Araştırma Makalesi
Yıl 2023,
Cilt: 2 Sayı: 2, 71 - 77, 28.08.2023
Öz
Destekleyen Kurum
Anadolu Üniversitesi
Proje Numarası
1404S116
Kaynakça
- Parihar, MS., Hemnani T. Alzheimer’s disease pathogenesis and therapeutic interventions. J Clin Neurosci. (2004); 11(5):456-467. https://doi.org/10.1016/j.jocn.2003.12.007
- Thacker P.D. Surpising discovery with alzheimer’s medication. Drug Discovery Today. (2003) 1, 8- 9. https://doi.org/10.1016/S1359-6446(03)02685-0
- Yamada K., Takayagani M., Kamei H., Nagai T., Dohniwa M., Kobayashi K., Ohhara T., Takauma K., Nabeshima T. Effects of memantine and donepezil on amyloid β-induced memory impairment in a delayed-matching to position task in rats. Behav Brain Resb. (2005);162(2):191-9. https://doi.org/10.1016/j.bbr.2005.02.036
- Rösler M, Anand R, Cicin-Sain A, Gauthier S, Agid Y, Dal-Bianco P, Stähelin H B, Hartman R, Gharabawi M. Efficacy and safety of rivastigmine in patients with Alzheimer’s disease: international randomised controlled trial. British Medical Journal. (1999);318(7184):633-8. https://doi.org/10.1136/bmj.318.7184.633
- Racci, M., Mazzucchelli, M., Porello, E., Lanni, C., Govoni, S. Acetylcholinesterase inhibitors: novel activities of old molecules, Pharm Res. (2004); 50;441-451. https://doi.org/10.1016/j.phrs.2003.12.027
- Jann, M.W., Shirley, K.L., Small, G.W. Cinical pharmacokinetics and pharmacodynamics of cholinesterase inhibitors. Clin Pharmacokinet. (2002);41, 10, 719-739. https://doi.org/10.2165/00003088-200241100-00003
- Clarissa M Comim 1, Josimar G Pereira, Amanda Steckert, Fabrícia Petronilho, Tatiana Barichello, João Quevedo, Felipe Dal-Pizzol. Rivastigmine reverses habituation memory impairment observed in sepsis survivor rats. Shock. (2009);32(3):270-1. https://doi.org/10.1097/SHK.0b013e31819963c4
- Şahin H.A. Asetilkolin, kolinesterazlar ve alzheimer hastalığı, Demans Dergisi. (2002); 2:69-73.
- David G., Wilkinson P.T., Schwam E., Parrish J.P. Cholinesterase inhibitors used in the treatment of alzheimer’s disease. the relationship between pharmacological effects and clinical efficacy, Drugs Aging. (2004):21(7): 453-478. https://doi.org/10.2165/00002512-200421070-00004
- Neşe Ç. Butrylcholinesterase: Structure And Physiological Importance. Turk J Biochem. (2003); 28(2):54-61. https://doi.org/10.1046/j.1365-3032.2003.00314.x
- Ha ZY, Ong HC, Oo CW, Yeong KY. Synthesis, Molecular Docking, and Biological Evaluation of Benzimidazole Derivatives as Selective Butyrylcholinesterase Inhibitors. Curr Alzheimer Res. (2020);17(13):1177-1185. https://doi.org/10.2174/1567205018666210218151228
- Demirayak S, Kayagil I, Yurttas L. Microwave supported synthesis of some novel 1,3-Diarylpyrazino[1,2-a]benzimidazole derivatives and investigation of their anticancer activities. Eur J Med Chem. (2011);46:411-416. https://doi.org/10.1016/j.ejmech.2010.11.007
- Yurttaş L, Demirayak S, Akalın Çiftci G, Yıldırım ŞU, Kaplancıklı ZA. Synthesis and biological evaluation of some 1,2-disubstituted benzimidazole derivatives as new potential anticancer agents. Arch Pharm Chem Life Sci. (2013);346:403-414. https://doi.org/10.1002/ardp.201200452
- Chawla A, Ramandeep K, Goyal A. Importance of microwave reactions in the synthesis of novel benzimidazole derivatives: A review. J Chem Pharm Res. 2011;3:925-944.
- Husain A, Rashid M, Mishra R, Parveen S, Shin DS, Kum D. Benzimidazole bearing oxadiazole and triazolo-thiadiazoles nucleus: Design and synthesis as anticancer agents. Bioorg Med Chem Lett. 2012;22:5438-5444. https://doi.org/10.1016/j.bmcl.2012.07.038
- Alpan AS, Parlar S, Carlino I, Tarikgullari AH, Alptüzün V, Günes HS. Synthesis, biological activity and molecular modeling studies on 1H-benzimidazole derivatives as acetylcholinesterase inhibitors. Bioorg. Med. Chem. (2013);21(17):4928-37. https://doi.org/10.1016/j.bmc.2013.06.065
- Surve P, Ravindran S, Acharjee A, Rastogi H, Basu S, Honrao P. Metabolite characterization of anti-cancer agent Gefitinib in human hepatocytes. Drug Metab Lett. (2013);7:126-136. https://doi.org/10.2174/1872312808666140317154110
- Akalın Çiftçi G, Temel HE, Yurttaş L. Apoptotic Effect of Novel Benzimidazole Derivatives Bearing Pyridyl/Pyrimidinyl Piperazine Moiety. Anti-Cancer Agents Med. Chem., (2022);22:1780-1792. https://doi.org/10.2174/1871520621666210708095110
- Ellman G.L., Courtney K.D., Anders V., Featherstone R.M. A New And Rapid Colorimetric Determination Of Acetylcholinesterase Activity. Biochem. Pharmacol. (1961);7:88-95. https://doi.org/10.1016/0006-2952(61)90145-9
- Mosmann T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J Immunol Methods. (1983);65,(1-2):55-63. https://doi.org/10.1016/0022-1759(83)90303-4
- Keiser K., Johnson C.C., Tipton D.A. Cytotoxicity of mineral trioxide aggregate using human periodontal ligament fibroblasts. Journal of Endodontics. (2000); 26: 288-291. https://doi.org/10.1097/00004770-200005000-00010
- Yurttaş L, Ozkay Y, Demirci F, Göger G, Ulusoylar-Yıldırım Ş, Abu Mohsen U, Öztürk Ö, Kaplancıklı ZA. Synthesis, anticandidal activity, and cytotoxicity of some thiazole derivatives with dithiocarbamate side chains, Turk J Chem. (2014);38:815-824. https://doi.org/10.3906/kim-1312-62
- Ji F, Fengqi B, MinGu, Jing L, Zhipeng Z, Jiaoli D, Sai-Sai X and Jinsong D. Design, synthesis and evaluation of quinolinone derivatives containing dithiocarbamate moiety as multifunctional AChE inhibitors for the treatmentof Alzheimer’s disease, J Enzyme Inhib Med Chem. (2020);35:118-128. https://doi.org/10.1080/14756366.2019.1687460
- Honghua Z, Yuying W, Yuqing W, Xuelin L, Şuji W, Zhen W. Recent advance on carbamate-based cholinesterase inhibitors as potential multifunctional agents against Alzheimer’s disease, Eur J Med Chem. (2022); 240:114606. https://doi.org/10.1016/j.ejmech.2022.114606
Screening of new morpholine dithiocarbamate derivatives bearing benzimidazole moiety for anticholinesterase potential
Öz
Alzheimer’s disease (AD) is basically associated with disturbances of cholinesterase metabolism which result in acetylcholine deficiency. Target of acetylcholinesterase (AChE) inhibitors used in symptomatic therapy of disease is to increase of ACh levels. Consequently, cholinesterase inhibitors were developed to increase acetylcholine is to inhibit AChE and butrylcholinesterase (BuChE). Studies demonstrate the clinical importance of dual inhibitors that inhibit not only the acetylcholinesterase enzyme but also the butyrylcholinesterase enzyme.
In recent years, benzimidazoles have attracted particular interest owing to their anticolinesterase activity. In this manner, we have synthesized benzimidazole and morpholine including compounds (2a-i). Final compounds were achieved with the reaction of (benzimidazol-2-yl) methyl morpholine-4-carbodithioate and α-bromoacetophenone derivatives in acetone at room temperature with stirring. Inhibition effects of novel morpholine dithiocarbamates (2a-i) were tested on AChE and BuChE. Compound 2d demonstrated dual inhibitory activity on AChE and BuChE (78±1,56, 70,71±1,53, respectively), with the lowest cytotoxicity to normal cell line.
Anahtar Kelimeler
Acetylcholinesterase butrylcholinesterase Alzheimer benzimidazole
Proje Numarası
1404S116
Kaynakça
- Parihar, MS., Hemnani T. Alzheimer’s disease pathogenesis and therapeutic interventions. J Clin Neurosci. (2004); 11(5):456-467. https://doi.org/10.1016/j.jocn.2003.12.007
- Thacker P.D. Surpising discovery with alzheimer’s medication. Drug Discovery Today. (2003) 1, 8- 9. https://doi.org/10.1016/S1359-6446(03)02685-0
- Yamada K., Takayagani M., Kamei H., Nagai T., Dohniwa M., Kobayashi K., Ohhara T., Takauma K., Nabeshima T. Effects of memantine and donepezil on amyloid β-induced memory impairment in a delayed-matching to position task in rats. Behav Brain Resb. (2005);162(2):191-9. https://doi.org/10.1016/j.bbr.2005.02.036
- Rösler M, Anand R, Cicin-Sain A, Gauthier S, Agid Y, Dal-Bianco P, Stähelin H B, Hartman R, Gharabawi M. Efficacy and safety of rivastigmine in patients with Alzheimer’s disease: international randomised controlled trial. British Medical Journal. (1999);318(7184):633-8. https://doi.org/10.1136/bmj.318.7184.633
- Racci, M., Mazzucchelli, M., Porello, E., Lanni, C., Govoni, S. Acetylcholinesterase inhibitors: novel activities of old molecules, Pharm Res. (2004); 50;441-451. https://doi.org/10.1016/j.phrs.2003.12.027
- Jann, M.W., Shirley, K.L., Small, G.W. Cinical pharmacokinetics and pharmacodynamics of cholinesterase inhibitors. Clin Pharmacokinet. (2002);41, 10, 719-739. https://doi.org/10.2165/00003088-200241100-00003
- Clarissa M Comim 1, Josimar G Pereira, Amanda Steckert, Fabrícia Petronilho, Tatiana Barichello, João Quevedo, Felipe Dal-Pizzol. Rivastigmine reverses habituation memory impairment observed in sepsis survivor rats. Shock. (2009);32(3):270-1. https://doi.org/10.1097/SHK.0b013e31819963c4
- Şahin H.A. Asetilkolin, kolinesterazlar ve alzheimer hastalığı, Demans Dergisi. (2002); 2:69-73.
- David G., Wilkinson P.T., Schwam E., Parrish J.P. Cholinesterase inhibitors used in the treatment of alzheimer’s disease. the relationship between pharmacological effects and clinical efficacy, Drugs Aging. (2004):21(7): 453-478. https://doi.org/10.2165/00002512-200421070-00004
- Neşe Ç. Butrylcholinesterase: Structure And Physiological Importance. Turk J Biochem. (2003); 28(2):54-61. https://doi.org/10.1046/j.1365-3032.2003.00314.x
- Ha ZY, Ong HC, Oo CW, Yeong KY. Synthesis, Molecular Docking, and Biological Evaluation of Benzimidazole Derivatives as Selective Butyrylcholinesterase Inhibitors. Curr Alzheimer Res. (2020);17(13):1177-1185. https://doi.org/10.2174/1567205018666210218151228
- Demirayak S, Kayagil I, Yurttas L. Microwave supported synthesis of some novel 1,3-Diarylpyrazino[1,2-a]benzimidazole derivatives and investigation of their anticancer activities. Eur J Med Chem. (2011);46:411-416. https://doi.org/10.1016/j.ejmech.2010.11.007
- Yurttaş L, Demirayak S, Akalın Çiftci G, Yıldırım ŞU, Kaplancıklı ZA. Synthesis and biological evaluation of some 1,2-disubstituted benzimidazole derivatives as new potential anticancer agents. Arch Pharm Chem Life Sci. (2013);346:403-414. https://doi.org/10.1002/ardp.201200452
- Chawla A, Ramandeep K, Goyal A. Importance of microwave reactions in the synthesis of novel benzimidazole derivatives: A review. J Chem Pharm Res. 2011;3:925-944.
- Husain A, Rashid M, Mishra R, Parveen S, Shin DS, Kum D. Benzimidazole bearing oxadiazole and triazolo-thiadiazoles nucleus: Design and synthesis as anticancer agents. Bioorg Med Chem Lett. 2012;22:5438-5444. https://doi.org/10.1016/j.bmcl.2012.07.038
- Alpan AS, Parlar S, Carlino I, Tarikgullari AH, Alptüzün V, Günes HS. Synthesis, biological activity and molecular modeling studies on 1H-benzimidazole derivatives as acetylcholinesterase inhibitors. Bioorg. Med. Chem. (2013);21(17):4928-37. https://doi.org/10.1016/j.bmc.2013.06.065
- Surve P, Ravindran S, Acharjee A, Rastogi H, Basu S, Honrao P. Metabolite characterization of anti-cancer agent Gefitinib in human hepatocytes. Drug Metab Lett. (2013);7:126-136. https://doi.org/10.2174/1872312808666140317154110
- Akalın Çiftçi G, Temel HE, Yurttaş L. Apoptotic Effect of Novel Benzimidazole Derivatives Bearing Pyridyl/Pyrimidinyl Piperazine Moiety. Anti-Cancer Agents Med. Chem., (2022);22:1780-1792. https://doi.org/10.2174/1871520621666210708095110
- Ellman G.L., Courtney K.D., Anders V., Featherstone R.M. A New And Rapid Colorimetric Determination Of Acetylcholinesterase Activity. Biochem. Pharmacol. (1961);7:88-95. https://doi.org/10.1016/0006-2952(61)90145-9
- Mosmann T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J Immunol Methods. (1983);65,(1-2):55-63. https://doi.org/10.1016/0022-1759(83)90303-4
- Keiser K., Johnson C.C., Tipton D.A. Cytotoxicity of mineral trioxide aggregate using human periodontal ligament fibroblasts. Journal of Endodontics. (2000); 26: 288-291. https://doi.org/10.1097/00004770-200005000-00010
- Yurttaş L, Ozkay Y, Demirci F, Göger G, Ulusoylar-Yıldırım Ş, Abu Mohsen U, Öztürk Ö, Kaplancıklı ZA. Synthesis, anticandidal activity, and cytotoxicity of some thiazole derivatives with dithiocarbamate side chains, Turk J Chem. (2014);38:815-824. https://doi.org/10.3906/kim-1312-62
- Ji F, Fengqi B, MinGu, Jing L, Zhipeng Z, Jiaoli D, Sai-Sai X and Jinsong D. Design, synthesis and evaluation of quinolinone derivatives containing dithiocarbamate moiety as multifunctional AChE inhibitors for the treatmentof Alzheimer’s disease, J Enzyme Inhib Med Chem. (2020);35:118-128. https://doi.org/10.1080/14756366.2019.1687460
- Honghua Z, Yuying W, Yuqing W, Xuelin L, Şuji W, Zhen W. Recent advance on carbamate-based cholinesterase inhibitors as potential multifunctional agents against Alzheimer’s disease, Eur J Med Chem. (2022); 240:114606. https://doi.org/10.1016/j.ejmech.2022.114606
Toplam 24 adet kaynakça vardır.
Ayrıntılar
| Birincil Dil | İngilizce |
|---|---|
| Konular | Toksikoloji |
| Bölüm | Research Articles |
| Yazarlar | |
| Proje Numarası | 1404S116 |
| Yayımlanma Tarihi | 28 Ağustos 2023 |
| Gönderilme Tarihi | 17 Temmuz 2023 |
| Yayımlandığı Sayı | Yıl 2023 Cilt: 2 Sayı: 2 |
