| Year |
Citation |
Score |
| 2024 |
Liu C, Zhang M, Zeng L, Wan Y, Dai M. Ten-Step Total Synthesis of (±)-Phaeocaulisin A Enabled by Cyclopropanol Ring-Opening Carbonylation. Journal of the American Chemical Society. PMID 39532298 DOI: 10.1021/jacs.4c12121 |
0.317 |
|
| 2023 |
Jiang B, Dai M. Concise Total Syntheses of the 6-7-5 Hamigeran Natural Products. Journal of the American Chemical Society. 145: 18731-18736. PMID 37603855 DOI: 10.1021/jacs.3c06031 |
0.306 |
|
| 2023 |
Dai JJ, Yin X, Li L, Rivera ME, Wang YC, Dai M. Modular and practical diamination of allenes. Nature Communications. 14: 1774. PMID 36997504 DOI: 10.1038/s41467-023-37345-8 |
0.685 |
|
| 2023 |
Sims HS, Dai M. Palladium-Catalyzed Carbonylations: Application in Complex Natural Product Total Synthesis and Recent Developments. The Journal of Organic Chemistry. PMID 36705327 DOI: 10.1021/acs.joc.2c02746 |
0.309 |
|
| 2022 |
Xu B, Liu C, Dai M. Catalysis-Enabled 13-Step Total Synthesis of (-)-Peyssonnoside A. Journal of the American Chemical Society. 144: 19700-19703. PMID 36279290 DOI: 10.1021/jacs.2c09919 |
0.301 |
|
| 2021 |
Negi V, Yang J, Speyer G, Pulgarin A, Handen A, Zhao J, Tai YY, Tang Y, Culley MK, Yu Q, Forsythe P, Gorelova A, Watson AM, Al Aaraj Y, Satoh T, ... ... Dai M, et al. Computational repurposing of therapeutic small molecules from cancer to pulmonary hypertension. Science Advances. 7: eabh3794. PMID 34669463 DOI: 10.1126/sciadv.abh3794 |
0.574 |
|
| 2021 |
Ma D, Martin BS, Gallagher KS, Saito T, Dai M. One-Carbon Insertion and Polarity Inversion Enabled a Pyrrole Strategy to the Total Syntheses of Pyridine-Containing Alkaloids: Complanadine A and Lycodine. Journal of the American Chemical Society. PMID 34570487 DOI: 10.1021/jacs.1c08626 |
0.752 |
|
| 2021 |
Dai M, Wang YC, Cui C. Flow Chemistry-Enabled Divergent and Enantioselective Total Syntheses of Massarinolin A, Purpurolides B, D, E, 2,3-Deoxypurpurolide C, and Structural Revision of Massarinolin A. Angewandte Chemie (International Ed. in English). PMID 34405497 DOI: 10.1002/anie.202109625 |
0.723 |
|
| 2021 |
Cui C, Dwyer BG, Liu C, Abegg D, Cai ZJ, Hoch DG, Yin X, Qiu N, Liu JQ, Adibekian A, Dai M. Total Synthesis and Target Identification of the Curcusone Diterpenes. Journal of the American Chemical Society. PMID 33705657 DOI: 10.1021/jacs.1c00557 |
0.78 |
|
| 2021 |
Raffa N, Won TH, Sukowaty A, Candor K, Cui C, Halder S, Dai M, Landero-Figueroa JA, Schroeder FC, Keller NP. Dual-purpose isocyanides produced by contribute to cellular copper sufficiency and exhibit antimicrobial activity. Proceedings of the National Academy of Sciences of the United States of America. 118. PMID 33593906 DOI: 10.1073/pnas.2015224118 |
0.674 |
|
| 2020 |
Liang W, Cai X, Dai M. Cu-catalyzed hydroxycyclopropanol ring-opening cyclization to tetrahydrofurans and tetrahydropyrans: short total syntheses of hyperiones. Chemical Science. 12: 1311-1316. PMID 34163894 DOI: 10.1039/d0sc05556e |
0.303 |
|
| 2020 |
Kyei-Baffour K, Davis DC, Boskovic Z, Kato N, Dai M. Natural product-inspired aryl isonitriles as a new class of antimalarial compounds against drug-resistant parasites. Bioorganic & Medicinal Chemistry. 28: 115678. PMID 32912433 DOI: 10.1016/J.Bmc.2020.115678 |
0.692 |
|
| 2020 |
Cai X, Liang W, Liu M, Li X, Dai M. Catalytic Hydroxycyclopropanol Ring-Opening Carbonylative Lactonization to Fused Bicyclic Lactones. Journal of the American Chemical Society. PMID 32687339 DOI: 10.1021/Jacs.0C06179 |
0.43 |
|
| 2020 |
Peery RC, Kyei-Baffour K, Dong Z, de Andrade Horn P, Dai M, Liu JY, Zhang JT. Synthesis and identification of a novel lead targeting survivin dimerization for proteasome-dependent degradation. Journal of Medicinal Chemistry. PMID 32421328 DOI: 10.1021/Acs.Jmedchem.0C00475 |
0.344 |
|
| 2020 |
Jiang B, Dai M. Synthetic Studies toward the Hamigerans with a 6-7-5 Tricyclic Core. Organic Letters. PMID 32401527 DOI: 10.1021/Acs.Orglett.0C01253 |
0.393 |
|
| 2020 |
Huang L, Li X, Zhang W, Ung N, Liu N, Yin X, Li Y, Mcewan RE, Dilkes BP, Dai M, Hicks GR, Raikhel NV, Staiger CJ, Zhang C. Endosidin20 Targets the Cellulose Synthase Catalytic Domain to Inhibit Cellulose Biosynthesis. The Plant Cell. PMID 32327535 DOI: 10.1105/Tpc.20.00202 |
0.325 |
|
| 2019 |
Kyei-Baffour K, Mohammad H, Seleem MN, Dai M. Second-generation aryl isonitrile compounds targeting multidrug-resistant Staphylococcus aureus. Bioorganic & Medicinal Chemistry. PMID 30926310 DOI: 10.1016/J.Bmc.2019.03.034 |
0.327 |
|
| 2019 |
Luo Y, Yin X, Dai M. Total Synthesis of trans-Resorcylide via Macrocyclic Stille Carbonylation. The Journal of Antibiotics. PMID 30760840 DOI: 10.1038/S41429-019-0145-4 |
0.452 |
|
| 2019 |
Cai X, Liang W, Dai M. Total syntheses via cyclopropanols Tetrahedron. 75: 193-208. DOI: 10.1016/J.Tet.2018.11.026 |
0.408 |
|
| 2018 |
Davis DC, Hoch DG, Wu L, Abegg D, Martin BS, Zhang ZY, Adibekian A, Dai M. Total Synthesis, Biological Evaluation, and Target Identification of Rare Abies Sesquiterpenoids. Journal of the American Chemical Society. PMID 30461272 DOI: 10.1021/Jacs.8B07652 |
0.391 |
|
| 2018 |
Dai M, Ma K, Yin X. Total Syntheses of Bisdehydroneostemoninine and Bisdehydro-stemoninine by Catalytic Carbonylative Spirolactonization. Angewandte Chemie (International Ed. in English). PMID 30230670 DOI: 10.1002/Anie.201809114 |
0.415 |
|
| 2018 |
Ma K, Martin BS, Yin X, Dai M. Natural product syntheses via carbonylative cyclizations. Natural Product Reports. PMID 29923586 DOI: 10.1039/C8Np00033F |
0.425 |
|
| 2018 |
Ye Z, Adhikari S, Xia Y, Dai M. Expedient syntheses of N-heterocycles via intermolecular amphoteric diamination of allenes. Nature Communications. 9: 721. PMID 29459667 DOI: 10.1038/S41467-018-03085-3 |
0.387 |
|
| 2018 |
Cai X, Bai Y, Dai M. Total Syntheses of Spinosyn A Synlett. 29: 2623-2632. DOI: 10.1055/S-0037-1610249 |
0.394 |
|
| 2018 |
Ye Z, Cai X, Li J, Dai M. Catalytic Cyclopropanol Ring Opening for Divergent Syntheses of γ-Butyrolactones and δ-Ketoesters Containing All-Carbon Quaternary Centers Acs Catalysis. 8: 5907-5914. DOI: 10.1021/Acscatal.8B00711 |
0.387 |
|
| 2017 |
Li Y, Wei M, Dai M. Gold Catalysis-Facilitated Rapid Synthesis of the Daphnane/Tigliane Tricyclic Core. Tetrahedron. 73: 4172-4177. PMID 28890579 DOI: 10.1016/J.Tet.2016.11.005 |
0.413 |
|
| 2017 |
Li Y, Yin X, Dai M. Catalytic macrolactonizations for natural product synthesis. Natural Product Reports. PMID 28853755 DOI: 10.1039/C7Np00038C |
0.414 |
|
| 2017 |
Li Y, Dai M. Total Syntheses of the Reported Structures of Curcusone I and J via Tandem Gold Catalysis. Angewandte Chemie (International Ed. in English). PMID 28708291 DOI: 10.1002/Anie.201706845 |
0.407 |
|
| 2017 |
Yin X, Mohammad H, Eldesouky HE, Abdelkhalek A, Seleem MN, Dai M. Rapid synthesis of bicyclic lactones via palladium-catalyzed aminocarbonylative lactonizations. Chemical Communications (Cambridge, England). PMID 28492641 DOI: 10.1039/C7Cc02494K |
0.389 |
|
| 2017 |
Mohammad H, Kyei-Baffour K, Younis W, Davis DC, Eldesouky H, Seleem MN, Dai M. Investigation of aryl isonitrile compounds with potent, broad-spectrum antifungal activity. Bioorganic & Medicinal Chemistry. PMID 28385596 DOI: 10.1016/J.Bmc.2017.03.035 |
0.314 |
|
| 2017 |
Bai Y, Davis DC, Dai M. Natural Product Synthesis via Palladium-Catalyzed Carbonylation. The Journal of Organic Chemistry. PMID 28170262 DOI: 10.1021/Acs.Joc.7B00009 |
0.396 |
|
| 2017 |
Davis DC, Haskins CW, Dai M. Radical Cyclopropanol Ring Opening Initiated Tandem Cyclizations for Efficient Synthesis of Phenanthridines and Oxindoles Synlett. 28: 913-918. DOI: 10.1055/S-0036-1590427 |
0.397 |
|
| 2017 |
Gettys KE, Ye Z, Dai M. Recent Advances in Piperazine Synthesis Synthesis. 49: 2589-2604. DOI: 10.1055/S-0036-1589491 |
0.385 |
|
| 2016 |
Bai Y, Shen X, Li Y, Dai M. Total Synthesis of (-)-Spinosyn A via Carbonylative Macrolactonization. Journal of the American Chemical Society. PMID 27510806 DOI: 10.1021/Jacs.6B07585 |
0.452 |
|
| 2016 |
Davis DC, Walker KL, Hu C, Zare RN, Waymouth RM, Dai M. Catalytic Carbonylative Spirolactonization of Hydroxycyclopropanols. Journal of the American Chemical Society. PMID 27459274 DOI: 10.1021/Jacs.6B06573 |
0.388 |
|
| 2016 |
Ye Z, Gettys KE, Dai M. Opportunities and challenges for direct C-H functionalization of piperazines. Beilstein Journal of Organic Chemistry. 12: 702-15. PMID 27340462 DOI: 10.3762/Bjoc.12.70 |
0.326 |
|
| 2016 |
Lin Z, Tan L, Yang Y, Dai M, Tureček F, Ouyang Z, Xia Y. Gas-phase reactions of cyclopropenylidene with protonated alkyl amines. The Analyst. PMID 26978226 DOI: 10.1039/C6An00235H |
0.351 |
|
| 2016 |
Sun W, Shi L, Ye Z, Mu Y, Liu C, Zhao J, Chen L, Li Q, Yang T, Yan L, Wan Q, Wu S, Liu Y, Wang G, Luo Z, ... ... Dai M, et al. Association between the change in body mass index from early adulthood to midlife and subsequent type 2 diabetes mellitus. Obesity (Silver Spring, Md.). PMID 26833544 DOI: 10.1002/oby.21336 |
0.319 |
|
| 2015 |
Bai Y, Dai M. Strategies and Methods for the Synthesis of Anticancer Natural Product Neopeltolide and its Analogs. Current Organic Chemistry. 19: 871-885. PMID 27182194 DOI: 10.2174/1385272819666150119225149 |
0.396 |
|
| 2015 |
Ye Z, Gettys KE, Shen X, Dai M. Copper-Catalyzed Cyclopropanol Ring Opening Csp(3)-Csp(3) Cross-Couplings with (Fluoro)Alkyl Halides. Organic Letters. PMID 26635251 DOI: 10.1021/Acs.Orglett.5B03096 |
0.395 |
|
| 2015 |
Huang YH, Lee YC, Li Q, Chen CJ, Hsu WL, Lou PJ, Zhu C, Pan J, Shen H, Ma H, Cai L, He B, Wang Y, Zhou X, Ji Q, ... ... Dai M, et al. Family History of Cancer and Head and Neck Cancer Risk in a Chinese Population. Asian Pacific Journal of Cancer Prevention : Apjcp. 16: 8003-8. PMID 26625833 DOI: 10.7314/Apjcp.2015.16.17.8003 |
0.346 |
|
| 2015 |
Li S, Lee YA, Li Q, Chen CJ, Hsu WL, Lou PJ, Zhu C, Pan J, Shen H, Ma H, Cai L, He B, Wang Y, Zhou X, Ji Q, ... ... Dai M, et al. Oral lesions, chronic diseases and the risk of head and neck cancer. Oral Oncology. PMID 26526128 DOI: 10.1016/J.Oraloncology.2015.10.014 |
0.333 |
|
| 2015 |
Davis DC, Mohammad H, Kyei-Baffour K, Younis W, Creemer CN, Seleem MN, Dai M. Discovery and characterization of aryl isonitriles as a new class of compounds versus methicillin- and vancomycin-resistant Staphylococcus aureus. European Journal of Medicinal Chemistry. 101: 384-90. PMID 26164843 DOI: 10.1016/J.Ejmech.2015.06.031 |
0.315 |
|
| 2015 |
Chou DH, Vetere A, Choudhary A, Scully SS, Schenone M, Tang A, Gomez R, Burns SM, Lundh M, Vital T, Comer E, Faloon PW, Dan?ík V, Ciarlo C, Paulk J, ... Dai M, et al. Kinase-Independent Small-Molecule Inhibition of JAK-STAT Signaling. Journal of the American Chemical Society. 137: 7929-34. PMID 26042473 DOI: 10.1021/Jacs.5B04284 |
0.722 |
|
| 2015 |
Ye Z, Dai M. An Umpolung Strategy for the Synthesis of β-Aminoketones via Copper-Catalyzed Electrophilic Amination of Cyclopropanols. Organic Letters. 17: 2190-3. PMID 25885943 DOI: 10.1021/Acs.Orglett.5B00828 |
0.38 |
|
| 2015 |
Li Y, Ye Z, Bellman TM, Chi T, Dai M. Efficient Synthesis of β-CF3/SCF3-Substituted Carbonyls via Copper-Catalyzed Electrophilic Ring-Opening Cross-Coupling of Cyclopropanols. Organic Letters. 17: 2186-9. PMID 25885795 DOI: 10.1021/Acs.Orglett.5B00782 |
0.386 |
|
| 2015 |
Ye Z, Brust TF, Watts VJ, Dai M. Palladium-catalyzed regio- and stereoselective γ-arylation of tertiary allylic amines: identification of potent adenylyl cyclase inhibitors. Organic Letters. 17: 892-5. PMID 25668690 DOI: 10.1021/Ol503748T |
0.405 |
|
| 2015 |
Lee HJ, Zhang W, Zhang D, Yang Y, Liu B, Barker EL, Buhman KK, Slipchenko LV, Dai M, Cheng JX. Assessing cholesterol storage in live cells and C. elegans by stimulated Raman scattering imaging of phenyl-Diyne cholesterol. Scientific Reports. 5: 7930. PMID 25608867 DOI: 10.1038/Srep07930 |
0.306 |
|
| 2014 |
Yang Y, Dai M. Total Syntheses of Lyconadins: Finding Efficiency and Diversity. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 25: 2093-2098. PMID 25866447 DOI: 10.1055/S-0034-1378319 |
0.414 |
|
| 2014 |
Liu Y, Asnani A, Zou L, Bentley VL, Yu M, Wang Y, Dellaire G, Sarkar KS, Dai M, Chen HH, Sosnovik DE, Shin JT, Haber DA, Berman JN, Chao W, et al. Visnagin protects against doxorubicin-induced cardiomyopathy through modulation of mitochondrial malate dehydrogenase. Science Translational Medicine. 6: 266ra170. PMID 25504881 DOI: 10.1126/Scitranslmed.3010189 |
0.465 |
|
| 2014 |
Yang Y, Bai Y, Sun S, Dai M. Biosynthetically inspired divergent approach to monoterpene indole alkaloids: total synthesis of mersicarpine, leuconodines B and D, leuconoxine, melodinine E, leuconolam, and rhazinilam. Organic Letters. 16: 6216-9. PMID 25412144 DOI: 10.1021/Ol503150C |
0.431 |
|
| 2014 |
Zhang W, Haskins CW, Yang Y, Dai M. Synthesis of nitriles via palladium-catalyzed water shuffling from amides to acetonitrile. Organic & Biomolecular Chemistry. 12: 9109-12. PMID 25316145 DOI: 10.1039/C4Ob01825G |
0.443 |
|
| 2014 |
Bai Y, Davis DC, Dai M. Synthesis of tetrahydropyran/tetrahydrofuran-containing macrolides by palladium-catalyzed alkoxycarbonylative macrolactonizations. Angewandte Chemie (International Ed. in English). 53: 6519-22. PMID 24825410 DOI: 10.1002/Anie.201403006 |
0.404 |
|
| 2014 |
Yang Y, Haskins CW, Zhang W, Low PL, Dai M. Divergent total syntheses of lyconadins A and C. Angewandte Chemie (International Ed. in English). 53: 3922-5. PMID 24596132 DOI: 10.1002/Anie.201400416 |
0.433 |
|
| 2013 |
Boskovic ZV, Hussain MM, Adams DJ, Dai M, Schreiber SL. Synthesis of piperlogs and analysis of their effects on cells. Tetrahedron. 69. PMID 24273350 DOI: 10.1016/J.Tet.2013.05.080 |
0.732 |
|
| 2013 |
Hartwell KA, Miller PG, Mukherjee S, Kahn AR, Stewart AL, Logan DJ, Negri JM, Duvet M, Järås M, Puram R, Dancik V, Al-Shahrour F, Kindler T, Tothova Z, Chattopadhyay S, ... ... Dai M, et al. Niche-based screening identifies small-molecule inhibitors of leukemia stem cells. Nature Chemical Biology. 9: 840-8. PMID 24161946 DOI: 10.1038/Nchembio.1367 |
0.746 |
|
| 2012 |
Peng F, Dai M, Angeles AR, Danishefsky SJ. Permuting Diels-Alder and Robinson Annulation Stereopatterns. Chemical Science (Royal Society of Chemistry : 2010). 3: 3076-3080. PMID 23139855 DOI: 10.1039/C2Sc20868G |
0.762 |
|
| 2012 |
Adams DJ, Dai M, Pellegrino G, Wagner BK, Stern AM, Shamji AF, Schreiber SL. Synthesis, cellular evaluation, and mechanism of action of piperlongumine analogs. Proceedings of the National Academy of Sciences of the United States of America. 109: 15115-20. PMID 22949699 DOI: 10.1073/Pnas.1212802109 |
0.751 |
|
| 2011 |
Wang Z, Dai M, Park PK, Danishefsky SJ. Synthetic studies toward (+)-cortistatin A. Tetrahedron. 67: 10249-10260. PMID 22879684 DOI: 10.1016/J.Tet.2011.10.026 |
0.649 |
|
| 2011 |
Luo T, Dai M, Zheng SL, Schreiber SL. Syntheses of α-pyrones using gold-catalyzed coupling reactions. Organic Letters. 13: 2834-6. PMID 21534543 DOI: 10.1021/Ol200794W |
0.661 |
|
| 2009 |
Hayden AE, DeChancie J, George AH, Dai M, Yu M, Danishefsky SJ, Houk KN. Origins of the regioselectivities in the Diels-Alder reactions of vinylindenes with 1,4-quinone monoketal and acrolein dienophiles. The Journal of Organic Chemistry. 74: 6770-6. PMID 19663431 DOI: 10.1021/Jo901473H |
0.512 |
|
| 2009 |
Dai M, Danishefsky SJ. An oxidative dearomatization cyclization model for cortistatin A Heterocycles. 77: 157-161. DOI: 10.3987/Com-08-S(F)6 |
0.455 |
|
| 2008 |
Dai M, Wang Z, Danishefsky SJ. A novel α,β-unsaturated nitrone-aryne [3+2] cycloaddition and its application in the synthesis of the cortistatin core. Tetrahedron Letters. 49: 6613-6616. PMID 19924220 DOI: 10.1016/J.Tetlet.2008.09.019 |
0.625 |
|
| 2008 |
Dai M, Danishefsky SJ. A concise synthesis of the cortistatin core. Tetrahedron Letters. 49: 6610-6612. PMID 19924219 DOI: 10.1016/J.Tetlet.2008.09.018 |
0.516 |
|
| 2008 |
Lei X, Dai M, Hua Z, Danishefsky SJ. Biomimetic total synthesis of tricycloillicinone and mechanistic studies toward the rearrangement of prenyl phenyl ethers. Tetrahedron Letters. 49: 6383-6385. PMID 19890380 DOI: 10.1016/J.Tetlet.2008.07.184 |
0.544 |
|
| 2008 |
Dai M, Krauss IJ, Danishefsky SJ. Total synthesis of spirotenuipesines A and B. The Journal of Organic Chemistry. 73: 9576-83. PMID 18973385 DOI: 10.1021/Jo8016814 |
0.741 |
|
| 2008 |
Li Z, Gao Y, Tang Y, Dai M, Wang G, Wang Z, Yang Z. Total synthesis of crisamicin A. Organic Letters. 10: 3017-20. PMID 18553973 DOI: 10.1021/Ol800977N |
0.44 |
|
| 2007 |
Dai M, Danishefsky SJ. The total synthesis of spirotenuipesines A and B. Journal of the American Chemical Society. 129: 3498-9. PMID 17335213 DOI: 10.1021/ja069164r |
0.387 |
|
| 2007 |
Liu Y, Lu K, Dai M, Wang K, Wu W, Chen J, Quan J, Yang Z. An efficient one-pot asymmetric synthesis of biaryl compounds via Diels-Alder/retro-Diels-Alder cascade reactions. Organic Letters. 9: 805-8. PMID 17266319 DOI: 10.1021/Ol063013B |
0.508 |
|
| 2007 |
Dai M, Sarlah D, Yu M, Danishefsky SJ, Jones GO, Houk KN. Highly selective Diels-Alder reactions of directly connected enyne dienophiles. Journal of the American Chemical Society. 129: 645-57. PMID 17227028 DOI: 10.1021/Ja065762U |
0.519 |
|
| 2005 |
Tang Y, Zhang Y, Dai M, Luo T, Deng L, Chen J, Yang Z. A highly efficient synthesis of the FGH ring of micrandilactone A. Application of thioureas as ligands in the Co-catalyzed Pauson-Khand reaction and Pd-catalyzed carbonylative annulation. Organic Letters. 7: 885-8. PMID 15727466 DOI: 10.1021/Ol047394+ |
0.721 |
|
| 2005 |
Liang B, Dai M, Chen J, Yang Z. Copper-free sonogashira coupling reaction with PdCl2 in water under aerobic conditions. The Journal of Organic Chemistry. 70: 391-3. PMID 15624959 DOI: 10.1021/Jo048599Z |
0.414 |
|
| 2004 |
Xiong Z, Wang N, Dai M, Li A, Chen J, Yang Z. Synthesis of novel palladacycles and their application in Heck and Suzuki reactions under aerobic conditions. Organic Letters. 6: 3337-40. PMID 15355046 DOI: 10.1021/Ol048749S |
0.455 |
|
| 2004 |
Dai M, Liang B, Wang C, Chen J, Yang Z. Synthesis of a novel C2-symmetric thiourea and its application in the Pd-catalyzed cross-coupling reactions with arenediazonium salts under aerobic conditions. Organic Letters. 6: 221-4. PMID 14723533 DOI: 10.1021/Ol036182U |
0.475 |
|
| 2003 |
Dai M, Wang C, Dong G, Xiang J, Luo T, Liang B, Chen J, Yang Z. Development of Thiourea-Based Ligands for the Palladium-Catalyzed Bis(methoxycarbonylation) of Terminal Olefins European Journal of Organic Chemistry. 2003: 4346-4348. DOI: 10.1002/Ejoc.200300543 |
0.609 |
|
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