Year |
Citation |
Score |
2020 |
Escobar RA, Johannes JW. A Unified and Practical Method for Carbon-Heteroatom Cross-Coupling using Nickel/Photo Dual Catalysis. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32065838 DOI: 10.1002/Chem.202000052 |
0.313 |
|
2020 |
Howard RT, Hemsley P, Petteruti P, Saunders CN, Molina Bermejo JA, Scott JS, Johannes JW, Tate EW. Structure-guided design and in-cell target profiling of a cell-active target engagement probe for PARP inhibitors. Acs Chemical Biology. PMID 32017532 DOI: 10.1021/Acschembio.9B00963 |
0.371 |
|
2018 |
Tron AE, Belmonte MA, Adam A, Aquila BM, Boise LH, Chiarparin E, Cidado J, Embrey KJ, Gangl E, Gibbons FD, Gregory GP, Hargreaves D, Hendricks JA, Johannes JW, Johnstone RW, et al. Discovery of Mcl-1-specific inhibitor AZD5991 and preclinical activity in multiple myeloma and acute myeloid leukemia. Nature Communications. 9: 5341. PMID 30559424 DOI: 10.1038/S41467-018-07551-W |
0.331 |
|
2018 |
Wang Z, Grosskurth SE, Cheung T, Petteruti P, Zhang J, Wang X, Wang W, Gharahdaghi F, Wu J, Su N, Howard RT, Mayo M, Widzowski D, Scott DA, Johannes JW, et al. Pharmacological inhibition of PARP6 triggers multipolar spindle formation and elicits therapeutic effects in breast cancer. Cancer Research. PMID 30297535 DOI: 10.1158/0008-5472.Can-18-1362 |
0.376 |
|
2018 |
Gingipalli L, Block MH, Bao L, Cooke E, Dakin LA, Denz CR, Ferguson AD, Johannes JW, Larsen NA, Lyne PD, Pontz TW, Wang T, Wu X, Wu A, Zhang HJ, et al. Discovery of 2,6-disubstituted pyrazine derivatives as inhibitors of CK2 and PIM kinases. Bioorganic & Medicinal Chemistry Letters. PMID 29559278 DOI: 10.1016/J.Bmcl.2018.03.018 |
0.388 |
|
2018 |
Leo E, Johannes J, Illuzzi G, Zhang A, Hemsley P, Bista MJ, Orme JP, Talbot VA, Narvaez AJ, Underwood E, Pike A, Nikkila JK, Riches L, Sweeney S, Gustafsson F, et al. Abstract LB-273: A head-to-head comparison of the properties of five clinical PARP inhibitors identifies new insights that can explain both the observed clinical efficacy and safety profiles Cancer Research. 78. DOI: 10.1158/1538-7445.Am2018-Lb-273 |
0.326 |
|
2018 |
Konev MO, McTeague TA, Johannes JW. Nickel-Catalyzed Photoredox-Mediated Cross-Coupling of Aryl Electrophiles and Aryl Azides Acs Catalysis. 8: 9120-9124. DOI: 10.1021/Acscatal.8B02954 |
0.341 |
|
2017 |
Johannes J, Denz CR, Su N, Wu A, Impastato AC, Mlynarski S, Varnes JG, Prince DB, Cidado J, Gao N, Haddrick M, Jones NH, Li S, Li X, Liu Y, et al. Structure Based Design of Selective Non-covalent CDK12 Inhibitors. Chemmedchem. PMID 29266803 DOI: 10.1002/Cmdc.201700695 |
0.394 |
|
2017 |
Johannes JW, Bates S, Beigie C, Belmonte MA, Breen J, Cao S, Centrella PA, Clark MA, Cuozzo JW, Dumelin CE, Ferguson AD, Habeshian S, Hargreaves D, Joubran C, Kazmirski S, et al. Structure Based Design of Non-Natural Peptidic Macrocyclic Mcl-1 Inhibitors. Acs Medicinal Chemistry Letters. 8: 239-244. PMID 28197319 DOI: 10.1021/Acsmedchemlett.6B00464 |
0.346 |
|
2017 |
Hird AW, Secrist JP, Adam A, Belmonte MA, Gangl E, Gibbons F, Hargreaves D, Johannes JW, Kazmirski SL, Kettle JG, Kurtz SE, Lamb ML, Packer MJ, Peng B, Stewart CR, et al. Abstract DDT01-02: AZD5991: A potent and selective macrocyclic inhibitor of Mcl-1 for treatment of hematologic cancers Cancer Research. 77. DOI: 10.1158/1538-7445.Am2017-Ddt01-02 |
0.342 |
|
2016 |
Gu C, Lamb ML, Johannes JW, Sylvester MA, Eisman MS, Harrison RA, Hu H, Kazmirski S, Mikule K, Peng B, Su N, Wang W, Ye Q, Zheng X, Lyne PD, et al. Modulating the strength of hydrogen bond acceptors to achieve low Caco2 efflux for oral bioavailability of PARP inhibitors blocking centrosome clustering. Bioorganic & Medicinal Chemistry Letters. PMID 27578247 DOI: 10.1016/J.Bmcl.2016.08.030 |
0.31 |
|
2016 |
Oderinde MS, Jones NH, Juneau A, Frenette M, Aquila B, Tentarelli S, Robbins DW, Johannes JW. Highly Chemoselective Iridium Photoredox and Nickel Catalysis for the Cross-Coupling of Primary Aryl Amines with Aryl Halides. Angewandte Chemie (International Ed. in English). PMID 27436532 DOI: 10.1002/Anie.201604429 |
0.325 |
|
2016 |
Oderinde MS, Frenette M, Robbins DW, Aquila B, Johannes JW. Photoredox Mediated Nickel Catalyzed Cross-Coupling of Thiols With Aryl and Heteroaryl Iodides via Thiyl Radicals. Journal of the American Chemical Society. PMID 26840123 DOI: 10.1021/Jacs.5B11244 |
0.321 |
|
2016 |
Oderinde MS, Jones NH, Juneau A, Frenette M, Aquila B, Tentarelli S, Robbins DW, Johannes JW. Back Cover: Highly Chemoselective Iridium Photoredox and Nickel Catalysis for the Cross-Coupling of Primary Aryl Amines with Aryl Halides (Angew. Chem. Int. Ed. 42/2016) Angewandte Chemie International Edition. 55: 13350-13350. DOI: 10.1002/Anie.201607767 |
0.319 |
|
2016 |
Oderinde MS, Jones NH, Juneau A, Frenette M, Aquila B, Tentarelli S, Robbins DW, Johannes JW. Rücktitelbild: Highly Chemoselective Iridium Photoredox and Nickel Catalysis for the Cross-Coupling of Primary Aryl Amines with Aryl Halides (Angew. Chem. 42/2016) Angewandte Chemie. 128: 13546-13546. DOI: 10.1002/Ange.201607767 |
0.317 |
|
2015 |
Johannes JW, Almeida L, Daly K, Ferguson AD, Grosskurth SE, Guan H, Howard T, Ioannidis S, Kazmirski S, Lamb ML, Larsen NA, Lyne PD, Mikule K, Ogoe C, Peng B, et al. Discovery of AZ0108, an orally bioavailable phthalazinone PARP inhibitor that blocks centrosome clustering. Bioorganic & Medicinal Chemistry Letters. PMID 26546219 DOI: 10.1016/J.Bmcl.2015.10.079 |
0.366 |
|
2015 |
Johannes JW, Almeida L, Barlaam B, Boriack-Sjodin PA, Casella R, Croft RA, Dishington AP, Gingipalli L, Gu C, Hawkins JL, Holmes JL, Howard T, Huang J, Ioannidis S, Kazmirski S, et al. Pyrimidinone nicotinamide mimetics as selective tankyrase and wnt pathway inhibitors suitable for in vivo pharmacology. Acs Medicinal Chemistry Letters. 6: 254-9. PMID 25815142 DOI: 10.1021/Ml5003663 |
0.372 |
|
2014 |
Johannes JW, Chuaqui C, Cowen S, Devereaux E, Gingipalli L, Molina A, Wang T, Whitston D, Wu X, Zhang HJ, Zinda M. Discovery of 6-aryl-azabenzimidazoles that inhibit the TBK1/IKK-ε kinases. Bioorganic & Medicinal Chemistry Letters. 24: 1138-43. PMID 24462666 DOI: 10.1016/J.Bmcl.2013.12.123 |
0.409 |
|
2013 |
Vasbinder MM, Aquila B, Augustin M, Chen H, Cheung T, Cook D, Drew L, Fauber BP, Glossop S, Grondine M, Hennessy E, Johannes J, Lee S, Lyne P, Mörtl M, et al. Discovery and optimization of a novel series of potent mutant B-Raf(V600E) selective kinase inhibitors. Journal of Medicinal Chemistry. 56: 1996-2015. PMID 23398453 DOI: 10.1021/Jm301658D |
0.357 |
|
2012 |
Wang T, Block MA, Cowen S, Davies AM, Devereaux E, Gingipalli L, Johannes J, Larsen NA, Su Q, Tucker JA, Whitston D, Wu J, Zhang HJ, Zinda M, Chuaqui C. Discovery of azabenzimidazole derivatives as potent, selective inhibitors of TBK1/IKKε kinases. Bioorganic & Medicinal Chemistry Letters. 22: 2063-9. PMID 22305584 DOI: 10.1016/J.Bmcl.2012.01.018 |
0.395 |
|
2011 |
Cooke E, Alimzhanov M, Almeida L, Bao L, Bedian V, Brown J, Deng C, Denz C, Gingipalli L, Johannes J, Kazmirski S, Lamb M, Liu Z, Racicot V, Su N, et al. Abstract 5196: The discovery of small molecule inhibitors of Tankyrases 1 and 2, which modulate Axin homeostasis and inhibit Wnt signalingin vivo Cancer Research. 71: 5196-5196. DOI: 10.1158/1538-7445.Am2011-5196 |
0.351 |
|
2005 |
Johannes JW, Wenglowsky S, Kishi Y. Biomimetic macrocycle-forming Diels-Alder reaction of an iminium dienophile: synthetic studies directed toward gymnodimine. Organic Letters. 7: 3997-4000. PMID 16119951 DOI: 10.1021/Ol051553N |
0.412 |
|
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