6.
Jones G, Willett P, Glen R, Leach A, Taylor R
. Development and validation of a genetic algorithm for flexible docking. J Mol Biol. 1997; 267(3):727-48.
DOI: 10.1006/jmbi.1996.0897.
View
7.
Giske C, Turnidge J, Canton R, Kahlmeter G
. Update from the European Committee on Antimicrobial Susceptibility Testing (EUCAST). J Clin Microbiol. 2021; 60(3):e0027621.
PMC: 8925892.
DOI: 10.1128/JCM.00276-21.
View
8.
Laxmi S, Rajitha G, Rajitha B, Rao A
. Photochemical synthesis and anticancer activity of barbituric acid, thiobarbituric acid, thiosemicarbazide, and isoniazid linked to 2-phenyl indole derivatives. J Chem Biol. 2016; 9(2):57-63.
PMC: 4830754.
DOI: 10.1007/s12154-015-0148-y.
View
9.
Li M, Chen C, Ling C, Zhou J, Ji B, Wu Y
. Cytotoxicity and structure-activity relationships of four alpha-N-heterocyclic thiosemicarbazone derivatives crystal structure of 2-acetylpyrazine thiosemicarbazone. Bioorg Med Chem Lett. 2009; 19(10):2704-6.
DOI: 10.1016/j.bmcl.2009.03.135.
View
10.
Groom C, Bruno I, Lightfoot M, Ward S
. The Cambridge Structural Database. Acta Crystallogr B Struct Sci Cryst Eng Mater. 2016; 72(Pt 2):171-9.
PMC: 4822653.
DOI: 10.1107/S2052520616003954.
View
11.
Ayoup M, Wahby Y, Abdel-Hamid H, Abu-Serie M, Ramadan S, Barakat A
. Reinvestigation of Passerini and Ugi scaffolds as multistep apoptotic inducers dual modulation of caspase 3/7 and P53-MDM2 signaling for halting breast cancer. RSC Adv. 2023; 13(40):27722-27737.
PMC: 10509784.
DOI: 10.1039/d3ra04029a.
View
12.
Umamatheswari S, Balaji B, Ramanathan M, Kabilan S
. Synthesis, stereochemistry, antimicrobial evaluation and QSAR studies of 2,6-diaryltetrahydropyran-4-one thiosemicarbazones. Eur J Med Chem. 2011; 46(4):1415-24.
DOI: 10.1016/j.ejmech.2011.01.029.
View
13.
Thanh Nguyen D, Le T, Trang Bui T
. Antioxidant activities of thiosemicarbazones from substituted benzaldehydes and N-(tetra-O-acetyl-β-D-galactopyranosyl)thiosemicarbazide. Eur J Med Chem. 2013; 60:199-207.
DOI: 10.1016/j.ejmech.2012.10.004.
View
14.
Pitucha M, Korga-Plewko A, Czylkowska A, Rogalewicz B, Drozd M, Iwan M
. Influence of Complexation of Thiosemicarbazone Derivatives with Cu (II) Ions on Their Antitumor Activity against Melanoma Cells. Int J Mol Sci. 2021; 22(6).
PMC: 8002893.
DOI: 10.3390/ijms22063104.
View
15.
dilovic I, Rubcic M, Vrdoljak V, Kraljevic Pavelic S, Kralj M, Piantanida I
. Novel thiosemicarbazone derivatives as potential antitumor agents: Synthesis, physicochemical and structural properties, DNA interactions and antiproliferative activity. Bioorg Med Chem. 2008; 16(9):5189-98.
DOI: 10.1016/j.bmc.2008.03.006.
View
16.
Sever B, Altintop M, Ciftci G, Ozdemir A
. A New Series of Triazolothiadiazines as Potential Anticancer Agents for Targeted Therapy of Non-Small Cell Lung and Colorectal Cancers: Design, Synthesis, In silico and In vitro Studies Providing Mechanistic Insight into Their Anticancer Potencies. Med Chem. 2020; 17(10):1104-1128.
DOI: 10.2174/1573406416666201021142832.
View
17.
Chen R, Huo L, Jaiswal Y, Huang J, Zhong Z, Zhong J
. Design, Synthesis, Antimicrobial, and Anticancer Activities of Acridine Thiosemicarbazides Derivatives. Molecules. 2019; 24(11).
PMC: 6600397.
DOI: 10.3390/molecules24112065.
View
18.
Verdonk M, Cole J, Hartshorn M, Murray C, Taylor R
. Improved protein-ligand docking using GOLD. Proteins. 2003; 52(4):609-23.
DOI: 10.1002/prot.10465.
View
19.
Vandresen F, Falzirolli H, Almeida Batista S, da Silva-Giardini A, de Oliveira D, Catharino R
. Novel R-(+)-limonene-based thiosemicarbazones and their antitumor activity against human tumor cell lines. Eur J Med Chem. 2014; 79:110-6.
DOI: 10.1016/j.ejmech.2014.03.086.
View
20.
Nitiss J
. Targeting DNA topoisomerase II in cancer chemotherapy. Nat Rev Cancer. 2009; 9(5):338-50.
PMC: 2748742.
DOI: 10.1038/nrc2607.
View