American Chemical Society. 123: 1539-1540. DOI: 10.1021/Ja005635C |
0.635 |
|
2001 |
Owens TD, Araldi GL, Nutt RF, Semple JE. Concise total synthesis of the prolyl endopeptidase inhibitor eurystatin A via a novel Passerini reaction-deprotection-acyl migration strategy Tetrahedron Letters. 42: 6271-6274. DOI: 10.1016/S0040-4039(01)01287-4 |
0.435 |
|
2000 |
Semple JE, Owens TD, Nguyen K, Levy OE. New synthetic technology for efficient construction of alpha-hydroxy-beta-amino amides via the Passerini reaction. Organic Letters. 2: 2769-72. PMID 10964361 DOI: 10.1021/Ol0061485 |
0.484 |
|
1999 |
Liu G, Cogan DA, Owens TD, Tang TP, Ellman JA. Synthesis of enantiomerically pure N-tert-butanesulfinyl imines (tert- butanesulfinimines) by the direct condensation of tert-butanesulfinamide with aldehydes and ketones Journal of Organic Chemistry. 64: 1278-1284. DOI: 10.1021/Jo982059I |
0.637 |
|
1998 |
Owens TD, Semple JE. Alkoxide-catalyzed ring-opening of a novel homosaccharin derivative: synthesis of potent, selective P3-lactam thrombin inhibitors containing P4-o-alkoxycarbonylbenzylsulfonamide residues. Bioorganic & Medicinal Chemistry Letters. 8: 3683-8. PMID 9934495 DOI: 10.1016/S0960-894X(98)00667-2 |
0.368 |
|
Low-probability matches (unlikely to be authored by this person) |
2000 |
Semple JE, Levy OE, Minami NK, Owens TD, Siev DV. Novel, potent and selective chimeric FXa inhibitors featuring hydrophobic P1-ketoamide moieties. Bioorganic & Medicinal Chemistry Letters. 10: 2305-9. PMID 11055344 DOI: 10.1016/S0960-894X(00)00458-3 |
0.28 |
|
2001 |
Semple JE, Owens TD, Nguyen K, Levy OE. ChemInform Abstract: New Synthetic Technology for Efficient Construction of α-Hydroxy-β-amino Amides via the Passerini Reaction. Cheminform. 32: no-no. DOI: 10.1002/chin.200102082 |
0.21 |
|
2015 |
Lou Y, Sweeney ZK, Kuglstatter A, Davis D, Goldstein DM, Han X, Hong J, Kocer B, Kondru RK, Litman R, McIntosh J, Sarma K, Suh J, Taygerly J, Owens TD. Finding the perfect spot for fluorine: improving potency up to 40-fold during a rational fluorine scan of a Bruton's Tyrosine Kinase (BTK) inhibitor scaffold. Bioorganic & Medicinal Chemistry Letters. 25: 367-71. PMID 25466710 DOI: 10.1016/j.bmcl.2014.11.030 |
0.183 |
|
1996 |
Semple JE, Rowley DC, Brunck TK, Ha-Uong T, Minami NK, Owens TD, Tamura SY, Goldman EA, Siev DV, Ardecky RJ, Carpenter SH, Ge Y, Richard BM, Nolan TG, HÃ¥kanson K, et al. Design, synthesis, and evolution of a novel, selective, and orally bioavailable class of thrombin inhibitors: P1-argininal derivatives incorporating P3-P4 lactam sulfonamide moieties. Journal of Medicinal Chemistry. 39: 4531-6. PMID 8917639 DOI: 10.1021/jm960572n |
0.165 |
|
1998 |
Semple JE, Rowley DC, Owens TD, Minami NK, Uong TH, Brunck TK. Potent and selective thrombin inhibitors featuring hydrophobic, basic P3-P4-aminoalkyllactam moieties. Bioorganic & Medicinal Chemistry Letters. 8: 3525-30. PMID 9934465 DOI: 10.1016/S0960-894X(98)00636-2 |
0.139 |
|
2015 |
Lou Y, Han X, Kuglstatter A, Kondru RK, Sweeney ZK, Soth M, McIntosh J, Litman R, Suh J, Kocer B, Davis D, Park J, Frauchiger S, Dewdney N, Zecic H, ... ... Owens TD, et al. Structure-based drug design of RN486, a potent and selective Bruton's tyrosine kinase (BTK) inhibitor, for the treatment of rheumatoid arthritis. Journal of Medicinal Chemistry. 58: 512-6. PMID 24712864 DOI: 10.1021/jm500305p |
0.124 |
|
2016 |
Lou Y, Lopez F, Jiang Y, Han X, Brotherton C, Billedeau R, Gabriel S, Gleason S, Goldstein DM, Hilgenkamp R, Kocer B, Orzechowski L, Tan J, Wovkulich P, Wen B, ... ... Owens TD, et al. Mitigation of reactive metabolite formation for a series of 3-amino-2-pyridone inhibitors of Bruton's tyrosine kinase (BTK). Bioorganic & Medicinal Chemistry Letters. PMID 28025004 DOI: 10.1016/j.bmcl.2016.11.092 |
0.12 |
|
2021 |
Owens TD, Smith PF, Redfern A, Xing Y, Shu J, Karr DE, Hartmann S, Francesco MR, Langrish CL, Nunn PA, Gourlay SG. Phase 1 Clinical Trial Evaluating Safety, Exposure and Pharmacodynamics of BTK Inhibitor Tolebrutinib (PRN2246, SAR442168). Clinical and Translational Science. PMID 34724345 DOI: 10.1111/cts.13162 |
0.12 |
|
2017 |
Brameld KA, Owens TD, Verner E, Venetsanakos E, Bradshaw JM, Phan VT, Tam D, Leung KH, Shu J, LaStant J, Loughhead DG, Karr DE, Gerritsen ME, Goldstein DM, Funk JO. Discovery of the Irreversible Covalent FGFR Inhibitor 8-(3-(4-acryloylpiperazin-1-yl)propyl)-6-(2,6-dichloro-3,5-dimethoxyphenyl)-2-(methylamino)pyrido[2,3-d]pyrimidin-7(8H)-one (PRN1371) for the Treatment of Solid Tumors. Journal of Medicinal Chemistry. PMID 28665128 DOI: 10.1021/acs.jmedchem.7b00360 |
0.109 |
|
2013 |
Padilla F, Bhagirath N, Chen S, Chiao E, Goldstein DM, Hermann JC, Hsu J, Kennedy-Smith JJ, Kuglstatter A, Liao C, Liu W, Lowrie LE, Luk KC, Lynch SM, Menke J, ... ... Owens TD, et al. Pyrrolopyrazines as selective spleen tyrosine kinase inhibitors. Journal of Medicinal Chemistry. 56: 1677-92. PMID 23350847 DOI: 10.1021/jm301720p |
0.086 |
|
2012 |
Xu D, Kim Y, Postelnek J, Vu MD, Hu DQ, Liao C, Bradshaw M, Hsu J, Zhang J, Pashine A, Srinivasan D, Woods J, Levin A, O'Mahony A, Owens TD, et al. RN486, a selective Bruton's tyrosine kinase inhibitor, abrogates immune hypersensitivity responses and arthritis in rodents. The Journal of Pharmacology and Experimental Therapeutics. 341: 90-103. PMID 22228807 DOI: 10.1124/Jpet.111.187740 |
0.079 |
|
2015 |
Zhong Y, Dong S, Strattan E, Ren L, Butchar JP, Thornton K, Mishra A, Porcu P, Bradshaw JM, Bisconte A, Owens TD, Verner E, Brameld KA, Funk JO, Hill RJ, et al. Targeting interleukin-2-inducible T-cell kinase (ITK) and resting lymphocyte kinase (RLK) using a novel covalent inhibitor PRN694. The Journal of Biological Chemistry. 290: 5960-78. PMID 25593320 DOI: 10.1074/Jbc.M114.614891 |
0.073 |
|
2018 |
Basler M, Lindstrom MM, LaStant JJ, Bradshaw JM, Owens TD, Schmidt C, Maurits E, Tsu C, Overkleeft HS, Kirk CJ, Langrish CL, Groettrup M. Co-inhibition of immunoproteasome subunits LMP2 and LMP7 is required to block autoimmunity. Embo Reports. PMID 30279279 DOI: 10.15252/embr.201846512 |
0.06 |
|
2022 |
Owens TD, Brameld KA, Verner EJ, Ton T, Li X, Zhu J, Masjedizadeh MR, Bradshaw JM, Hill RJ, Tam D, Bisconte A, Kim EO, Francesco M, Xing Y, Shu J, et al. Discovery of Reversible Covalent Bruton's Tyrosine Kinase Inhibitors PRN473 and PRN1008 (Rilzabrutinib). Journal of Medicinal Chemistry. PMID 35302767 DOI: 10.1021/acs.jmedchem.1c01170 |
0.06 |
|
2017 |
Venetsanakos E, Brameld KA, Phan VT, Verner E, Owens TD, Xing Y, Tam D, LaStant J, Leung K, Karr DE, Hill RJ, Gerritsen ME, Goldstein DM, Funk JO, Bradshaw JM. The irreversible covalent fibroblast growth factor receptor inhibitor PRN1371 exhibits sustained inhibition of FGFR after drug clearance. Molecular Cancer Therapeutics. PMID 28978721 DOI: 10.1158/1535-7163.MCT-17-0309 |
0.058 |
|
2015 |
Bradshaw JM, McFarland JM, Paavilainen VO, Bisconte A, Tam D, Phan VT, Romanov S, Finkle D, Shu J, Patel V, Ton T, Li X, Loughhead DG, Nunn PA, Karr DE, ... ... Owens TD, et al. Prolonged and tunable residence time using reversible covalent kinase inhibitors. Nature Chemical Biology. 11: 525-31. PMID 26006010 DOI: 10.1038/Nchembio.1817 |
0.056 |
|
2021 |
Langrish CL, Bradshaw JM, Francesco MR, Owens TD, Xing Y, Shu J, LaStant J, Bisconte A, Outerbridge C, White SD, Hill RJ, Brameld KA, Goldstein DM, Nunn PA. Preclinical Efficacy and Anti-Inflammatory Mechanisms of Action of the Bruton Tyrosine Kinase Inhibitor Rilzabrutinib for Immune-Mediated Disease. Journal of Immunology (Baltimore, Md. : 1950). PMID 33674445 DOI: 10.4049/jimmunol.2001130 |
0.056 |
|
2015 |
Hill R, Bradshaw J, Bisconte A, Tam D, Owens T, Brameld K, Smith P, Funk J, Goldstein D, Nunn P. THU0068 Preclinical Characterization of PRN1008, a Novel Reversible Covalent Inhibitor of BTK that Shows Efficacy in a RAT Model of Collagen-Induced Arthritis Annals of the Rheumatic Diseases. 74: 216.2-217. DOI: 10.1136/annrheumdis-2015-eular.3641 |
0.05 |
|
2012 |
Lou Y, Owens TD, Kuglstatter A, Kondru RK, Goldstein DM. Bruton's tyrosine kinase inhibitors: approaches to potent and selective inhibition, preclinical and clinical evaluation for inflammatory diseases and B cell malignancies. Journal of Medicinal Chemistry. 55: 4539-50. PMID 22394077 DOI: 10.1021/jm300035p |
0.049 |
|
2022 |
Modrowski CA, Sheerin KM, Owens T, Pine SM, Shea LM, Frazier E, Lowenhaupt E. Piloting an Evidence-Based Assessment Protocol for Incarcerated Adolescents. Evidence-Based Practice in Child and Adolescent Mental Health. 8: 525-540. PMID 38144516 DOI: 10.1080/23794925.2022.2051216 |
0.048 |
|
2015 |
Cho HS, Shin HM, Haberstock-Debic H, Xing Y, Owens TD, Funk JO, Hill RJ, Bradshaw JM, Berg LJ. A Small Molecule Inhibitor of ITK and RLK Impairs Th1 Differentiation and Prevents Colitis Disease Progression. Journal of Immunology (Baltimore, Md. : 1950). PMID 26466958 DOI: 10.4049/Jimmunol.1501828 |
0.047 |
|
1997 |
Blinkova A, Burkart MF, Owens TD, Walker JR. Conservation of the Escherichia coli dnaX programmed ribosomal frameshift signal in Salmonella typhimurium. Journal of Bacteriology. 179: 4438-42. PMID 9209069 DOI: 10.1128/Jb.179.13.4438-4442.1997 |
0.036 |
|
2021 |
Fitzgerald M, Owens T, Moore J, Goldberg A, Lowenhaupt E, Barron C. Development of a Multi-Session Curriculum Addressing Domestic Minor Sex Trafficking for High-Risk Male Youth. Journal of Child Sexual Abuse. 1-17. PMID 34296663 DOI: 10.1080/10538712.2021.1937427 |
0.033 |
|
2020 |
Moore J, Fitzgerald M, Owens T, Slingsby B, Barron C, Goldberg A. Domestic Minor Sex Trafficking: A Case Series of Male Pediatric Patients. Journal of Interpersonal Violence. 886260519900323. PMID 31948332 DOI: 10.1177/0886260519900323 |
0.017 |
|
1935 |
Owens TD. Current Harmonics in Nonlinear Resistance Circuits Transactions of the American Institute of Electrical Engineers. 54: 1055-1057. DOI: 10.1109/T-AIEE.1935.5056868 |
0.01 |
|
Hide low-probability matches. |