Year |
Citation |
Score |
2022 |
Beshore DC, Haidle AM, Arasappan A, Lim YH, Raheem I, Roecker AJ, Shockley SE, Simov V. Building a Culture of Medicinal Chemistry Knowledge Sharing. Journal of Medicinal Chemistry. PMID 35192762 DOI: 10.1021/acs.jmedchem.1c02144 |
0.546 |
|
2016 |
Beshore DC, Johnson AW, DiPardo RM, Pitts DR, Cofre V, Kuduk SD. 2,5-Disubstituted Pyrazolo[4,3-c]cinnolin-3-ones Journal of Heterocyclic Chemistry. 54: 1558-1571. DOI: 10.1002/Jhet.2744 |
0.35 |
|
2010 |
Beshore DC, DiPardo RM, Kuduk SD. Preparation of 2,4,5-trisubstituted pyrazolo[4,3-c]quinolin-3-ones Tetrahedron Letters. 51: 970-973. DOI: 10.1016/J.Tetlet.2009.12.054 |
0.32 |
|
2009 |
Smith AB, Atasoylu O, Beshore DC. Construction of 5,6-Ring Fused 2-Pyridones: An Effective Annulation Tactic Achieved in Water. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 2009: 2643-2646. PMID 20634903 DOI: 10.1055/S-0029-1217749 |
0.563 |
|
2008 |
Beshore DC, Smith AB. The lyconadins: enantioselective total syntheses of (+)-lyconadin A and (-)-lyconadin B. Journal of the American Chemical Society. 130: 13778-89. PMID 18798629 DOI: 10.1021/Ja804939R |
0.314 |
|
2002 |
Bell IM, Gallicchio SN, Abrams M, Beese LS, Beshore DC, Bhimnathwala H, Bogusky MJ, Buser CA, Culberson JC, Davide J, Ellis-Hutchings M, Fernandes C, Gibbs JB, Graham SL, Hamilton KA, et al. 3-Aminopyrrolidinone farnesyltransferase inhibitors: design of macrocyclic compounds with improved pharmacokinetics and excellent cell potency. Journal of Medicinal Chemistry. 45: 2388-409. PMID 12036349 DOI: 10.1021/Jm010531D |
0.308 |
|
2001 |
Bell IM, Gallicchio SN, Abrams M, Beshore DC, Buser CA, Culberson JC, Davide J, Ellis-Hutchings M, Fernandes C, Gibbs JB, Graham SL, Hartman GD, Heimbrook DC, Homnick CF, Huff JR, et al. Design and biological activity of (S)-4-(5-([1-(3-chlorobenzyl)-2-oxopyrrolidin-3-ylamino]methyl)imidazol-1-ylmethyl)benzonitrile, a 3-aminopyrrolidinone farnesyltransferase inhibitor with excellent cell potency. Journal of Medicinal Chemistry. 44: 2933-49. PMID 11520202 DOI: 10.1021/Jm010156P |
0.306 |
|
2001 |
Beshore DC, Bell IM, Dinsmore CJ, Homnick CF, Culberson JC, Robinson RG, Fernandes C, Walsh ES, Abrams MT, Bhimnathwala HG, Davide JP, Ellis-Hutchings MS, Huber HA, Koblan KS, Buser CA, et al. Evaluation of amino acid-based linkers in potent macrocyclic inhibitors of farnesyl-protein transferase. Bioorganic & Medicinal Chemistry Letters. 11: 1817-21. PMID 11459639 DOI: 10.1016/S0960-894X(01)00340-7 |
0.323 |
|
2000 |
Bell IM, Beshore DC, Gallicchio SN, Williams TM. Efficient synthesis of 1-heterocyclic-3-aminopyrrolidinones Tetrahedron Letters. 41: 1141-1145. DOI: 10.1016/S0040-4039(99)02282-0 |
0.343 |
|
2000 |
Beshore DC, Dinsmore CJ. Efficient synthesis of unsymmetrical 1,4-disubstituted-2,3-diketopiperazines via tandem reductive amination-cyclization Tetrahedron Letters. 41: 8735-8739. DOI: 10.1016/S0040-4039(00)01565-3 |
0.343 |
|
Low-probability matches (unlikely to be authored by this person) |
2014 |
Kuduk SD, Di Marco CN, Saffold JR, Ray WJ, Ma L, Wittmann M, Koeplinger KA, Thompson CD, Hartman GD, Bilodeau MT, Beshore DC. Identification of a methoxynaphthalene scaffold as a core replacement in quinolizidinone amide M(1) positive allosteric modulators. Bioorganic & Medicinal Chemistry Letters. 24: 1417-20. PMID 24485781 DOI: 10.1016/J.Bmcl.2014.01.012 |
0.3 |
|
2018 |
Salter R, Beshore DC, Colletti SL, Evans L, Gong Y, Helmy R, Liu Y, Maciolek CM, Martin G, Pajkovic N, Phipps R, Small J, Steele J, de Vries R, Williams H, et al. Microbial Biotransformation - An Important Tool for the Study of Drug Metabolism. Xenobiotica; the Fate of Foreign Compounds in Biological Systems. 1-38. PMID 30118378 DOI: 10.1080/00498254.2018.1512018 |
0.299 |
|
2006 |
Trotter BW, Nanda KK, Kett NR, Regan CP, Lynch JJ, Stump GL, Kiss L, Wang J, Spencer RH, Kane SA, White RB, Zhang R, Anderson KD, Liverton NJ, McIntyre CJ, ... Beshore DC, et al. Design and synthesis of novel isoquinoline-3-nitriles as orally bioavailable Kv1.5 antagonists for the treatment of atrial fibrillation. Journal of Medicinal Chemistry. 49: 6954-7. PMID 17125248 DOI: 10.1021/Jm060927V |
0.298 |
|
2002 |
Beshore DC, Dinsmore CJ. Preparation of substituted piperazinones via tandem reductive amination-(N,N'-acyl transfer)-cyclization. Organic Letters. 4: 1201-4. PMID 11922818 DOI: 10.1021/Ol025644L |
0.297 |
|
2002 |
Dinsmore CJ, Beshore DC. Syntheses and transformations of piperazinone rings. A review Organic Preparations and Procedures International. 34: 367-404. DOI: 10.1080/00304940209458075 |
0.293 |
|
2020 |
Yu W, Liu J, Yu Y, Zhang V, Clausen D, Kelly J, Wolkenberg S, Beshore D, Duffy JL, Chang CC, Myers RW, Klein DJ, Fells J, Holloway K, Wu J, et al. Discovery of ethyl ketone-based HDACs 1, 2, and 3 selective inhibitors for HIV latency reactivation. Bioorganic & Medicinal Chemistry Letters. 127197. PMID 32331932 DOI: 10.1016/J.Bmcl.2020.127197 |
0.29 |
|
2002 |
Dinsmore CJ, Beshore DC. Recent advances in the synthesis of diketopiperazines Tetrahedron. 58: 3297-3312. DOI: 10.1016/S0040-4020(02)00239-9 |
0.288 |
|
2014 |
Kuduk SD, Beshore DC. SAR studies on carboxylic acid series M(1) selective positive allosteric modulators (PAMs). Current Topics in Medicinal Chemistry. 14: 1738-54. PMID 25176125 DOI: 10.2174/1568026614666140826120224 |
0.284 |
|
2010 |
Kuduk SD, DiPardo RM, Beshore DC, Ray WJ, Ma L, Wittmann M, Seager MA, Koeplinger KA, Thompson CD, Hartman GD, Bilodeau MT. Hydroxy cycloalkyl fused pyridone carboxylic acid M(1) positive allosteric modulators. Bioorganic & Medicinal Chemistry Letters. 20: 2538-41. PMID 20346667 DOI: 10.1016/J.Bmcl.2010.02.095 |
0.284 |
|
2018 |
Beshore DC, N Di Marco C, Chang RK, Greshock TJ, Ma L, Wittmann M, Seager MA, Koeplinger KA, Thompson CD, Fuerst J, Hartman GD, Bilodeau MT, Ray WJ, Kuduk SD. MK-7622: A First-in-Class M Positive Allosteric Modulator Development Candidate. Acs Medicinal Chemistry Letters. 9: 652-656. PMID 30034595 DOI: 10.1021/Acsmedchemlett.8B00095 |
0.282 |
|
2017 |
Sanders JM, Beshore DC, Culberson JC, Fells JI, Imbriglio JE, Gunaydin H, Haidle AM, Labroli M, Mattioni BE, Sciammetta N, Shipe WD, Sheridan RP, Suen LM, Verras A, Walji AM, et al. Informing the selection of screening hit series with in silico absorption, distribution, metabolism, excretion, and toxicity profiles. Journal of Medicinal Chemistry. PMID 28418656 DOI: 10.1021/Acs.Jmedchem.6B01577 |
0.271 |
|
2003 |
Beshore DC, Dinsmore CJ. Preparation of ethyl 5-iodo-1H-indole-2-carboxylate Synthetic Communications. 33: 2423-2427. DOI: 10.1081/Scc-120021830 |
0.269 |
|
2010 |
Beshore DC, Liverton NJ, McIntyre CJ, Claiborne CF, Libby B, Culberson JC, Salata JJ, Regan CP, Lynch JJ, Kiss L, Spencer RH, Kane SA, White RB, Yeh S, Hartman GD, et al. Discovery of triarylethanolamine inhibitors of the Kv1.5 potassium channel. Bioorganic & Medicinal Chemistry Letters. 20: 2493-6. PMID 20304642 DOI: 10.1016/J.Bmcl.2010.03.005 |
0.267 |
|
2018 |
Uslaner JM, Kuduk SD, Wittmann M, Lange HS, Fox SV, Min C, Pajkovic N, Harris D, Cilissen C, Mahon C, Mostoller K, Warrington S, Beshore DC. Preclinical to Human Translational Pharmacology of the Novel MPositive Allosteric Modulator MK-7622. The Journal of Pharmacology and Experimental Therapeutics. PMID 29563325 DOI: 10.1124/Jpet.117.245894 |
0.261 |
|
2012 |
Kuduk SD, Beshore DC. Novel M(1) allosteric ligands: a patent review. Expert Opinion On Therapeutic Patents. 22: 1385-98. PMID 23092292 DOI: 10.1517/13543776.2012.731395 |
0.255 |
|
2008 |
Regan CP, Kiss L, Stump GL, McIntyre CJ, Beshore DC, Liverton NJ, Dinsmore CJ, Lynch JJ. Atrial antifibrillatory effects of structurally distinct IKur blockers 3-[(dimethylamino)methyl]-6-methoxy-2-methyl-4-phenylisoquinolin-1(2H)-one and 2-phenyl-1,1-dipyridin-3-yl-2-pyrrolidin-1-yl-ethanol in dogs with underlying heart failure. The Journal of Pharmacology and Experimental Therapeutics. 324: 322-30. PMID 17967939 DOI: 10.1124/Jpet.107.127654 |
0.25 |
|
2017 |
Homsher MF, Beshore DC, Cassaday J, Squadroni B, Mohammed E, Hartnett M, Day S, Ma L, Pechter D, Smith MD, Monsma F, Zuck P, Finley MF, Uebele VN, Hermes JD. High-Throughput Agonist Shift Assay Development for the Analysis of M1-Positive Allosteric Modulators. Slas Discovery. 2472555217705373. PMID 28426939 DOI: 10.1177/2472555217705373 |
0.159 |
|
2021 |
Beshore DC, Adam GC, Barnard RJO, Burlein C, Gallicchio SN, Holloway MK, Krosky D, Lemaire W, Myers RW, Patel S, Plotkin MA, Powell DA, Rada V, Cox CD, Coleman PJ, et al. Redefining the Histone Deacetylase Inhibitor Pharmacophore: High Potency with No Zinc Cofactor Interaction. Acs Medicinal Chemistry Letters. 12: 540-547. PMID 33854701 DOI: 10.1021/acsmedchemlett.1c00074 |
0.113 |
|
2023 |
Kleiner VA, O Fischmann T, Howe JA, Beshore DC, Eddins MJ, Hou Y, Mayhood T, Klein D, Nahas DD, Lucas BJ, Xi H, Murray E, Ma DY, Getty K, Fearns R. Conserved allosteric inhibitory site on the respiratory syncytial virus and human metapneumovirus RNA-dependent RNA polymerases. Communications Biology. 6: 649. PMID 37337079 DOI: 10.1038/s42003-023-04990-0 |
0.085 |
|
2022 |
Moore KP, Schwaid AG, Tudor M, Park S, Beshore DC, Converso A, Shipe WD, Anand R, Lan P, Moningka R, Rothman DM, Sun W, Chi A, Cornella-Taracido I, Adam GC, et al. A Phenotypic Screen Identifies Potent DPP9 Inhibitors Capable of Killing HIV-1 Infected Cells. Acs Chemical Biology. PMID 36044633 DOI: 10.1021/acschembio.2c00515 |
0.085 |
|
2007 |
Beshore DC, Smith AB. Total syntheses of (+)-lyconadin A and (-)-lyconadin B. Journal of the American Chemical Society. 129: 4148-9. PMID 17367142 DOI: 10.1021/ja070336+ |
0.063 |
|
Hide low-probability matches. |