Year |
Citation |
Score |
2022 |
Mitachi K, Mingle D, Effah W, Sánchez-Ruiz A, Hevener KE, Narayanan R, Clemons WM, Sarabia F, Kurosu M. Concise Synthesis of Tunicamycin V and Discovery of a Cytostatic DPAGT1 Inhibitor. Angewandte Chemie (International Ed. in English). e202203225. PMID 35594368 DOI: 10.1002/anie.202203225 |
0.606 |
|
2020 |
Mitachi K, Kansal RG, Hevener KE, Gillman CD, Hussain SM, Yun HG, Miranda-Carboni GA, Glazer ES, Clemons WM, Kurosu M. DPAGT1 Inhibitors of Capuramycin Analogues and Their Antimigratory Activities of Solid Tumors. Journal of Medicinal Chemistry. PMID 32886511 DOI: 10.1021/Acs.Jmedchem.0C00545 |
0.612 |
|
2019 |
Mitachi K, Yun HG, Gillman CD, Skorupinska-Tudek K, Swiezewska E, Clemons WM, Kurosu M. Substrate Tolerance of Bacterial Glycosyltransferase MurG: Novel Fluorescence-based Assays. Acs Infectious Diseases. PMID 31769280 DOI: 10.1021/Acsinfecdis.9B00242 |
0.616 |
|
2019 |
Mitachi K, Kurosu SM, Gillman CD, Yun HG, Clemons WM, Kurosu M. A practical synthesis of a novel DPAGT1 inhibitor, aminouridyl phenoxypiperidinbenzyl butanamide (APPB) for in vivo studies. Methodsx. 6: 2305-2321. PMID 31667130 DOI: 10.1016/J.Mex.2019.09.031 |
0.651 |
|
2019 |
Mitachi K, Kurosu SM, Eslamimehr S, Lemieux MR, Ishizaki Y, Clemons WM, Kurosu M. Semisynthesis of an Anticancer DPAGT1 Inhibitor from a Muraymycin Biosynthetic Intermediate. Organic Letters. 21: 876-879. PMID 30698984 DOI: 10.1021/Acs.Orglett.8B03716 |
0.634 |
|
2018 |
Lemieux MR, Siricilla S, Mitachi K, Eslamimehr S, Wang Y, Yang D, Pressly JD, Kong Y, Park F, Franzblau SG, Kurosu M. An antimycobacterial pleuromutilin analogue effective against dormant bacilli. Bioorganic & Medicinal Chemistry. PMID 30145051 DOI: 10.1016/J.Bmc.2018.07.034 |
0.314 |
|
2018 |
Mitachi K, Yun HG, Kurosu SM, Eslamimehr S, Lemieux MR, Klaić L, Clemons WM, Kurosu M. Novel FR-900493 Analogues That Inhibit the Outgrowth ofSpores. Acs Omega. 3: 1726-1739. PMID 29503973 DOI: 10.1021/acsomega.7b01740 |
0.597 |
|
2016 |
Yang D, Ding F, Mitachi K, Kurosu M, Lee RE, Kong Y. A Fluorescent Probe for Detecting Mycobacterium tuberculosis and Identifying Genes Critical for Cell Entry. Frontiers in Microbiology. 7: 2021. PMID 28066347 DOI: 10.3389/Fmicb.2016.02021 |
0.309 |
|
2016 |
Mitachi K, Aleiwi BA, Schneider CM, Siricilla S, Kurosu M. Stereocontrolled Total Synthesis of Muraymycin D1 Having a Dual Mode of Action against Mycobacterium tuberculosis. Journal of the American Chemical Society. PMID 27617631 DOI: 10.1021/Jacs.6B07395 |
0.395 |
|
2016 |
Mitachi K, Siricilla S, Yang D, Kong Y, Skorupinska-Tudek K, Swiezewska E, Franzblau SG, Kurosu M. Fluorescence-based assay for polyprenyl phosphate-GlcNAc-1-phosphate transferase (WecA) and identification of novel antimycobacterial WecA inhibitors. Analytical Biochemistry. PMID 27530653 DOI: 10.1016/J.Ab.2016.08.008 |
0.36 |
|
2016 |
Mitachi K, Kurosu YE, Hazlett BT, Kurosu M. Oxyma-based phosphates for racemization-free peptide segment couplings. Journal of Peptide Science : An Official Publication of the European Peptide Society. 22: 186-91. PMID 26856693 DOI: 10.1002/Psc.2859 |
0.321 |
|
2015 |
Mitachi K, Siricilla S, Klaic L, Clemons WM, Kurosu M. Chemoenzymatic syntheses of water-soluble lipid I fluorescent probes. Tetrahedron Letters. 56: 3441-3446. PMID 26190869 DOI: 10.1016/J.Tetlet.2015.01.044 |
0.633 |
|
2015 |
Siricilla S, Mitachi K, Wan B, Franzblau SG, Kurosu M. Discovery of a capuramycin analog that kills nonreplicating Mycobacterium tuberculosis and its synergistic effects with translocase I inhibitors. The Journal of Antibiotics. 68: 271-8. PMID 25269459 DOI: 10.1038/Ja.2014.133 |
0.346 |
|
2015 |
Mitachi K, Siricilla S, Klai? L, Clemons WM, Kurosu M. Chemoenzymatic syntheses of water-soluble lipid i fluorescent probes This Letter is dedicated to the memory of Professor Harry H. Wasserman, an inspirational scientist Tetrahedron Letters. 56: 3441-3446. DOI: 10.1016/j.tetlet.2015.01.044 |
0.555 |
|
2014 |
Siricilla S, Mitachi K, Skorupinska-Tudek K, Swiezewska E, Kurosu M. Biosynthesis of a water-soluble lipid I analogue and a convenient assay for translocase I. Analytical Biochemistry. 461: 36-45. PMID 24939461 DOI: 10.1016/J.Ab.2014.05.018 |
0.391 |
|
2014 |
Mitachi K, Mohan P, Siricilla S, Kurosu M. One-pot protection-glycosylation reactions for synthesis of lipid II analogues. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 4554-8. PMID 24623584 DOI: 10.1002/Chem.201400307 |
0.35 |
|
2013 |
Wang Y, Siricilla S, Aleiwi BA, Kurosu M. Improved synthesis of capuramycin and its analogues Chemistry - a European Journal. 19: 13847-13858. PMID 24014478 DOI: 10.1002/Chem.201302389 |
0.382 |
|
2013 |
Aleiwi BA, Mitachi K, Kurosu M. Mild and convenient N-formylation protocol in water-containing solvents. Tetrahedron Letters. 54: 2077-2081. PMID 23908559 DOI: 10.1016/J.Tetlet.2013.02.013 |
0.36 |
|
2012 |
Wang Y, Kurosu M. A new protecting group and linker for uridine ureido nitrogen. Tetrahedron. 68: 4797-4804. PMID 22711936 DOI: 10.1016/J.Tet.2012.03.121 |
0.321 |
|
2012 |
Wang Q, Wang Y, Kurosu M. A new oxyma derivative for nonracemizable amide-forming reactions in water Organic Letters. 14: 3372-3375. PMID 22697488 DOI: 10.1021/Ol3013556 |
0.32 |
|
2012 |
Aleiwi BA, Schneider CM, Kurosu M. Synthesis of ureidomuraymycidine derivatives for structure-activity relationship studies of muraymycins Journal of Organic Chemistry. 77: 3859-3867. PMID 22458337 DOI: 10.1021/Jo300205B |
0.312 |
|
2012 |
Debnath J, Siricilla S, Wan B, Crick DC, Lenaerts AJ, Franzblau SG, Kurosu M. Discovery of selective menaquinone biosynthesis inhibitors against Mycobacterium tuberculosis. Journal of Medicinal Chemistry. 55: 3739-55. PMID 22449052 DOI: 10.1021/Jm201608G |
0.376 |
|
2010 |
Kurosu M, Li K. MILD AND SELECTIVE O-GLYCOSYLATIONS OF PRIMARY ALCOHOLS WITH THE THIOGLUCOSAMINIDE DERIVATIVE PROMOTED BY N-IODOSUCCINIMIDE AND HBF(4)-ADOSROBED ON SILICA GEL. Heterocycles. 80: 115-123. PMID 23239901 DOI: 10.3987/Com-09-S(S)24 |
0.349 |
|
2009 |
Kurosu M, Li K, Crick DC. Concise synthesis of capuramycin. Organic Letters. 11: 2393-6. PMID 19405507 DOI: 10.1021/Ol900458W |
0.337 |
|
2009 |
Kurosu M, Crick DC. MenA is a promising drug target for developing novel lead molecules to combat Mycobacterium tuberculosis. Medicinal Chemistry (ShāRiqah (United Arab Emirates)). 5: 197-207. PMID 19275719 DOI: 10.2174/157340609787582882 |
0.335 |
|
2009 |
Dhiman RK, Mahapatra S, Slayden RA, Boyne ME, Lenaerts A, Hinshaw JC, Angala SK, Chatterjee D, Biswas K, Narayanasamy P, Kurosu M, Crick DC. Menaquinone synthesis is critical for maintaining mycobacterial viability during exponential growth and recovery from non-replicating persistence. Molecular Microbiology. 72: 85-97. PMID 19220750 DOI: 10.1111/J.1365-2958.2009.06625.X |
0.338 |
|
2009 |
Kurosu M, Li K. Synthetic studies towards the identification of novel capuramycin analogs with mycobactericidal activity Heterocycles. 77: 217-225. DOI: 10.3987/Com-08-S(F)38 |
0.349 |
|
2008 |
Li K, Kurosu M. Synthetic studies on Mycobacterium tuberculosis specific fluorescent Park's nucleotide probe Heterocycles. 76: 455-469. DOI: 10.3987/Com-08-S(N)30 |
0.342 |
|
2007 |
Kurosu M, Narayanasamy P, Biswas K, Dhiman R, Crick DC. Discovery of 1,4-dihydroxy-2-naphthoate [corrected] prenyltransferase inhibitors: new drug leads for multidrug-resistant gram-positive pathogens. Journal of Medicinal Chemistry. 50: 3973-5. PMID 17658779 DOI: 10.1021/Jm070638M |
0.3 |
|
2007 |
Kurosu M, Biswas K, Crick DC. Polymer-supported (2,6-dichloro- 4-alkoxyphenyl)(2,4-dichlorophenyl)methanol: a new linker for solid-phase organic synthesis. Organic Letters. 9: 1141-4. PMID 17311394 DOI: 10.1021/Ol070150F |
0.312 |
|
2007 |
Kurosu M, Narayanasamy P, Crick DC. High-throughput synthesis of substituted hydrazine derivatives Heterocycles. 73: 169-175. DOI: 10.3987/Com-07-S(U)14 |
0.35 |
|
2007 |
Kurosu M, Narayanasamy P, Crick DC. Synthetic studies toward the generation of uridine-amino alcohol-based small optimized libraries Heterocycles. 72: 339-352. DOI: 10.3987/Com-06-S(K)18 |
0.329 |
|
2007 |
Kurosu M, Mahapatra S, Narayanasamy P, Crick DC. Chemoenzymatic synthesis of Park's nucleotide: toward the development of high-throughput screening for MraY inhibitors Tetrahedron Letters. 48: 799-803. DOI: 10.1016/J.Tetlet.2006.11.160 |
0.335 |
|
2006 |
Kurosu M, Kitagawa I. Ganglioside GM3 derivatives with truncated ceramide moiety: Facial synthesis and inhibitory activity against KB cell growth Journal of Carbohydrate Chemistry. 25: 427-439. DOI: 10.1080/07328300600803518 |
0.357 |
|
2006 |
Kurosu M, Crick DC. A novel strategy for oligopeptide synthesis using a polymer-supported ammonium fluoride Tetrahedron Letters. 47: 5325-5328. DOI: 10.1016/J.Tetlet.2006.05.129 |
0.343 |
|
2006 |
Kurosu M, Dey SS, Crick DC. Efficient synthesis of tertiary amines from secondary amines Tetrahedron Letters. 47: 4871-4875. DOI: 10.1016/J.Tetlet.2006.05.038 |
0.355 |
|
2005 |
Kurosu M, Lorca M. Effect of water on Keck's catalytic asymmetric allylations of aldehydes Synlett. 1109-1112. DOI: 10.1055/S-2005-865202 |
0.308 |
|
2004 |
Kurosu M, Lin MH, Kishi Y. Fe/Cr- and Co/Cr-mediated catalytic asymmetric 2-haloallylations of aldehydes. Journal of the American Chemical Society. 126: 12248-9. PMID 15453741 DOI: 10.1021/Ja045557J |
0.459 |
|
2004 |
Kurosu M, Kishi Y. Studies on the total synthesis of batrachotoxin Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry. 62: 1205-1217. DOI: 10.5059/Yukigoseikyokaishi.62.1205 |
0.348 |
|
2004 |
Kurosu M, Porter JR, Foley MA. An efficient synthesis of indane-derived bis(oxazoline) and its application to hetero Diels-Alder reactions on polymer support Tetrahedron Letters. 45: 145-148. DOI: 10.1016/J.Tetlet.2003.10.097 |
0.319 |
|
2001 |
Kurosu M, Lorca M. Highly diastereofacial anti-aldol reaction: Practical synthesis of optically active anti-2-alkyl-3-hydroxycarboxylic acid ester units Journal of Organic Chemistry. 66: 1205-1209. PMID 11312949 DOI: 10.1021/Jo001293H |
0.358 |
|
2001 |
Lorca M, Kurosu M. An efficient amide-forming reaction using tributyltrichloromethylphosphonium chloride Synthetic Communications. 31: 469-473. DOI: 10.1081/Scc-100000572 |
0.303 |
|
2001 |
Lorca M, Kurosu M. A practical synthesis of the lipophilic side chain of the polyoxypeptins Tetrahedron Letters. 42: 2431-2434. DOI: 10.1016/S0040-4039(01)00205-2 |
0.343 |
|
2000 |
Kurosu M. Expeditious amide-forming reactions using thiol esters Tetrahedron Letters. 41: 591-594. DOI: 10.1016/S0040-4039(99)02132-2 |
0.354 |
|
1998 |
Kurosu M, Kishi Y. A Novel Example for Optical Resolution of Racemic Ketones Originating from Batrachotoxin Synthesis. The Journal of Organic Chemistry. 63: 6100-6101. PMID 11672234 DOI: 10.1021/Jo981416M |
0.463 |
|
1998 |
Kurosu M, Marcin LR, Kishi Y. A useful modification of the Garst-Spencer furan annulation: An improved synthesis of 3,4-substituted furans Tetrahedron Letters. 39: 8929-8932. DOI: 10.1016/S0040-4039(98)02017-6 |
0.344 |
|
1998 |
Kurosu M, Kishi Y. Reaction of methylcerium reagent with tertiary amides: Synthesis of saturated and unsaturated ketones from tertiary amides Tetrahedron Letters. 39: 4793-4796. DOI: 10.1016/S0040-4039(98)00959-9 |
0.344 |
|
1994 |
Kobayashi M, Kurosu M, Wang W, Kitagawa I. A Total Synthesis Of Arenastatin A, An Extremely Potent Cytotoxic Depsipeptide, From The Okinawan Marine Sponge Dysidea Arenaria Chemical & Pharmaceutical Bulletin. 42: 2394-2396. DOI: 10.1248/Cpb.42.2394 |
0.351 |
|
1994 |
Kobayashi M, Kurosu M, Ohyabu N, Wang W, Fujii S, Kitagawa I. The Absolute Stereostructure Of Arenastatin A, A Potent Cytotoxic Depsipeptide From The Okinawan Marine Sponge Dysidea Arenaria Chemical & Pharmaceutical Bulletin. 42: 2196-2198. DOI: 10.1248/Cpb.42.2196 |
0.302 |
|
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