Year |
Citation |
Score |
2024 |
Ling T, Arroyo-Cruz LV, Smither WR, Seighman EK, Martínez-Montemayor MM, Rivas F. Early Preclinical Studies of Ergosterol Peroxide and Biological Evaluation of Its Derivatives. Acs Omega. 9: 37117-37127. PMID 39246459 DOI: 10.1021/acsomega.4c04350 |
0.671 |
|
2024 |
Arroyo-Cruz LV, Sagardía-González S, Miller K, Ling T, Rivas F, Martínez-Montemayor MM. Selective Antineoplastic Potential of Fractionated Caribbean Native Species Extracts on Triple-Negative Breast Cancer Cells. Pharmaceuticals (Basel, Switzerland). 17. PMID 39065715 DOI: 10.3390/ph17070864 |
0.628 |
|
2024 |
Barras BJ, Ling T, Rivas F. Recent Advances in Chemistry and Antioxidant/Anticancer Biology of Monoterpene and Meroterpenoid Natural Product. Molecules (Basel, Switzerland). 29. PMID 38202861 DOI: 10.3390/molecules29010279 |
0.677 |
|
2022 |
Ling T, Boyd L, Rivas F. Triterpenoids as Reactive Oxygen Species Modulators of Cell Fate. Chemical Research in Toxicology. 35: 569-584. PMID 35312315 DOI: 10.1021/acs.chemrestox.1c00428 |
0.63 |
|
2020 |
Ling T, Hadi V, Bollinger J, Rivas F. Identification of rapid access to polycyclic systems via a base-catalyzed cascade cyclization reaction and their biological evaluation. Bioorganic Chemistry. 99: 103846. PMID 32334195 DOI: 10.1016/J.Bioorg.2020.103846 |
0.679 |
|
2019 |
Ling T, Miller DJ, Lang W, Griffith E, Rodríguez-Cortés A, El Ayachi I, Palacios G, Min J, Miranda-Carboni GA, Lee RE, Rivas F. Mechanistic insight on the mode of action of colletoic acid. Journal of Medicinal Chemistry. PMID 31294974 DOI: 10.1021/Acs.Jmedchem.9B00187 |
0.648 |
|
2019 |
Ling T, Lang WH, Maier J, Quintana Centurion M, Rivas F. Cytostatic and Cytotoxic Natural Products against Cancer Cell Models. Molecules (Basel, Switzerland). 24. PMID 31130671 DOI: 10.3390/Molecules24102012 |
0.688 |
|
2019 |
Ling T, Lang WH, Craig J, Potts MB, Budhraja A, Opferman J, Bollinger J, Maier J, Marsico TD, Rivas F. Studies of Jatrogossone A as a Reactive Oxygen Species Inducer in Cancer Cellular Models. Journal of Natural Products. PMID 31084028 DOI: 10.1021/Acs.Jnatprod.8B01087 |
0.682 |
|
2019 |
Ling T, Lang WH, Martinez-Montemayor MM, Rivas F. Development of ergosterol peroxide probes for cellular localisation studies. Organic & Biomolecular Chemistry. PMID 31025693 DOI: 10.1039/C9Ob00145J |
0.672 |
|
2019 |
Martínez-Montemayor MM, Ling T, Suárez-Arroyo IJ, Ortiz-Soto G, Santiago-Negrón CL, Lacourt-Ventura MY, Valentín-Acevedo A, Lang WH, Rivas F. Identification of Biologically Active Compounds and Synthesis of Improved Derivatives That Confer Anti-cancer Activities . Frontiers in Pharmacology. 10: 115. PMID 30837881 DOI: 10.3389/Fphar.2019.00115 |
0.672 |
|
2019 |
Santiago CL, Rivas F, Ling T, Suarez-Arroyo IJ, Ortiz G, Lacourt MY, Valentin A, Lang WH, Martínez-Montemayor MM. Abstract 1869: Mechanistic evaluation of ergosterol peroxide onin vitrobreast cancer models Cancer Research. DOI: 10.1158/1538-7445.Sabcs18-1869 |
0.638 |
|
2018 |
Ling T, Maier J, Das S, Budhraja A, Bassett R, Potts MB, Shelat A, Rankovic Z, Opferman JT, Rivas F. Identification of substituted 5-membered heterocyclic compounds as potential anti-leukemic agents. European Journal of Medicinal Chemistry. 164: 391-398. PMID 30611980 DOI: 10.1016/J.Ejmech.2018.12.059 |
0.679 |
|
2018 |
Ling T, Lang W, Feng X, Das S, Maier J, Jeffries C, Shelat A, Rivas F. Novel vitexin-inspired scaffold against leukemia. European Journal of Medicinal Chemistry. 146: 501-510. PMID 29407975 DOI: 10.1016/J.Ejmech.2018.01.004 |
0.68 |
|
2016 |
Gautam LN, Ling T, Lang W, Rivas F. Anti-proliferative evaluation of monoterpene derivatives against leukemia. European Journal of Medicinal Chemistry. 113: 75-80. PMID 26922230 DOI: 10.1016/J.Ejmech.2016.02.034 |
0.646 |
|
2016 |
Ling T, Gautam LN, Griffith E, Das S, Lang W, Shadrick WR, Shelat A, Lee R, Rivas F. Synthesis and evaluation of colletoic acid core derivatives. European Journal of Medicinal Chemistry. 110: 126-132. PMID 26820555 DOI: 10.1016/J.Ejmech.2016.01.027 |
0.649 |
|
2016 |
Rivas F, Ling T. Advances toward the Synthesis of Functionalized γ-Lactams Organic Preparations and Procedures International. 48: 254-295. DOI: 10.1080/00304948.2016.1165059 |
0.65 |
|
2016 |
Ling T, Rivas F. All-carbon quaternary centers in natural products and medicinal chemistry: recent advances Tetrahedron. 72: 6729-6777. DOI: 10.1016/J.Tet.2016.09.002 |
0.625 |
|
2015 |
Ling T, Tran M, González MA, Gautam LN, Connelly M, Wood RK, Fatima I, Miranda-Carboni G, Rivas F. (+)-Dehydroabietylamine derivatives target triple-negative breast cancer. European Journal of Medicinal Chemistry. 102: 9-13. PMID 26241873 DOI: 10.1016/J.Ejmech.2015.07.034 |
0.651 |
|
2013 |
Zhai B, Clark J, Ling T, Connelly M, Medina-Bolivar F, Rivas F. Antimalarial evaluation of the chemical constituents of hairy root culture of Bixa orellana L. Molecules (Basel, Switzerland). 19: 756-66. PMID 24406786 DOI: 10.3390/Molecules19010756 |
0.657 |
|
2013 |
Ling T, Griffith E, Mitachi K, Rivas F. Scalable and divergent total synthesis of (+)-colletoic acid, a selective 11β-hydroxysteroid dehydrogenase type 1 inhibitor. Organic Letters. 15: 5790-3. PMID 24175735 DOI: 10.1021/Ol402842U |
0.685 |
|
2013 |
Hadi V, Hotard M, Ling T, Salinas YG, Palacios G, Connelly M, Rivas F. Evaluation of Jatropha isabelli natural products and their synthetic analogs as potential antimalarial therapeutic agents. European Journal of Medicinal Chemistry. 65: 376-80. PMID 23747806 DOI: 10.1016/J.Ejmech.2013.04.030 |
0.68 |
|
2012 |
Mitachi K, Salinas YG, Connelly M, Jensen N, Ling T, Rivas F. Synthesis and structure-activity relationship of disubstituted benzamides as a novel class of antimalarial agents. Bioorganic & Medicinal Chemistry Letters. 22: 4536-9. PMID 22727641 DOI: 10.1016/J.Bmcl.2012.05.124 |
0.675 |
|
2011 |
Ling T, Xu J, Smith R, Ali A, Cantrell CL, Theodorakis EA. Synthesis of (-)-callicarpenal, a potent arthropod-repellent. Tetrahedron. 67: 3023-3029. PMID 21643472 DOI: 10.1016/J.Tet.2011.02.078 |
0.641 |
|
2006 |
Nicolaou KC, Koftis TV, Vyskocil S, Petrovic G, Tang W, Frederick MO, Chen DY, Li Y, Ling T, Yamada YM. Total synthesis and structural elucidation of azaspiracid-1. Final assignment and total synthesis of the correct structure of azaspiracid-1. Journal of the American Chemical Society. 128: 2859-72. PMID 16506764 DOI: 10.1021/Ja054750Q |
0.542 |
|
2006 |
Nicolaou KC, Chen DY, Li Y, Uesaka N, Petrovic G, Koftis TV, Bernal F, Frederick MO, Govindasamy M, Ling T, Pihko PM, Tang W, Vyskocil S. Total synthesis and structural elucidation of azaspiracid-1. Synthesis-based analysis of originally proposed structures and indication of their non-identity to the natural product. Journal of the American Chemical Society. 128: 2258-67. PMID 16478179 DOI: 10.1021/Ja054748Z |
0.511 |
|
2006 |
Nicolaou K, Koftis T, Vyskocil S, Petrovic G, Tang W, Frederick M, Chen D, Ling T, Li Y, Yamada Y. Synthesis and Structural Elucidation of Azaspiracid-1 Synfacts. 2006: 0748-0748. DOI: 10.1055/S-2006-941937 |
0.408 |
|
2006 |
Ito E, Frederick MO, Koftis TV, Tang W, Petrovic G, Ling T, Nicolaou KC. Structure toxicity relationships of synthetic azaspiracid-1 and analogs in mice Harmful Algae. 5: 586-591. DOI: 10.1016/J.Hal.2005.11.005 |
0.407 |
|
2004 |
Nicolaou KC, Chen DY, Huang X, Ling T, Bella M, Snyder SA. Chemistry and biology of diazonamide A: first total synthesis and confirmation of the true structure. Journal of the American Chemical Society. 126: 12888-96. PMID 15469286 DOI: 10.1021/Ja040092I |
0.456 |
|
2004 |
Nicolaou KC, Koftis TV, Vyskocil S, Petrovic G, Ling T, Yamada YM, Tang W, Frederick MO. Structural revision and total synthesis of azaspiracid-1, part 2: definition of the ABCD domain and total synthesis. Angewandte Chemie (International Ed. in English). 43: 4318-24. PMID 15368381 DOI: 10.1002/Anie.200460696 |
0.386 |
|
2004 |
Nicolaou KC, Vyskocil S, Koftis TV, Yamada YM, Ling T, Chen DY, Tang W, Petrovic G, Frederick MO, Li Y, Satake M. Structural revision and total synthesis of azaspiracid-1, part 1: intelligence gathering and tentative proposal. Angewandte Chemie (International Ed. in English). 43: 4312-8. PMID 15368380 DOI: 10.1002/Anie.200460695 |
0.466 |
|
2004 |
Nicolaou KC, Chen DY, Huang X, Ling T, Bella M, Snyder SA. Chemistry and Biology of Diazonamide A: First Total Synthesis and Confirmation of the True Structure [J. Am. Chem. Soc.2004,126, 12888−12896]. Journal of the American Chemical Society. 126: 15316-15316. DOI: 10.1021/Ja040823E |
0.458 |
|
2004 |
Theodorakis EA, Ling T, Rueden EJ, Poupon E, Kim SH. Chapter 4 Quinone sesquiterpenes: A challenge for the development of a new synthetic methodology Strategies and Tactics in Organic Synthesis. 5: 111-131. DOI: 10.1016/S1874-6004(04)80027-3 |
0.656 |
|
2004 |
Nicolaou KC, Vyskocil S, Koftis TV, Yamada YMA, Ling T, Chen DY, Tang W, Petrovic G, Frederick MO, Li Y, Satake M. Cover Picture: Structural Revision and Total Synthesis of Azaspiracid-1, Part 1: Intelligence Gathering and Tentative Proposal (Angew. Chem. Int. Ed. 33/2004) Angewandte Chemie International Edition. 43: 4239-4239. DOI: 10.1002/Anie.200490111 |
0.46 |
|
2004 |
Nicolaou KC, Vyskocil S, Koftis TV, Yamada YMA, Ling T, Chen DY, Tang W, Petrovic G, Frederick MO, Li Y, Satake M. Titelbild: Structural Revision and Total Synthesis of Azaspiracid-1, Part 1: Intelligence Gathering and Tentative Proposal (Angew. Chem. 33/2004) Angewandte Chemie. 116: 4335-4335. DOI: 10.1002/Ange.200490110 |
0.467 |
|
2003 |
Lam T, Ling T, Chowdhury C, Chao TH, Bahjat FR, Lloyd GK, Moldawer LL, Palladino MA, Theodorakis EA. Synthesis of a novel family of diterpenes and their evaluation as anti-inflammatory agents. Bioorganic & Medicinal Chemistry Letters. 13: 3217-21. PMID 12951096 DOI: 10.1016/S0960-894X(03)00669-3 |
0.77 |
|
2003 |
Nicolaou KC, Chen DY, Li Y, Qian W, Ling T, Vyskocil S, Koftis TV, Govindasamy M, Uesaka N. Total synthesis of the proposed azaspiracid-1 structure, part 2: coupling of the C1-C20, C21-C27, and C28-C40 fragments and completion of the synthesis. Angewandte Chemie (International Ed. in English). 42: 3649-53. PMID 12916037 DOI: 10.1002/Anie.200351826 |
0.405 |
|
2003 |
Nicolaou KC, Li Y, Uesaka N, Koftis TV, Vyskocil S, Ling T, Govindasamy M, Qian W, Bernal F, Chen DY. Total synthesis of the proposed azaspiracid-1 structure, part 1: construction of the enantiomerically pure C1-C20, C21-C27, and C28-C40 fragments. Angewandte Chemie (International Ed. in English). 42: 3643-8. PMID 12916036 DOI: 10.1002/Anie.200351825 |
0.477 |
|
2002 |
Ling T, Poupon E, Rueden EJ, Kim SH, Theodorakis EA. Unified synthesis of quinone sesquiterpenes based on a radical decarboxylation and quinone addition reaction. Journal of the American Chemical Society. 124: 12261-7. PMID 12371868 DOI: 10.1021/Ja027517Q |
0.636 |
|
2002 |
Nicolaou KC, Bella M, Chen DY, Huang X, Ling T, Snyder SA. Total synthesis of diazonamide A. Angewandte Chemie (International Ed. in English). 41: 3495-9. PMID 12298077 DOI: 10.1002/1521-3773(20020916)41:18<3495::Aid-Anie3495>3.0.Co;2-7 |
0.491 |
|
2002 |
Ling T, Poupon E, Rueden EJ, Theodorakis EA. Synthesis of (-)-ilimaquinone via a radical decarboxylation and quinone addition reaction. Organic Letters. 4: 819-22. PMID 11869136 DOI: 10.1021/Ol025501Z |
0.601 |
|
2002 |
Ling T, Rivas F, Theodorakis EA. Stereoselective synthesis of the fully functionalized core fragment of terpentecin Tetrahedron Letters. 43: 9019-9022. DOI: 10.1016/S0040-4039(02)02314-6 |
0.74 |
|
2001 |
Ling T, Chowdhury C, Kramer BA, Vong BG, Palladino MA, Theodorakis EA. Enantioselective synthesis of the antiinflammatory agent (-)-acanthoic acid. The Journal of Organic Chemistry. 66: 8843-53. PMID 11749614 DOI: 10.1021/Jo0159035 |
0.768 |
|
2001 |
Haidekker MA, Ling T, Anglo M, Stevens HY, Frangos JA, Theodorakis EA. New fluorescent probes for the measurement of cell membrane viscosity. Chemistry & Biology. 8: 123-31. PMID 11251287 DOI: 10.1016/S1074-5521(00)90061-9 |
0.515 |
|
2000 |
Ling T, Kramer BA, Palladino MA, Theodorakis EA. Stereoselective synthesis of (-)-acanthoic acid. Organic Letters. 2: 2073-6. PMID 10891233 DOI: 10.1021/Ol0060578 |
0.638 |
|
2000 |
Drouet KE, Ling T, Tran HV, Theodorakis EA. Enantioselective synthesis of the [6,6] spiroketal core of reveromycin A. Organic Letters. 2: 207-10. PMID 10814283 DOI: 10.1021/Ol991290V |
0.628 |
|
1999 |
Ling T, Xiang AX, Theodorakis EA. Enantioselective Total Synthesis of Avarol and Avarone. Angewandte Chemie (International Ed. in English). 38: 3089-3091. PMID 10540432 DOI: 10.1002/(Sici)1521-3773(19991018)38:20<3089::Aid-Anie3089>3.0.Co;2-W |
0.775 |
|
1999 |
Ling T, Xiang AX, Theodorakis EA. Enantioselektive Totalsynthese von Avarol und Avaron Angewandte Chemie. 111: 3277-3279. DOI: 10.1002/(Sici)1521-3757(19991018)111:20<3277::Aid-Ange3277>3.0.Co;2-M |
0.714 |
|
1998 |
Xiang AX, Watson DA, Ling T, Theodorakis EA. Total Synthesis of Clerocidin via a Novel, Enantioselective Homoallenylboration Methodology. The Journal of Organic Chemistry. 63: 6774-6775. PMID 11672290 DOI: 10.1021/Jo981331L |
0.788 |
|
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