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For: He H, Wang X, Shi L, Yin W, Yang Z, He H, Liang Y. Synthesis, antitumor activity and mechanism of action of novel 1,3-thiazole derivatives containing hydrazide–hydrazone and carboxamide moiety. Bioorganic & Medicinal Chemistry Letters 2016;26:3263-70. [DOI: 10.1016/j.bmcl.2016.05.059] [Cited by in Crossref: 43] [Cited by in F6Publishing: 36] [Article Influence: 7.2] [Reference Citation Analysis]
Number Citing Articles
1 Bakale RP, Naik GN, Machakanur SS, Mangannavar CV, Muchchandi IS, Gudasi KB. Structural characterization and antimicrobial activities of transition metal complexes of a hydrazone ligand. Journal of Molecular Structure 2018;1154:92-9. [DOI: 10.1016/j.molstruc.2017.10.035] [Cited by in Crossref: 10] [Cited by in F6Publishing: 3] [Article Influence: 2.5] [Reference Citation Analysis]
2 Kauthale S, Tekale S, Damale M, Sangshetti J, Pawar R. Synthesis, antioxidant, antifungal, molecular docking and ADMET studies of some thiazolyl hydrazones. Bioorganic & Medicinal Chemistry Letters 2017;27:3891-6. [DOI: 10.1016/j.bmcl.2017.06.043] [Cited by in Crossref: 25] [Cited by in F6Publishing: 16] [Article Influence: 5.0] [Reference Citation Analysis]
3 Cheng Y, Avula SR, Gao WW, Addla D, Tangadanchu VKR, Zhang L, Lin JM, Zhou CH. Multi-targeting exploration of new 2-aminothiazolyl quinolones: Synthesis, antimicrobial evaluation, interaction with DNA, combination with topoisomerase IV and penetrability into cells. Eur J Med Chem 2016;124:935-45. [PMID: 27769037 DOI: 10.1016/j.ejmech.2016.10.011] [Cited by in Crossref: 47] [Cited by in F6Publishing: 45] [Article Influence: 7.8] [Reference Citation Analysis]
4 Zhang Z, Shu B, Zhang Y, Deora GS, Li Q. 2,4,5-Trisubstituted Thiazole: A Privileged Scaffold in Drug Design and Activity Improvement. CTMC 2020;20:2535-77. [DOI: 10.2174/1568026620999200917153856] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
5 Kavitha K, Srikrishna D, Dubey PK, Aparna P. An efficient one-pot four-component Gewald reaction: Synthesis of substituted 2-aminothiophenes with coumarin–thiazole scaffolds under environmentally benign conditions. Journal of Sulfur Chemistry 2019;40:195-208. [DOI: 10.1080/17415993.2018.1556275] [Cited by in Crossref: 8] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
6 Almatary AM, Elmorsy MA, El Husseiny WM, Selim KB, El-Sayed MA. Design, synthesis, and molecular modeling of heterocyclic bioisostere as potent PDE4 inhibitors. Arch Pharm (Weinheim) 2018;351:e1700403. [PMID: 29573453 DOI: 10.1002/ardp.201700403] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
7 Popiołek Ł, Gawrońska-Grzywacz M, Berecka-Rycerz A, Paruch K, Piątkowska-Chmiel I, Natorska-Chomicka D, Herbet M, Gumieniczek A, Dudka J, Wujec M. New benzenesulphonohydrazide derivatives as potential antitumour agents. Oncol Lett 2020;20:136. [PMID: 32934704 DOI: 10.3892/ol.2020.12047] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
8 Cuartas V, Robledo SM, Vélez ID, Crespo MDP, Sortino M, Zacchino S, Nogueras M, Cobo J, Upegui Y, Pineda T, Yepes L, Insuasty B. New thiazolyl‐pyrazoline derivatives bearing nitrogen mustard as potential antimicrobial and antiprotozoal agents. Arch Pharm 2020;353. [DOI: 10.1002/ardp.201900351] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 2.5] [Reference Citation Analysis]
9 Maklad RM, AbdelHafez EMN, Abdelhamid D, Aly OM. Tubulin inhibitors: Discovery of a new scaffold targeting extra-binding residues within the colchicine site through anchoring substituents properly adapted to their pocket by a semi-flexible linker. Bioorg Chem 2020;99:103767. [PMID: 32325332 DOI: 10.1016/j.bioorg.2020.103767] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
10 Khalil TE, Soliman SM, Khalil NA, El‐faham A, Foro S, El‐dissouky A. Synthesis, structure, X‐ray photoelectron spectroscopy (XPS), and antimicrobial, anticancer, and antioxidant activities of Co (III) complexes based on the antihypertensive hydralazine. Applied Organom Chemis. [DOI: 10.1002/aoc.6565] [Reference Citation Analysis]
11 de Santana TI, Barbosa MO, Gomes PATM, da Cruz ACN, da Silva TG, Leite ACL. Synthesis, anticancer activity and mechanism of action of new thiazole derivatives. Eur J Med Chem 2018;144:874-86. [PMID: 29329071 DOI: 10.1016/j.ejmech.2017.12.040] [Cited by in Crossref: 74] [Cited by in F6Publishing: 47] [Article Influence: 14.8] [Reference Citation Analysis]
12 Li Z, Yang D, Geng P, Zhang J, Wei H, Hu B, Guo Q, Zhang X, Guo W, Zhao B, Yu B, Ma L, Liu H. Design, synthesis and biological evaluation of [1,2,3]triazolo[4,5- d ]pyrimidine derivatives possessing a hydrazone moiety as antiproliferative agents. European Journal of Medicinal Chemistry 2016;124:967-80. [DOI: 10.1016/j.ejmech.2016.10.022] [Cited by in Crossref: 44] [Cited by in F6Publishing: 39] [Article Influence: 7.3] [Reference Citation Analysis]
13 Chen X, Wang X, Song J, Yang Q, Huang C, Liu W. Efficient construction of C–N and C–S bonds in 2-iminothiazoles via cascade reaction of enaminones with potassium thiocyanate. Org Biomol Chem 2017;15:3611-5. [DOI: 10.1039/c7ob00306d] [Cited by in Crossref: 25] [Cited by in F6Publishing: 2] [Article Influence: 5.0] [Reference Citation Analysis]
14 Chen P, Song X, Fan Y, Kong W, Zhang H, Sun R. Investigation of Novel Pesticides with Insecticidal and Antifungal Activities: Design, Synthesis and SAR Studies of Benzoylpyrimidinylurea Derivatives. Molecules 2018;23:E2203. [PMID: 30200298 DOI: 10.3390/molecules23092203] [Cited by in Crossref: 2] [Article Influence: 0.5] [Reference Citation Analysis]
15 Vaškevičienė I, Paketurytė V, Zubrienė A, Kantminienė K, Mickevičius V, Matulis D. N-Sulfamoylphenyl- and N-sulfamoylphenyl-N-thiazolyl-β-alanines and their derivatives as inhibitors of human carbonic anhydrases. Bioorg Chem 2017;75:16-29. [PMID: 28888097 DOI: 10.1016/j.bioorg.2017.08.017] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
16 Krátký M, Konečná K, Brablíková M, Janoušek J, Pflégr V, Maixnerová J, Trejtnar F, Vinšová J. Iodinated 1,2-diacylhydrazines, benzohydrazide-hydrazones and their analogues as dual antimicrobial and cytotoxic agents. Bioorg Med Chem 2021;41:116209. [PMID: 34015704 DOI: 10.1016/j.bmc.2021.116209] [Reference Citation Analysis]
17 Sofan MA, El‐mekabaty A, Hasel AM, Said SB. Synthesis, cytotoxicity assessment and antioxidant activity of some new thiazol‐2‐yl carboxamides. J Heterocyclic Chem 2021;58:1645-55. [DOI: 10.1002/jhet.4301] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
18 Zhao Z, Wang Y, Tian N, Yan H, Wang J. Synthesis and biological evaluation of N 6 derivatives of 8-azapurine as novel antiplatelet agents. RSC Med Chem 2021;12:1414-27. [PMID: 34458743 DOI: 10.1039/d1md00128k] [Reference Citation Analysis]
19 Song X, Zhu X, Li T, Liang C, Zhang M, Shao Y, Tao J, Sun R. Dehydrozingerone Inspired Discovery of Potential Broad-Spectrum Fungicidal Agents as Ergosterol Biosynthesis Inhibitors. J Agric Food Chem 2019;67:11354-63. [DOI: 10.1021/acs.jafc.9b04231] [Cited by in Crossref: 10] [Cited by in F6Publishing: 5] [Article Influence: 3.3] [Reference Citation Analysis]
20 Liu J, Huang H, Deng X, Xiong R, Cao X, Tang G, Wu X, Xu S, Peng J. Design, synthesis and broad-spectrum Bcr-Abl inhibitory activity of novel thiazolamide–benzamide derivatives. RSC Adv 2019;9:2092-101. [DOI: 10.1039/c8ra10096a] [Cited by in Crossref: 3] [Article Influence: 1.0] [Reference Citation Analysis]
21 Pham VH, Phan TPD, Phan DC, Vu BD. Synthesis and Bioactivity of Hydrazide-Hydrazones with the 1-Adamantyl-Carbonyl Moiety. Molecules 2019;24:E4000. [PMID: 31694218 DOI: 10.3390/molecules24214000] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 2.3] [Reference Citation Analysis]
22 Çıkla-Süzgün P, Küçükgüzel ŞG. Recent Advances in Apoptosis: THE Role of Hydrazones. Mini Rev Med Chem 2019;19:1427-42. [PMID: 30968776 DOI: 10.2174/1389557519666190410125910] [Cited by in Crossref: 3] [Cited by in F6Publishing: 5] [Article Influence: 1.0] [Reference Citation Analysis]
23 Sharma PC, Bansal KK, Sharma A, Sharma D, Deep A. Thiazole-containing compounds as therapeutic targets for cancer therapy. Eur J Med Chem 2020;188:112016. [PMID: 31926469 DOI: 10.1016/j.ejmech.2019.112016] [Cited by in Crossref: 60] [Cited by in F6Publishing: 30] [Article Influence: 20.0] [Reference Citation Analysis]
24 Alizadeh-bami F, Mehrabi H, Ranjbar-karimi R. One-pot three-component reaction of arylglyoxals with acetylthiourea and Meldrum’s acid or barbituric acid for synthesis of new 2-acetamido-4-arylthiazol-5-yl derivatives. Journal of Sulfur Chemistry 2019;40:469-78. [DOI: 10.1080/17415993.2019.1602127] [Cited by in Crossref: 6] [Article Influence: 2.0] [Reference Citation Analysis]
25 Guan Z, Liu Z, Wan Q, Ding M. One-pot four-component synthesis of polysubstituted thiazoles via cascade Ugi/Wittig cyclization starting from odorless Isocyano(triphenylphosphoranylidene)-acetates. Tetrahedron 2020;76:131101. [DOI: 10.1016/j.tet.2020.131101] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 2.5] [Reference Citation Analysis]
26 Govindaiah P, Dumala N, Mattan I, Grover P, Jaya Prakash M. Design, synthesis, biological and in silico evaluation of coumarin-hydrazone derivatives as tubulin targeted antiproliferative agents. Bioorganic Chemistry 2019;91:103143. [DOI: 10.1016/j.bioorg.2019.103143] [Cited by in Crossref: 8] [Cited by in F6Publishing: 6] [Article Influence: 2.7] [Reference Citation Analysis]
27 Wazalwar SS, Banpurkar AR, Perdih F. Single crystal structure of 3-(2-(3-acetylphenyl)hydrazono)pentane-2,4-dione and molecular docking study with CYP450 members for anticancer molecular screening. Journal of the Indian Chemical Society 2022;99:100482. [DOI: 10.1016/j.jics.2022.100482] [Reference Citation Analysis]
28 Jaita S, Phakhodee W, Chairungsi N, Pattarawarapan M. Mechanochemical synthesis of primary amides from carboxylic acids using TCT/NH4SCN. Tetrahedron Letters 2018;59:3571-3. [DOI: 10.1016/j.tetlet.2018.08.035] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 1.3] [Reference Citation Analysis]
29 Popiołek Ł, Piątkowska-Chmiel I, Gawrońska-Grzywacz M, Biernasiuk A, Izdebska M, Herbet M, Sysa M, Malm A, Dudka J, Wujec M. New hydrazide-hydrazones and 1,3-thiazolidin-4-ones with 3-hydroxy-2-naphthoic moiety: Synthesis, in vitro and in vivo studies. Biomed Pharmacother 2018;103:1337-47. [PMID: 29864916 DOI: 10.1016/j.biopha.2018.04.163] [Cited by in Crossref: 13] [Cited by in F6Publishing: 9] [Article Influence: 3.3] [Reference Citation Analysis]
30 Tok F, Ilhan R, Günal S, Ballar-Kirmizibayrak P, Koçyiğit-Kaymakçioğlu B. Design, Synthesis and Evaluation of the Biological Activities of Some New Carbohydrazide and Urea Derivatives. Turk J Pharm Sci 2018;15:304-8. [PMID: 32454674 DOI: 10.4274/tjps.64935] [Reference Citation Analysis]
31 Mohareb RM, Abdallah AEM, Ahmed EA. Synthesis and cytotoxicity evaluation of thiazole derivatives obtained from 2-amino-4,5,6,7-tetrahydrobenzo[b]thiophene- 3-carbonitrile. Acta Pharm 2017;67:495-510. [PMID: 29337677 DOI: 10.1515/acph-2017-0040] [Cited by in Crossref: 11] [Cited by in F6Publishing: 7] [Article Influence: 2.8] [Reference Citation Analysis]
32 Duhan M, Singh R, Devi M, Sindhu J, Bhatia R, Kumar A, Kumar P. Synthesis, molecular docking and QSAR study of thiazole clubbed pyrazole hybrid as α-amylase inhibitor. Journal of Biomolecular Structure and Dynamics 2021;39:91-107. [DOI: 10.1080/07391102.2019.1704885] [Cited by in Crossref: 20] [Cited by in F6Publishing: 12] [Article Influence: 6.7] [Reference Citation Analysis]
33 Wu Z, Ding N, Tang Y, Ye J, Peng J, Hu A. Synthesis and antitumor activity of novel N-(5-benzyl-4-(tert-butyl)thiazol-2-yl)-2-(piperazin-1-yl)acetamides. Res Chem Intermed 2017;43:4833-50. [DOI: 10.1007/s11164-017-2915-6] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
34 Ayati A, Emami S, Moghimi S, Foroumadi A. Thiazole in the targeted anticancer drug discovery. Future Medicinal Chemistry 2019;11:1929-52. [DOI: 10.4155/fmc-2018-0416] [Cited by in Crossref: 26] [Cited by in F6Publishing: 15] [Article Influence: 8.7] [Reference Citation Analysis]
35 Popiołek Ł, Biernasiuk A. Synthesis and investigation of antimicrobial activities of nitrofurazone analogues containing hydrazide-hydrazone moiety. Saudi Pharm J 2017;25:1097-102. [PMID: 29158722 DOI: 10.1016/j.jsps.2017.05.006] [Cited by in Crossref: 20] [Cited by in F6Publishing: 14] [Article Influence: 4.0] [Reference Citation Analysis]
36 Kim YJ, Kwon HJ, Han SY, Gong YD. Synthesis of 2-Amino-5-Carboxamide Thiazole Derivatives via Dehydrative Cyclization of Thiourea Intermediate Resin on Solid Phase. ACS Comb Sci 2019;21:380-8. [PMID: 30848875 DOI: 10.1021/acscombsci.9b00001] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
37 Popiołek Ł, Biernasiuk A. New Hydrazides and Hydrazide-Hydrazones of 2,3-Dihalogen Substituted Propionic Acids: Synthesis and in vitro Antimicrobial Activity Evaluation. Chem Biodivers 2017;14. [PMID: 28444991 DOI: 10.1002/cbdv.201700075] [Cited by in Crossref: 6] [Cited by in F6Publishing: 3] [Article Influence: 1.2] [Reference Citation Analysis]
38 Hassan AA, Mohamed NK, Aly AA, Tawfeek HN, Bräse S, Nieger M. Synthesis and crystallographic evaluation of diazenyl- and hydrazothiazoles. [5.5] sigmatropic rearrangement and formation of thiazolium bromide dihydrate derivatives. Journal of Molecular Structure 2019;1176:346-56. [DOI: 10.1016/j.molstruc.2018.08.106] [Cited by in Crossref: 6] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
39 Khattab TA. From chromic switchable hydrazones to smart materials. Materials Chemistry and Physics 2020;254:123456. [DOI: 10.1016/j.matchemphys.2020.123456] [Cited by in Crossref: 22] [Cited by in F6Publishing: 7] [Article Influence: 11.0] [Reference Citation Analysis]
40 Peng H, Ye L, Zhang M, Yang Y, Zheng J. Synthesis and antimicrobial activity of 3,4-dihydropyrimidin-2(1H)-one derivatives containing a hydrazone moiety. Heterocyclic Communications 2018;24:113-7. [DOI: 10.1515/hc-2017-0227] [Cited by in Crossref: 4] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
41 Shareef MA, Devi GP, Rani Routhu S, Kumar CG, Kamal A, Babu BN. New imidazo[2,1-b]thiazole-based aryl hydrazones: unravelling their synthesis and antiproliferative and apoptosis-inducing potential. RSC Med Chem 2020;11:1178-84. [PMID: 33479622 DOI: 10.1039/d0md00188k] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
42 Krishnan KG, Ashothai P, Padmavathy K, Lim W, Mai C, Thanikachalam PV, Ramalingan C. Hydrazide-integrated carbazoles: synthesis, computational, anticancer and molecular docking studies. New J Chem 2019;43:12069-77. [DOI: 10.1039/c9nj01912j] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
43 Zhao Z, Wang H, Tian N, Yan H, Wang J. Synthesis and biological evaluation of N4 -hydrazone derivatives of 5,7-dihydro-6H-pyrrolo[2,3-d]pyrimidin-6-one as novel anticancer agents with antimetastatic adjunct efficacy. Arch Pharm (Weinheim) 2021;:e2100213. [PMID: 34368988 DOI: 10.1002/ardp.202100213] [Reference Citation Analysis]
44 Wan Y, Long J, Gao H, Tang Z. 2-Aminothiazole: A privileged scaffold for the discovery of anti-cancer agents. Eur J Med Chem 2021;210:112953. [PMID: 33148490 DOI: 10.1016/j.ejmech.2020.112953] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]