References
1. Rahul.D.K, Rohan.J.M, Shrikant.V. H, Rahul.A.M, Sonali.S.K, Rajesh.N.G, et al. Synthesis and in silico investigation of thiazoles bearing pyrazoles derivatives as anti-inflammatory agents. Comp. Biol. Chem 2016; 61:86-96.
2. Satish.K, Deepika.R.K.C, Sreenivas.A, Jayaram.R.K, Srigiridhar.K, Rambabu.Y. Synthesis and anticancer evaluation of 3-aryl-6-phenylimidazo [2,1-b]thiazoles. Bioorg. Med. Chem. Lett 2014; 24:5428-5431.
3. Carlos Nava.Z, Fabiola.C, Rosa.M, Manuel.J.C, Benjamin.O.M, Hermene-gilda. M.D, et al.. 2-Acylamino-5-nitro-1,3-thiazoles: Preparation and in vitro bioevaluation against four neglected protozoan parasites. Bioorg. Med. Chem 2014; 22:1626-1633.
4. Aldo.A, Alberto.L, Alessandra.L, Rita.M, Mirella.R, Rinaldo.C et al. Thiazoles. Eur. J. Med. Chem 2013; 68:412-421.
5. Nataliya.Z, Dmytro.A, Olexandr.V, Philippe.G, Roman.L. Thiazoles. Bioorg. Med. Chem. Lett 2012; 22:7071-7074.
6. Belem.A, Aaron.R, Heather.S, Donard .S.D, Mark.J.K. Triazolbenzo[d]thiazoles: Efficient synthesis and biological evalua-tion as neuroprotective agents , Bioorg. Med. Chem. Lett 2012; 22:5976-5978.
7. Maria.I.L.S, Ana.F.B, Mafalda.L, Jose. A.P, Filomena.M.B, Teresa.M.V.D, et al. Chiral 6,7-bis(hydroxymethyl)-1H,3H-pyrrolo[1,2-c]thiazoles with anti-breast cancer properties . Eur. J. Med. Chem 2013; 60: 254-262.
8. Nareshvarma.S, Shrivastava.S.P. Synthesis and in vitro study of [1,3,4]thiadiazol-2yl-3,3a,5,6-tetrahydro-2H-pyrazolo[3,4-d]thiazoles as antimicrobial agents Journal of Saudi Chemical Society 2016;20:33-39.
9. Shahenda.M. E, Ghada.S.H, Fatmah.A.M. A, Hussein.I.E. Substituted thiazoles VI. Synthesis and antitumor activity of new 2-acetamido- and 2 or 3-propanamido-thiazoleanalogs. Eur. J. Med. Chem.Volume 2012; 54:615-625.
10. Ghada.S.H, Shahenda.M.E, Fatmah. A.M.A, Hussein.I.E. Substituted thiazoles VII. Synthesis and antitumor activity of certain 2-(substituted amino)-4-phenyl-1,3-thiazole analogs, Bioorg. Med. Chem. Lett 2012; 22:6318-6323.
11. Kalkhambkar.R.G, Kulkarni.G.M, Shivkumar. H, Nagendra.R.R. Synthesis of novel triheterocyclic thiazoles as anti-inflammatory and analgesic agents , Eur. J. Med. Chem 2007; 42:1272-1276.
12. Nadee.S, Waquar.A. Triazole incorporated thiazoles as a new class of anticonvulsants: Design, synthesis and in vivo screening. Eur. J. Med. Chem 2010; 45:1536-1543.
13. Nathan.A, Axerio.C.P, Tavassoli, Peyman, Han, Frank.Q, et al. Targeting the Binding Function 3 (BF3) Site of the Human Androgen Receptor through Virtual Screening. J. Med. Chem 2011; 54:8563-8573.
14. Garcia-Domenech, Ramon, Barbosa, Luciana, Lacarra, Matilde, et al. Application of molecular topology to predict the inhibition of Trypanosoma cruzi cruzain by thiosemicarbazones. J. Mol.Design 2008; 7:260-272.
15. Cohen, Fred.E, Du, Xiaohui.G , Chun, Mckerrow, James H. Preparation of thiosemicarbazones and semicarbazones as inhibitors of cysteine proteases and methods of their use. U.S. Pat. Appl. Publ. 2004, US 20040014801 A120040122.
16. Du, Xiaohu, Guo, Chun, Hansell, Elizabeth, et al. Synthesis and Structure-Activity Relationship Study of Potent Trypanocidal Thio Semicarbazone Inhibitors of the Trypanosomal Cysteine Protease Cruzain. J. Med. Chem 2002; 45:2695-2707.
17. Zee-Cheng, Kwang.Y, Nyberg, Wayne.H, Cheng.C.C. Synthesis of 8,9-dialkoxy-substituted tetrahydrobenz[h]isoquinoline-s. J. Heterocyclic Chem 1972; 9: 805-11.
18. Du, Xiaohui. Synthesis and Structure-Activity Relationship Study of Potent Trypanocidal Thio Semicarbazone Inhibitors of the Trypanosomal Cysteine Protease Cruzain. J. Med. Chem 2002; 45:2695-2707.
19. Cohen, Fred. E. Preparation of thiosemicarbazones and semicarbazones as inhibitors of cysteine proteases and methods of their use. U.S. Pat. Appl. Publ.20040014801, 2004.