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• Ravi Sankar Archan, Arunachalam Sermarajan, Gnanasekaran Ramachandran: A computational study to determine the role of σ-hole in Br/OH substituted nido-carborane and its binding capabilities. Journal of Molecular Graphics and Modelling 2024, 127, 108680. <https://doi.org/10.1016/j.jmgm.2023.108680>
• He Qindi, Zhao Xiaofei, Wu Donglin, Jia Siming, Liu Canlin, Cheng Zitian, Huang Fei, Chen Yadong, Lu Tao, Lu Shuai: Hydrophobic tag-based protein degradation: Development, opportunity and challenge. European Journal of Medicinal Chemistry 2023, 260, 115741. <https://doi.org/10.1016/j.ejmech.2023.115741>
• Avdeeva Varvara V., Privalov Viktor I., Kubasov Alexey S., Nikiforova Svetlana E., Malinina Elena A., Kuznetsov Nikolay T.: 2D COSY 11B NMR spectroscopy in the interpretation of the structures of iso and trans isomers of the macropolyhedral boron cluster [B20H18]2–. Inorganica Chimica Acta 2023, 555, 121564. <https://doi.org/10.1016/j.ica.2023.121564>
• Marco José F., Dávalos-Prado Juan Z., Hnyk Drahomír, Holub Josef, Oña Ofelia B., Alcoba Diego R., Ferrer Maxime, Elguero José, Lain Luis, Torre Alicia, Oliva-Enrich Josep M.: Two Shared Icosahedral Metallacarboranes through Iron: A Joint Experimental and Theoretical Refinement of Mössbauer Spectrum in [Fe(1,2-C2B9H11)2]Cs. ACS Omega 2023, 8, 13993. <https://doi.org/10.1021/acsomega.3c00422>
• Zhang Cai-Yan, Cao Ke, Liu Dechun, Yang Han-Bo, Teng Chao-Chao, Li Bo, Yang Junxiao: Iridium-catalyzed selective amination of B(4)–H for the synthesis of o-carborane-fused indolines. Dalton Trans. 2023, 52, 2933. <https://doi.org/10.1039/D3DT00316G>
• Ha Tae-Jin, Im Dong-Kyung, Kim Seung-Min, Lee Jong-Dae: 1,2-Diphenyl-o-carborane and Its Chromium Derivatives: Synthesis, Characterization, X-ray Structural Studies, and Biological Evaluations. Molecules 2023, 28, 4942. <https://doi.org/10.3390/molecules28134942>
• Avdeeva V.V., Malinina E.A., Kuznetsov N.T.: Boron cluster anions and their derivatives in complexation reactions. Coordination Chemistry Reviews 2022, 469, 214636. <https://doi.org/10.1016/j.ccr.2022.214636>
• Shishkanova Tatiana V., Sinica Alla: Electrochemically deposited cobalt bis(dicarbollide) derivative and the detection of neuroblastoma markers on the electrode surface. Journal of Electroanalytical Chemistry 2022, 921, 116674. <https://doi.org/10.1016/j.jelechem.2022.116674>
• Avdeeva Varvara V., Kubasov Aleksey S., Korolenko Svetlana E., Privalov Viktor I., Malinina Elena A., Kuznetsov Nikolay T.: Iron(II), cobalt(II), and nickel(II) complexes with 1,10-phenanthroline and 2,2′-bipyridyl and the macropolyhedral borane cluster [trans-B20H18]2- as counterion. Polyhedron 2022, 217, 115740. <https://doi.org/10.1016/j.poly.2022.115740>
• Nikiforova Svetlana E., Kubasov Alexey S., Goeva Lyudmila V., Avdeeva Varvara V., Malinina Elena A., Kuznetsov Nikolay T.: Features of the formation of d10 metal complexes with benzimidazoles derivatives in the presence of the closo-decaborate anion. Polyhedron 2022, 226, 116108. <https://doi.org/10.1016/j.poly.2022.116108>
• Matveev Evgenii Yu., Avdeeva Varvara V., Zhizhin Konstantin Yu., Malinina Elena A., Kuznetsov Nikolay T.: Effect of Nature of Substituents on Coordination Properties of Mono- and Disubstituted Derivatives of Boron Cluster Anions [BnHn]2– (n = 10, 12) and Carboranes with exo-Polyhedral B–X Bonds (X = N, O, S, Hal). Inorganics 2022, 10, 238. <https://doi.org/10.3390/inorganics10120238>
• Vaňková Eva, Lokočová Kristýna, Kašparová Petra, Hadravová Romana, Křížová Ivana, Maťátková Olga, Masák Jan, Šícha Václav: Cobalt Bis-Dicarbollide Enhances Antibiotics Action towards Staphylococcus epidermidis Planktonic Growth Due to Cell Envelopes Disruption. Pharmaceuticals 2022, 15, 534. <https://doi.org/10.3390/ph15050534>
• Kugler Michael, Nekvinda Jan, Holub Josef, El Anwar Suzan, Das Viswanath, Šícha Václav, Pospíšilová Klára, Fábry Milan, Král Vlastimil, Brynda Jiří, Kašička Václav, Hajdúch Marián, Řezáčová Pavlína, Grüner Bohumír: Inhibitors of CA IX Enzyme Based on Polyhedral Boron Compounds. ChemBioChem 2021, 22, 2741. <https://doi.org/10.1002/cbic.202100121>
• Gruzdev Dmitry A., Levit Galina L., Krasnov Victor P., Charushin Valery N.: Carborane-containing amino acids and peptides: Synthesis, properties and applications. Coordination Chemistry Reviews 2021, 433, 213753. <https://doi.org/10.1016/j.ccr.2020.213753>
• Murphy Neville, McCarthy Elan, Dwyer Róisín, Farràs Pau: Boron clusters as breast cancer therapeutics. Journal of Inorganic Biochemistry 2021, 218, 111412. <https://doi.org/10.1016/j.jinorgbio.2021.111412>
• Druzina Anna A., Shmalko Akim V., Sivaev Igor B., Bregadze Vladimir I.: Cyclic oxonium derivatives of cobalt and iron bis(dicarbollides) and their use in organic synthesis. Russ. Chem. Rev. 2021, 90, 785. <https://doi.org/10.1070/RCR5000>
• Ferrer-Ugalde Albert, González-Campo Arántzazu, Planas José Giner, Viñas Clara, Teixidor Francesc, Sáez Isabel M., Núñez Rosario: Tuning the Liquid Crystallinity of Cholesteryl-o-Carborane Dyads: Synthesis, Structure, Photoluminescence, and Mesomorphic Properties. Crystals 2021, 11, 133. <https://doi.org/10.3390/cryst11020133>
• Druzina Anna A., Zhidkova Olga B., Dudarova Nadezhda V., Nekrasova Natalia A., Suponitsky Kyrill Yu., Timofeev Sergey V., Bregadze Vladimir I.: Synthesis of Zwitter-Ionic Conjugate of Nido-Carborane with Cholesterol. Molecules 2021, 26, 6687. <https://doi.org/10.3390/molecules26216687>
• Tse Edwin G., Houston Sevan D., Williams Craig M., Savage G. Paul, Rendina Louis M., Hallyburton Irene, Anderson Mark, Sharma Raman, Walker Gregory S., Obach R. Scott, Todd Matthew H.: Nonclassical Phenyl Bioisosteres as Effective Replacements in a Series of Novel Open-Source Antimalarials. J. Med. Chem. 2020, 63, 11585. <https://doi.org/10.1021/acs.jmedchem.0c00746>
• Kellert Martin, Hoppenz Paul, Lönnecke Peter, Worm Dennis J., Riedl Bernd, Koebberling Johannes, Beck-Sickinger Annette G., Hey-Hawkins Evamarie: Tuning a modular system – synthesis and characterisation of a boron-rich s-triazine-based carboxylic acid and amine bearing a galactopyranosyl moiety. Dalton Trans. 2020, 49, 57. <https://doi.org/10.1039/C9DT04031E>
• Teixeira Ricardo G., Marques Fernanda, Robalo M. Paula, Fontrodona Xavier, Garcia M. Helena, Geninatti Crich Simonetta, Viñas Clara, Valente Andreia: Ruthenium carboranyl complexes with 2,2′-bipyridine derivatives for potential bimodal therapy application. RSC Adv. 2020, 10, 16266. <https://doi.org/10.1039/D0RA01522A>
• Kugler Michael, Holub Josef, Brynda Jiří, Pospíšilová Klára, Anwar Suzan El, Bavol Dmytro, Havránek Miroslav, Král Vlastimil, Fábry Milan, Grüner Bohumír, Řezáčová Pavlína: The structural basis for the selectivity of sulfonamido dicarbaboranes toward cancer-associated carbonic anhydrase IX. Journal of Enzyme Inhibition and Medicinal Chemistry 2020, 35, 1800. <https://doi.org/10.1080/14756366.2020.1816996>
• Kellert Martin, Sárosi Imola, Rajaratnam Rajathees, Meggers Eric, Lönnecke Peter, Hey-Hawkins Evamarie: Ruthenacarborane–Phenanthroline Derivatives as Potential Metallodrugs. Molecules 2020, 25, 2322. <https://doi.org/10.3390/molecules25102322>
• Jena Bibhuti Bhusan, Satish Lakkoji, Mahanta Chandra Sekhara, Swain Biswa Ranjan, Sahoo Harekrushna, Dash Barada P., Satapathy Rashmirekha: Interaction of carborane-appended trimer with bovine serum albumin: A spectroscopic investigation. Inorganica Chimica Acta 2019, 491, 52. <https://doi.org/10.1016/j.ica.2019.03.035>
• Nekvinda Jan, Grüner Bohumír, Gabel Detlef, Nau Werner M., Assaf Khaleel I.: Host–Guest Chemistry of Carboranes: Synthesis of Carboxylate Derivatives and Their Binding to Cyclodextrins. Chemistry A European J 2018, 24, 12970. <https://doi.org/10.1002/chem.201802134>
• Fernandez-Alvarez Roberto, Ďorďovič Vladimír, Uchman Mariusz, Matějíček Pavel: Amphiphiles without Head-and-Tail Design: Nanostructures Based on the Self-Assembly of Anionic Boron Cluster Compounds. Langmuir 2018, 34, 3541. <https://doi.org/10.1021/acs.langmuir.7b03306>
• Kuhnert Robert, Sárosi Menyhárt‐Botond, George Sven, Lönnecke Peter, Hofmann Bettina, Steinhilber Dieter, Murganic Blagoje, Mijatovic Sanja, Maksimovic‐Ivanic Danijela, Hey‐Hawkins Evamarie: CarbORev‐5901: The First Carborane‐Based Inhibitor of the 5‐Lipoxygenase Pathway. ChemMedChem 2017, 12, 1081. <https://doi.org/10.1002/cmdc.201700309>
• Shen Yunjun, Liu Jiyong, Sattasatchuchana Tosaporn, Baldridge Kim K., Duttwyler Simon: Transition Metal Complexes of a Monocarba‐closo‐dodecaborate Ligand via B–H Activation. Eur J Inorg Chem 2017, 2017, 4420. <https://doi.org/10.1002/ejic.201700677>
• Anufriev Sergey A., Sivaev Igor B., Suponitsky Kyrill Yu., Godovikov Ivan A., Bregadze Vladimir I.: Synthesis of 10‐Methylsulfide and 10‐Alkylmethylsulfonium nido‐Carborane Derivatives: B–H···π Interactions between the B–H–B Hydrogen Atom and Alkyne Group in 10‐RC≡CCH2S(Me)‐7,8‐C2B9H11. Eur J Inorg Chem 2017, 2017, 4436. <https://doi.org/10.1002/ejic.201700785>
• Kvasničková Eva, Masák Jan, Čejka Jan, Maťátková Olga, Šícha Václav: Preparation, characterization, and the selective antimicrobial activity of N-alkylammonium 8-diethyleneglycol cobalt bis-dicarbollide derivatives. Journal of Organometallic Chemistry 2017, 827, 23. <https://doi.org/10.1016/j.jorganchem.2016.10.037>
• He Tianyu, Misuraca Jennifer C., Musah Rabi A.: “Carboranyl-cysteine”—Synthesis, Structure and Self-Assembly Behavior of a Novel α-Amino Acid. Sci Rep 2017, 7. <https://doi.org/10.1038/s41598-017-16926-w>
• Shen Yunjun, Pan Yani, Liu Jiyong, Sattasathuchana Tosaporn, Baldridge Kim K., Duttwyler Simon: Synthesis and full characterization of an iridium B–H activation intermediate of the monocarba-closo-dodecaborate anion. Chem. Commun. 2017, 53, 176. <https://doi.org/10.1039/C6CC08121E>
• Shen Yunjun, Pan Yani, Zhang Kang, Liang Xuewei, Liu Jiyong, Spingler Bernhard, Duttwyler Simon: B–H functionalization of the monocarba-closo-dodecaborate anion by rhodium and iridium catalysis. Dalton Trans. 2017, 46, 3135. <https://doi.org/10.1039/C7DT00269F>
• Saha Bapan, Bhattacharyya Pradip Kr.: B–Hb⋯π interaction in borane–graphene complexes: coronene as a case study. New J. Chem. 2017, 41, 5040. <https://doi.org/10.1039/C7NJ00057J>
• Żołnierczyk Jolanta D., Olejniczak Agnieszka B., Mieczkowski Adam, Błoński Jerzy Z., Kiliańska Zofia M., Robak Tadeusz, Leśnikowski Zbigniew J.: In vitro antileukemic activity of novel adenosine derivatives bearing boron cluster modification. Bioorganic & Medicinal Chemistry 2016, 24, 5076. <https://doi.org/10.1016/j.bmc.2016.08.028>
• Adamska Anna, Rumijowska-Galewicz Anna, Ruszczynska Anna, Studzińska Mirosława, Jabłońska Agnieszka, Paradowska Edyta, Bulska Ewa, Munier-Lehmann Hélene, Dziadek Jarosław, Leśnikowski Zbigniew J., Olejniczak Agnieszka B.: Anti-mycobacterial activity of thymine derivatives bearing boron clusters. European Journal of Medicinal Chemistry 2016, 121, 71. <https://doi.org/10.1016/j.ejmech.2016.05.030>
• Zelinskii Genrikh E., Belov Alexander S., Vologzhanina Anna V., Pavlov Alexander A., Novikov Valentin V., Varzatskii Oleg A., Voloshin Yan Z.: Synthesis, structure and ADMET properties of the monoribbed-functionalized iron(II) clathrochelates with terminal DNA-relevant groups. Inorganica Chimica Acta 2016, 448, 7. <https://doi.org/10.1016/j.ica.2016.04.006>
• Leśnikowski Zbigniew J.: Challenges and Opportunities for the Application of Boron Clusters in Drug Design. J. Med. Chem. 2016, 59, 7738. <https://doi.org/10.1021/acs.jmedchem.5b01932>
• Ďorďovič Vladimír, Tošner Zdeněk, Uchman Mariusz, Zhigunov Alexander, Reza Mehedi, Ruokolainen Janne, Pramanik Goutam, Cígler Petr, Kalíková Květa, Gradzielski Michael, Matějíček Pavel: Stealth Amphiphiles: Self-Assembly of Polyhedral Boron Clusters. Langmuir 2016, 32, 6713. <https://doi.org/10.1021/acs.langmuir.6b01995>
• Ďorďovič Vladimír, Uchman Mariusz, Reza Mehedi, Ruokolainen Janne, Zhigunov Alexander, Ivankov Olexandr I., Matějíček Pavel: Cation-sensitive compartmentalization in metallacarborane containing polymer nanoparticles. RSC Adv. 2016, 6, 9884. <https://doi.org/10.1039/C5RA27588A>
• Leśnikowski Zbigniew J.: Recent developments with boron as a platform for novel drug design. Expert Opinion on Drug Discovery 2016, 11, 569. <https://doi.org/10.1080/17460441.2016.1174687>
• Uchman Mariusz, Ďorďovič Vladimír, Tošner Zdeněk, Matějíček Pavel: Classical Amphiphilic Behavior of Nonclassical Amphiphiles: A Comparison of Metallacarborane Self‐Assembly with SDS Micellization. Angewandte Chemie 2015, 127, 14319. <https://doi.org/10.1002/ange.201506545>
• Uchman Mariusz, Ďorďovič Vladimír, Tošner Zdeněk, Matějíček Pavel: Classical Amphiphilic Behavior of Nonclassical Amphiphiles: A Comparison of Metallacarborane Self‐Assembly with SDS Micellization. Angew Chem Int Ed 2015, 54, 14113. <https://doi.org/10.1002/anie.201506545>
• Goszczyński Tomasz M., Kowalski Konrad, Leśnikowski Zbigniew J., Boratyński Janusz: Solid state, thermal synthesis of site-specific protein–boron cluster conjugates and their physicochemical and biochemical properties. Biochimica et Biophysica Acta (BBA) - General Subjects 2015, 1850, 411. <https://doi.org/10.1016/j.bbagen.2014.11.015>
• Romero-Canelón Isolda, Phoenix Ben, Pitto-Barry Anaïs, Tran Johanna, Soldevila-Barreda Joan J., Kirby Nigel, Green Stuart, Sadler Peter J., Barry Nicolas P.E.: Arene ruthenium dithiolato–carborane complexes for boron neutron capture therapy (BNCT). Journal of Organometallic Chemistry 2015, 796, 17. <https://doi.org/10.1016/j.jorganchem.2015.05.011>
• Satapathy Rashmirekha, Dash Barada P., Mahanta Chandra Sekhara, Swain Biswa Ranjan, Jena Bibhuti Bhusan, Hosmane Narayan S.: Glycoconjugates of polyhedral boron clusters. Journal of Organometallic Chemistry 2015, 798, 13. <https://doi.org/10.1016/j.jorganchem.2015.06.027>
• Galliamova Lidiia A., Varaksin Mikhail V., Chupakhin Oleg N., Slepukhin Pavel A., Charushin Valery N.: Heterocyclic and Open-Chain Carboranes via Transition-Metal-Free C–H Functionalization of Mono- and Diazine-N-oxides. Organometallics 2015, 34, 5285. <https://doi.org/10.1021/acs.organomet.5b00736>
• Lo Rabindranath, Fanfrlík Jindřich, Lepšík Martin, Hobza Pavel: The properties of substituted 3D-aromatic neutral carboranes: the potential for σ-hole bonding. Phys. Chem. Chem. Phys. 2015, 17, 20814. <https://doi.org/10.1039/C5CP03617H>
• Voloshin Yan Z., Novikov Valentin V., Nelyubina Yulia V.: Recent advances in biological applications of cage metal complexes. RSC Adv. 2015, 5, 72621. <https://doi.org/10.1039/C5RA10949C>
• Frank René, Ahrens Verena, Boehnke Solveig, Hofmann Sven, Kellert Martin, Saretz Stefan, Pandey Souvik, Sárosi Menyhárt, Bartók Ágota, Beck-Sickinger Annette G., Hey-Hawkins Evamarie: Carbaboranes – more than just phenyl mimetics. Pure and Applied Chemistry 2015, 87, 163. <https://doi.org/10.1515/pac-2014-1006>
• Sýkora David, Řídká Kristýna, Tesařová Eva, Kalíková Květa, Kaplánek Robert, Král Vladimír: Characterization of novel metallacarborane-based sorbents by linear solvation energy relationships. Journal of Chromatography A 2014, 1371, 220. <https://doi.org/10.1016/j.chroma.2014.10.081>
• Wilkinson Shane M., Gunosewoyo Hendra, Barron Melissa L., Boucher Aurelie, McDonnell Michelle, Turner Peter, Morrison Daniel E., Bennett Maxwell R., McGregor Iain S., Rendina Louis M., Kassiou Michael: The First CNS-Active Carborane: A Novel P2X7 Receptor Antagonist with Antidepressant Activity. ACS Chem. Neurosci. 2014, 5, 335. <https://doi.org/10.1021/cn500054n>
• Barry Nicolas P. E., Kemp Thomas F., Sadler Peter J., Hanna John V.: A multinuclear 1H, 13C and 11B solid-state MAS NMR study of 16- and 18-electron organometallic ruthenium and osmium carborane complexes. Dalton Trans. 2014, 43, 4945. <https://doi.org/10.1039/C3DT53589D>
• Barry Nicolas P. E., Pitto-Barry Anaïs, Romero-Canelón Isolda, Tran Johanna, Soldevila-Barreda Joan J., Hands-Portman Ian, Smith Corinne J., Kirby Nigel, Dove Andrew P., O'Reilly Rachel K., Sadler Peter J.: Precious metal carborane polymer nanoparticles: characterisation of micellar formulations and anticancer activity. Faraday Discuss. 2014, 175, 229. <https://doi.org/10.1039/C4FD00098F>
• Mader Pavel, Pecina Adam, Cígler Petr, Lepšík Martin, Šícha Václav, Hobza Pavel, Grüner Bohumír, Fanfrlík Jindřich, Brynda Jiří, Řezáčová Pavlína: Carborane-Based Carbonic Anhydrase Inhibitors: Insight into CAII/CAIX Specificity from a High-Resolution Crystal Structure, Modeling, and Quantum Chemical Calculations. BioMed Research International 2014, 2014, 1. <https://doi.org/10.1155/2014/389869>
• Brynda Jiří, Mader Pavel, Šícha Václav, Fábry Milan, Poncová Kristýna, Bakardiev Mario, Grüner Bohumír, Cígler Petr, Řezáčová Pavlína: Carborane‐Based Carbonic Anhydrase Inhibitors. Angewandte Chemie 2013, 125, 14005. <https://doi.org/10.1002/ange.201307583>
• Brynda Jiří, Mader Pavel, Šícha Václav, Fábry Milan, Poncová Kristýna, Bakardiev Mario, Grüner Bohumír, Cígler Petr, Řezáčová Pavlína: Carborane‐Based Carbonic Anhydrase Inhibitors. Angew Chem Int Ed 2013, 52, 13760. <https://doi.org/10.1002/anie.201307583>
• Matějíček Pavel, Uchman Mariusz, Lepšík Martin, Srnec Martin, Zedník Jiří, Kozlík Petr, Kalíková Květa: Preparation and Separation of Telechelic Carborane‐Containing Poly(ethylene glycol)s. ChemPlusChem 2013, 78, 528. <https://doi.org/10.1002/cplu.201300046>
• Olejniczak Agnieszka B., Kierzek Ryszard, Wickstrom Eric, Lesnikowski Zbigniew J.: Synthesis, physicochemical and biochemical studies of anti-IRS-1 oligonucleotides containing carborane and/or metallacarborane modification. Journal of Organometallic Chemistry 2013, 747, 201. <https://doi.org/10.1016/j.jorganchem.2013.05.022>
• Pecina Adam, Lepšík Martin, Řezáč Jan, Brynda Jiří, Mader Pavel, Řezáčová Pavlína, Hobza Pavel, Fanfrlík Jindřich: QM/MM Calculations Reveal the Different Nature of the Interaction of Two Carborane-Based Sulfamide Inhibitors of Human Carbonic Anhydrase II. J. Phys. Chem. B 2013, 117, 16096. <https://doi.org/10.1021/jp410216m>
• Ďorďovič Vladimír, Uchman Mariusz, Procházka Karel, Zhigunov Alexander, Pleštil Josef, Nykänen Antti, Ruokolainen Janne, Matějíček Pavel: Hybrid Nanospheres Formed by Intermixed Double-Hydrophilic Block Copolymer Poly(ethylene oxide)-block-poly(2-ethyloxazoline) with High Content of Metallacarboranes. Macromolecules 2013, 46, 6881. <https://doi.org/10.1021/ma4013626>
• Rak Jakub, Dejlová Barbora, Lampová Hana, Kaplánek Robert, Matějíček Pavel, Cígler Petr, Král Vladimír: On the Solubility and Lipophilicity of Metallacarborane Pharmacophores. Mol. Pharmaceutics 2013, 10, 1751. <https://doi.org/10.1021/mp300565z>
• Wojtczak Blazej A., Olejniczak Agnieszka B., Wang Liya, Eriksson Staffan, Lesnikowski Zbigniew J.: Phosphorylation of Nucleoside-Metallacarborane and Carborane Conjugates by Nucleoside Kinases. Nucleosides, Nucleotides and Nucleic Acids 2013, 32, 571. <https://doi.org/10.1080/15257770.2013.838259>
• Bednarska Katarzyna, Olejniczak Agnieszka B., Piskala Agnieszka, Klink Magdalena, Sulowska Zofia, Lesnikowski Zbigniew J.: Effect of adenosine modified with a boron cluster pharmacophore on reactive oxygen species production by human neutrophils. Bioorganic & Medicinal Chemistry 2012, 20, 6621. <https://doi.org/10.1016/j.bmc.2012.09.039>
• Wu Chunhui, Shi Lixin, Li Qingning, Jiang Hui, Selke Matthias, Yan Hong, Wang Xuemei: New strategy of efficient inhibition of cancer cells by carborane carboxylic acid–CdTe nanocomposites. Nanomedicine: Nanotechnology, Biology and Medicine 2012, 8, 860. <https://doi.org/10.1016/j.nano.2011.10.011>
• Rak Jakub, Jakubek Milan, Kaplánek Robert, Král Vladimír: Low-Melting Salts Based on a Glycolated Cobalt Bis(dicarbollide) Anion. Inorg. Chem. 2012, 51, 4099. <https://doi.org/10.1021/ic2023665>
• Kaplánek Robert, Martásek Pavel, Grüner Bohumír, Panda Satya, Rak Jakub, Masters Bettie Sue Siler, Král Vladimír, Roman Linda J.: Nitric Oxide Synthases Activation and Inhibition by Metallacarborane-Cluster-Based Isoform-Specific Affectors. J. Med. Chem. 2012, 55, 9541. <https://doi.org/10.1021/jm300805x>
• Farràs Pau, Juárez-Pérez Emilio J., Lepšík Martin, Luque Rafael, Núñez Rosario, Teixidor Francesc: Metallacarboranes and their interactions: theoretical insights and their applicability. Chemical Society Review 2012, 41, 3445. <https://doi.org/10.1039/c2cs15338f>
• Stadlbauer Sven, Frank René, Scholz Matthias, Boehnke Solveig, Ahrens Verena M., Beck-Sickinger Annette G., Hey-Hawkins Evamarie: Imitation and modification of bioactive lead structures via integration of boron clusters. Pure and Applied Chemistry 2012, 84, 2289. <https://doi.org/10.1351/PAC-CON-11-11-02>
• Ciani Laura, Ristori Sandra: Boron as a platform for new drug design. Expert Opinion on Drug Discovery 2012, 7, 1017. <https://doi.org/10.1517/17460441.2012.717530>
• Meggers Eric: Von konventionellen zu ungewöhnlichen Gerüsten für Enzyminhibitoren: das Streben nach Spezifität. Angewandte Chemie 2011, 123, 2490. <https://doi.org/10.1002/ange.201005673>
• Meggers Eric: From Conventional to Unusual Enzyme Inhibitor Scaffolds: The Quest for Target Specificity. Angew Chem Int Ed 2011, 50, 2442. <https://doi.org/10.1002/anie.201005673>
• Pathak Biswarup, Samanta  Devleena, Ahuja Rajeev, Jena Purusottam: Borane Derivatives: A New Class of Super‐ and Hyperhalogens. ChemPhysChem 2011, 12, 2423. <https://doi.org/10.1002/cphc.201100320>
• Ohta Kiminori, Goto Tokuhito, Fujii Shinya, Kawahata Masatoshi, Oda Akifumi, Ohta Shigeru, Yamaguchi Kentaro, Hirono Shuichi, Endo Yasuyuki: Crystal structure, docking study and structure–activity relationship of carborane-containing androgen receptor antagonist 3-(12-hydroxymethyl-1,12-dicarba-closo-dodecaboran-1-yl)benzonitrile. Bioorganic & Medicinal Chemistry 2011, 19, 3540. <https://doi.org/10.1016/j.bmc.2011.04.017>
• Wu Chunhui, Ye Hongde, Bai Wenjuan, Li Qingning, Guo Dadong, Lv Gang, Yan Hong, Wang Xuemei: New Potential Anticancer Agent of Carborane Derivatives: Selective Cellular Interaction and Activity of Ferrocene-Substituted Dithio-o-carborane Conjugates. Bioconjugate Chem. 2011, 22, 16. <https://doi.org/10.1021/bc100158b>
• Calvaresi Matteo, Zerbetto Francesco: In Silico Carborane Docking to Proteins and Potential Drug Targets. J. Chem. Inf. Model. 2011, 51, 1882. <https://doi.org/10.1021/ci200216z>
• Scholz Matthias, Hey-Hawkins Evamarie: Carbaboranes as Pharmacophores: Properties, Synthesis, and Application Strategies. Chem. Rev. 2011, 111, 7035. <https://doi.org/10.1021/cr200038x>
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