Yıl: 2020 Cilt: 44 Sayı: 4 Sayfa Aralığı: 1164 - 1176 Metin Dili: İngilizce DOI: 10.3906/kim-2004-78 İndeks Tarihi: 22-06-2022

Bis benzothiophene Schiff bases: synthesis and in silico-guided biological activity studies

Öz:
Since benzo [ b ] thiophene scaffold is one of the privileged structures in drug discovery as this core exhibitsactivities for different biological problems, in this study bis (benzo[ b ]thiophene-2-yl) alkyl methanimine derivatives (1-9) were synthesized by reacting benzo[ b ]thiophene-2-carbaldehyde with diamines. All newly compounds were characterized by IR, $^{1}H$ NMR and $^{13} C NMR$ spectroscopic methods. Synthesized compounds were investigated using binary QSARbased models on therapeutic activity prediction of synthesized compounds and they showed high predicted activities in following diseases: bacterial, angina, allergy, depression and obesity. Thus, they were then tested for their antimicrobial and antileishmanial activities as a result of this theoretical study. Compound 1(N, N’- (propane-1,3-diyl) bis (1-(benzo [ b ] thiophene-2-yl)) methanimine) was found the most active compound in both diseases. Thus, its molecular docking studies were also carried out.
Anahtar Kelime:

Belge Türü: Makale Makale Türü: Araştırma Makalesi Erişim Türü: Erişime Açık
  • 1. Rangappa SK, Karam C, Srinivasa B, Sasidhar BS, Siddappa AP et al. An overview of benzo[b]thiophene-based medicinal chemistry. European Journal of Medicinal Chemistry 2017; 138: 1002-1033. doi: 10.1016/j.ejmech.2017.07.038
  • 2. Jagtap VA, Agasimundin YS. Synthesis and preliminary evaluation of some 2-amino-n’-[substituted]-4,5,6,7- tetrahydro-1-benzothiophene-3- carbohydrazide as antimicrobial agents. Journal of Pharmacy Research 2015; 9 (1): 10-14.
  • 3. Berrade L, Aisa B, Ramirez MJ, Galiano S, Guccione S et al. Novel benzo[b]thiophene derivatives as new potential antidepressants with rapid onset of action. European Journal of Medicinal Chemistry 2011; 54: 3086-3090. doi: 10.1021/jm001059j
  • 4. Lianqi JL, Kai G, Na LV. Benzothiophene Alkanol Piperazine Derivatives and Their Use as Antidepressant, WO Patent 2010/000198 A1.
  • 5. Bryant HU, Dere WH. Selective estrogen receptor modulators: an alternative to hormone replacement therapy.Society for Experimental Biology and Medicine 1998; 217 (1): 45-52. doi: 0.3181/00379727-217-44204
  • 6. Rao GK, Subramaniam, R. Synthesis, antitubercular and antibacterial activities of some quinazolinone analogs substituted with benzothiophene. Journal of Chemical Sciences 2015; 6: 92-96. doi: 10.4172/2150-3494.100092
  • 7. Yang Y, Cui M. Radiolabeled bioactive benzoheterocycles for imaging bamyloid plaques in Alzheimer’s diseas. European Journal of Medicinal Chemistry 2014; 87: 703-721. doi: 10.1016/j.ejmech.2014.10.012
  • 8. Pettit GR, Minardi MD, Boyd MR, Pettit RK. Synthesis of combretastatin A-3 diphosphate prodrug. Anticancer Drugs Design 2000; 15 (6): 397-403.
  • 9. Pettit GR, Lippert JW. Antineoplastic agents 429. Syntheses of the combretastatin A-1 and combretastatin B-1 prodrug. Anticancer Drug Design 2000; 15 (3): 203-216.
  • 10. Ünver Y, Deniz S, Çelik F, Akar Z, Küçük M et al. Synthesis of new 1,2,4-triazole compounds containing Schiff and Mannich bases (morpholine) with antioxidant and antimicrobial activities. Journal of Enzym Inhibition and Medicinal Chemistry 2016; 31(Sup 3): 89-95. doi: 10.1080/14756366.2016.1206088
  • 11. Ünver Y, Sancak K, Çelik F, Birinci E, Küçük, M. New thiophene-1,2,4-triazole-5(3)-ones: highly bioactive thiosemicarbazides, structures of Schiff bases and triazole-thiols. European Journal of Medicinal Chemistry 2014; 84: 639-650. doi: 10.1016/j.ejmech.2014.01.014
  • 12. Ünver Y, Bektaş E. Synthesis and biological activity of new Schiff bases of benzylideneamine bearing thiophene, 1,2,4-triazolone, 1,3,4-oxadiazole, morpholine moieties. Letters in Drug Design & Discovery 2018; 15 (7): 706-712. doi: 10.2174/1570180814666171012163651
  • 13. Da Silva CM, Da Silva DL, Modolo LV, Alves RB, De Resende MA et al. Schiff base: a short review of their antimicrobial activities. Journal of Advanced Research 2011; 2 (1): 1-8. doi: 10.1016/j.jare.2010.05.004
  • 14. Khurshid IM, Mustakim M, Vasudevan S, Madhubhai MP, Syed MA et al. Synthesis, anti-inflammatuar, analgesic and antioxidant activities of some tetrasubstituted thiophenes. Journal of Enzyme Inhibition and Medicinal Chemistry 2008; 23 (6): 829-838. doi: 10.1080/14756360701626082.
  • 15. Ravi K, Airody V, James PS. A new class of antionulsants possessing 6Hz activity: 3,4-dialkyloxy thiophene bishydrazones. European Journal of Medicinal Chemistry 2009; 44 (11): 4376-4384. doi: 10.1016/j.ejmech.2009.05.026.
  • 16. Daver M, Boghaei MS. Non-symmetrical tetradentate vanadyl Schiff base complexes derived from 1,2-phKM, nylene diamine and 1,3-naphtalene diamine as catalysts for the oxidation of cyclohexene. Tetrahedron 2002; 58 (26): 5357-5366. doi: 10.1016/S0040-4020(02)00481-7.
  • 17. Vyas KM, Jadeja N, Gupta VK, Surati KR. Synthesis, characterization and crystal structure of some bidentate heterocyclic Schiff base ligands of 4-toluoyl-pyrazolones and its mononuclear Cu(II) complex. Journal of Molecular Structure 2011; 990 (1-3): 110-120. doi: 10.1016/j.molstruc.2011.01.024
  • 18. Jiang JJ, Chang TC, Hsu WL, Hwang JM, Hsu LY. Synthesis and biological activity of sulfur containing arylaldehyde Schiff bases. Chemical Pharmaceutical Bulletin 2003; 51 (11): 1307-1310. doi: 10.1248/cpb.51.1307
  • 19. Jiang Q, Chen J, Yang C, Yin Y, Yao K. Quorum sensing: a prospective therapeutic target for bacterial diseases. BioMed Research International 2019; 2019: 1-15. doi: 10.1155/2019/2015978
  • 20. Yadav PS, Senthilkumar GP. Synthesis and evaluation of some benzothiazole derivatives as antidiabetic agents. International Journal of PharmTech Research 2011; 3 (1): 1-7.
  • 21. Şener S, Karaman Ü, Hakverdi G, Saraç G, Kayhan Tetik B. Evaluation of patients with cutaneous leishmaniasis who admitted to dermatology clinic in Kahramanmaraş Sütçü İmam University Medical Faculty. Konuralp Tıp Dergisi 2017; 9 (3): 274-277.
  • 22. Özbilgin A, Harman M, Karakuş A, Bart M, S. Töz S et al. Leishmaniasis in Turkey: visceral and cutaneous leishmaniasis caused by Leishmania donovani in Turkey. Acta Tropica 2017; 173: 90-96.
  • 23. Schrödinger Release LigPrep LLC. New York, NY, USA, 2015.
  • 24. Banks JL, Beard HS, Cao Y, Cho AE, W. Damm W et al. Integrated modeling program, applied chemical theory (IMPACT). Journal of Computational Chemistry 2005; 26 (16): 1752-1780. doi: 10.1002/jcc.20292
  • 25. Shelley JC, Cholleti A, Frye LL, Greenwood JR, Timlin MR et al. Epik: a software program for pKa prediction and protonation state generation for drug-like molecules. Journal of Computer-Aided Molecular Design 2007; 21: 681-691.
  • 26. Sastry GM, Adzhigirey M, Day T, Annabhimoju R, Sherman W. Protein and ligand preparation: parameters, protocols, and influence on virtual screening enrichments. Journal of Computer-Aided Molecular Design 2013; 27: 221-234.
  • 27. Bas DC, Rogers DM, Jensen JH. Very fast prediction and rationalization of pKa values for protein–ligand complexes. Proteins: Structure, Function, and Bioinformatics 2008; 73: 765-783.
  • 28. Li H, Robertson AD, Jensen JH. Very fast empirical prediction and rationalization of protein pKa values. Proteins: Structure, Function, and Bioinformatics 2005; 61: 704-721.
  • 29. Friesner RA, Murphy RB, Repasky MP, Frye LL, Greenwood JR et al. Extra precision glide: docking and scoring incorporating a model of hydrophobic enclosure for protein-ligand complexes. Journal of Medicinal Chemistry 2006; 49 (21): 6177-6196. doi: 10.1021/jm051256o
  • 30. Maina ENM, Njau VN, Gavamukulya Y. Phytochemical analysis and antileishmanial activity of Clerodendrum myricoides and Salvadora persica plant extracts against Leishmania major. Journal of Complementary and Alternative Medical Research 2020; 9 (1): 29-44. doi: 10.9734/jocamr/2020/v9i130134
  • 31. Ogeto TK, Odhiambo RA, Shivairo RS, Muleke CI, Osero BO et al. Antileishmanial activity of Aloe secundiflora plant extracts against Leishmania major. Advances in Life Science and Technology 2013; 13: 9-19.
APA ÜNVER Y, Ünlüer D, Direkel Ş, Durdagi S (2020). Bis benzothiophene Schiff bases: synthesis and in silico-guided biological activity studies. , 1164 - 1176. 10.3906/kim-2004-78
Chicago ÜNVER YASEMİN,Ünlüer Dilek,Direkel Şahin,Durdagi Serdar Bis benzothiophene Schiff bases: synthesis and in silico-guided biological activity studies. (2020): 1164 - 1176. 10.3906/kim-2004-78
MLA ÜNVER YASEMİN,Ünlüer Dilek,Direkel Şahin,Durdagi Serdar Bis benzothiophene Schiff bases: synthesis and in silico-guided biological activity studies. , 2020, ss.1164 - 1176. 10.3906/kim-2004-78
AMA ÜNVER Y,Ünlüer D,Direkel Ş,Durdagi S Bis benzothiophene Schiff bases: synthesis and in silico-guided biological activity studies. . 2020; 1164 - 1176. 10.3906/kim-2004-78
Vancouver ÜNVER Y,Ünlüer D,Direkel Ş,Durdagi S Bis benzothiophene Schiff bases: synthesis and in silico-guided biological activity studies. . 2020; 1164 - 1176. 10.3906/kim-2004-78
IEEE ÜNVER Y,Ünlüer D,Direkel Ş,Durdagi S "Bis benzothiophene Schiff bases: synthesis and in silico-guided biological activity studies." , ss.1164 - 1176, 2020. 10.3906/kim-2004-78
ISNAD ÜNVER, YASEMİN vd. "Bis benzothiophene Schiff bases: synthesis and in silico-guided biological activity studies". (2020), 1164-1176. https://doi.org/10.3906/kim-2004-78
APA ÜNVER Y, Ünlüer D, Direkel Ş, Durdagi S (2020). Bis benzothiophene Schiff bases: synthesis and in silico-guided biological activity studies. Turkish Journal of Chemistry, 44(4), 1164 - 1176. 10.3906/kim-2004-78
Chicago ÜNVER YASEMİN,Ünlüer Dilek,Direkel Şahin,Durdagi Serdar Bis benzothiophene Schiff bases: synthesis and in silico-guided biological activity studies. Turkish Journal of Chemistry 44, no.4 (2020): 1164 - 1176. 10.3906/kim-2004-78
MLA ÜNVER YASEMİN,Ünlüer Dilek,Direkel Şahin,Durdagi Serdar Bis benzothiophene Schiff bases: synthesis and in silico-guided biological activity studies. Turkish Journal of Chemistry, vol.44, no.4, 2020, ss.1164 - 1176. 10.3906/kim-2004-78
AMA ÜNVER Y,Ünlüer D,Direkel Ş,Durdagi S Bis benzothiophene Schiff bases: synthesis and in silico-guided biological activity studies. Turkish Journal of Chemistry. 2020; 44(4): 1164 - 1176. 10.3906/kim-2004-78
Vancouver ÜNVER Y,Ünlüer D,Direkel Ş,Durdagi S Bis benzothiophene Schiff bases: synthesis and in silico-guided biological activity studies. Turkish Journal of Chemistry. 2020; 44(4): 1164 - 1176. 10.3906/kim-2004-78
IEEE ÜNVER Y,Ünlüer D,Direkel Ş,Durdagi S "Bis benzothiophene Schiff bases: synthesis and in silico-guided biological activity studies." Turkish Journal of Chemistry, 44, ss.1164 - 1176, 2020. 10.3906/kim-2004-78
ISNAD ÜNVER, YASEMİN vd. "Bis benzothiophene Schiff bases: synthesis and in silico-guided biological activity studies". Turkish Journal of Chemistry 44/4 (2020), 1164-1176. https://doi.org/10.3906/kim-2004-78