메뉴 건너뛰기




Volumn 120, Issue 6, 2013, Pages 883-891

Synthesis, molecular modeling, and in vitro screening of monoamine oxidase inhibitory activities of some novel hydrazone derivatives

Author keywords

5 methyl 2 benzoxazolinone; Human monoamine oxidase B inhibitors; Hydrazone; Molecular docking

Indexed keywords

2 [2 (5 METHYL 2 BENZOXAZOLINONE 3 YL)ACETYL] 3/4/5 SUBSTITUTED BENZYLIDENEHYDRAZINE DERIVATIVE; AMINE OXIDASE (FLAVIN CONTAINING); AMINE OXIDASE (FLAVIN CONTAINING) ISOENZYME A; BENZALDEHYDE DERIVATIVE; HYDRAZONE DERIVATIVE; MONOAMINE OXIDASE B INHIBITOR; SELEGILINE; UNCLASSIFIED DRUG;

EID: 84878699680     PISSN: 03009564     EISSN: 14351463     Source Type: Journal    
DOI: 10.1007/s00702-013-0968-2     Document Type: Article
Times cited : (18)

References (43)
  • 1
    • 0027429999 scopus 로고
    • Monoamine oxidase inhibitors and the cheese effect
    • 8255365 10.1007/BF00978365 1:CAS:528:DyaK2cXitlWjsQ%3D%3D
    • Anderson MC, Hasan F, McCrodden JM, Tipton KF (1993) Monoamine oxidase inhibitors and the cheese effect. Neurochem Res 18:1145-1149
    • (1993) Neurochem Res , vol.18 , pp. 1145-1149
    • Anderson, M.C.1    Hasan, F.2    McCrodden, J.M.3    Tipton, K.F.4
  • 2
    • 36148955400 scopus 로고    scopus 로고
    • Structures of human monoamine oxidase B complexes with selective noncovalent inhibitors: Safinamide and coumarin analogs
    • 17915852 10.1021/jm070677y 1:CAS:528:DC%2BD2sXhtFWgurjI
    • Binda C, Wang J, Pisani L, Caccia C, Carotti A, Salvati P, Edmondson DE, Mattevi A (2007) Structures of human monoamine oxidase B complexes with selective noncovalent inhibitors: safinamide and coumarin analogs. J Med Chem 50:5848-5852
    • (2007) J Med Chem , vol.50 , pp. 5848-5852
    • Binda, C.1    Wang, J.2    Pisani, L.3    Caccia, C.4    Carotti, A.5    Salvati, P.6    Edmondson, D.E.7    Mattevi, A.8
  • 3
    • 0017184389 scopus 로고
    • A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding
    • 942051 10.1016/0003-2697(76)90527-3 1:CAS:528:DyaE28XksVehtrY%3D
    • Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72:248-254
    • (1976) Anal Biochem , vol.72 , pp. 248-254
    • Bradford, M.M.1
  • 4
    • 33847420851 scopus 로고    scopus 로고
    • Selective inhibitory activity against MAO and molecular modeling studies of 2-thiazolylhydrazone derivatives
    • 17253676 10.1021/jm060869d 1:CAS:528:DC%2BD2sXot1ansg%3D%3D
    • Chimenti F, Maccioni E, Secci D, Bolasco A, Chimenti P et al (2007) Selective inhibitory activity against MAO and molecular modeling studies of 2-thiazolylhydrazone derivatives. J Med Chem 50:707-712
    • (2007) J Med Chem , vol.50 , pp. 707-712
    • Chimenti, F.1    Maccioni, E.2    Secci, D.3    Bolasco, A.4    Chimenti, P.5
  • 5
    • 50249143998 scopus 로고    scopus 로고
    • Synthesis, stereochemical identification, and selective inhibitory activity against human monoamine oxidase-B of 2-methylcyclohexylidene-(4- arylthiazol-2-yl)hydrazones
    • 18666768 10.1021/jm800132g 1:CAS:528:DC%2BD1cXpt1ygtb8%3D
    • Chimenti F, Maccioni E, Secci D, Bolasco A, Chimenti P et al (2008) Synthesis, stereochemical identification, and selective inhibitory activity against human monoamine oxidase-B of 2-methylcyclohexylidene-(4-arylthiazol-2- yl)hydrazones. J Med Chem 51:4874-4880
    • (2008) J Med Chem , vol.51 , pp. 4874-4880
    • Chimenti, F.1    Maccioni, E.2    Secci, D.3    Bolasco, A.4    Chimenti, P.5
  • 6
    • 77956325073 scopus 로고    scopus 로고
    • Synthesis and selective inhibition of human monoamine oxidases of a large scaffold of (4,5-substituted-thiazol-2-yl)hydrazones
    • 10.1039/c0md00014k 1:CAS:528:DC%2BC3cXhtVeju7vI
    • Chimenti F, Secci D, Bolasco A, Chimenti P, Arianna Granese A, Carradori S, D'Ascenzio M et al (2010a) Synthesis and selective inhibition of human monoamine oxidases of a large scaffold of (4,5-substituted-thiazol-2-yl) hydrazones. Med Chem Commun 1:61-72
    • (2010) Med Chem Commun , vol.1 , pp. 61-72
    • Chimenti, F.1    Secci, D.2    Bolasco, A.3    Chimenti, P.4    Arianna Granese, A.5    Carradori, S.6    D'Ascenzio, M.7
  • 7
    • 77955325332 scopus 로고    scopus 로고
    • Synthesis, semipreparative HPLC separation, biological evaluation, and 3D-QSAR of hydrazothiazole derivatives as human monoamine oxidase B inhibitors
    • 20579890 10.1016/j.bmc.2010.05.070 1:CAS:528:DC%2BC3cXoslagtbs%3D
    • Chimenti F, Secci D, Bolasco A, Chimenti P, Arianna Granese A, Carradori S, Maccioni E et al (2010b) Synthesis, semipreparative HPLC separation, biological evaluation, and 3D-QSAR of hydrazothiazole derivatives as human monoamine oxidase B inhibitors. Bioorg Med Chem 18:5063-5070
    • (2010) Bioorg Med Chem , vol.18 , pp. 5063-5070
    • Chimenti, F.1    Secci, D.2    Bolasco, A.3    Chimenti, P.4    Arianna Granese, A.5    Carradori, S.6    Maccioni, E.7
  • 8
    • 73549097080 scopus 로고    scopus 로고
    • Synthesis and inhibitory activity against human monoamine oxidase of N1-thiocarbamoyl-3,5-di(hetero)aryl-4,5-dihydro-(1H)-pyrazole derivatives
    • 19926363 10.1016/j.ejmech.2009.11.003 1:CAS:528:DC%2BC3cXos1Smtg%3D%3D
    • Chimenti F, Carradori S, Secci D, Bolasco A, Bizzarri B et al (2010c) Synthesis and inhibitory activity against human monoamine oxidase of N1-thiocarbamoyl-3,5-di(hetero)aryl-4,5-dihydro-(1H)-pyrazole derivatives. Eur J Med Chem 45:800-804
    • (2010) Eur J Med Chem , vol.45 , pp. 800-804
    • Chimenti, F.1    Carradori, S.2    Secci, D.3    Bolasco, A.4    Bizzarri, B.5
  • 9
    • 33947437988 scopus 로고
    • The analgesic activity of some benzoxazolone derivatives
    • 18128352 10.1021/ja01172a036 1:CAS:528:DyaH1MXjs1GksQ%3D%3D
    • Close WJ, Tiffany BD, Spielman MA (1949) The analgesic activity of some benzoxazolone derivatives. J Am Chem Soc 71:1265-1268
    • (1949) J Am Chem Soc , vol.71 , pp. 1265-1268
    • Close, W.J.1    Tiffany, B.D.2    Spielman, M.A.3
  • 10
    • 84855994429 scopus 로고    scopus 로고
    • Synthesis and biological assessment of novel 2-thiazolylhydrazones and computational analysis of their recognition by monoamine oxidase
    • Distinto S, Yanez M, Alcaro S, M. Cardia C, Gaspari M et al. (2012) Synthesis and biological assessment of novel 2-thiazolylhydrazones and computational analysis of their recognition by monoamine oxidase B. Eur J Med Chem 48:284-295
    • (2012) B. Eur J Med Chem , vol.48 , pp. 284-295
    • Distinto, S.1    Yanez, M.2    Alcaro, S.3    Cardia, C.M.4    Gaspari, M.5
  • 11
    • 56749085833 scopus 로고    scopus 로고
    • The increasing role of monoamine oxidase type B inhibitors in Parkinson's disease therapy
    • 18937611 10.1517/14656566.9.16.2759 1:CAS:528:DC%2BD1cXht1Ont7bK
    • Elmer LW, Bertoni JM (2008) The increasing role of monoamine oxidase type B inhibitors in Parkinson's disease therapy. Expert Opin Pharmacother 9:2759-2772
    • (2008) Expert Opin Pharmacother , vol.9 , pp. 2759-2772
    • Elmer, L.W.1    Bertoni, J.M.2
  • 12
    • 34447280369 scopus 로고    scopus 로고
    • A new therapeutic approach in alzheimer disease: Some novel pyrazole derivatives as dual MAO-B inhibitors and antiinflammatory analgesics
    • 17611112 10.1016/j.bmc.2007.06.004
    • Gökhan-Kelekçi N, Yabanoǧlu S, Küpeli E, SalgIn U, Özgen Ö et al (2007) A new therapeutic approach in alzheimer disease: some novel pyrazole derivatives as dual MAO-B inhibitors and antiinflammatory analgesics. Bioorg Med Chem 15:5775-5786
    • (2007) Bioorg Med Chem , vol.15 , pp. 5775-5786
    • Gökhan-Kelekçi, N.1    Yabanoǧlu, S.2    Küpeli, E.3    Salgin, U.4    Özgen, O.5
  • 13
    • 58549107997 scopus 로고    scopus 로고
    • New pyrazoline bearing 4(3H)-quinazolinone inhibitors of monoamine oxidase: Synthesis, biological evaluation, and structural determinants of MAO-A and MAO-B selectivity
    • 19091581 10.1016/j.bmc.2008.11.068
    • Gökhan-Kelekçi N, Koyunoǧlu S, Yabanoǧlu S, Yelekçi K, Özgen Ö et al (2009a) New pyrazoline bearing 4(3H)-quinazolinone inhibitors of monoamine oxidase: synthesis, biological evaluation, and structural determinants of MAO-A and MAO-B selectivity. Bioorg Med Chem 17:675-689
    • (2009) Bioorg Med Chem , vol.17 , pp. 675-689
    • Gökhan-Kelekçi, N.1    Koyunoǧlu, S.2    Yabanoǧlu, S.3    Yelekçi, K.4    Özgen, O.5
  • 14
    • 69249111386 scopus 로고    scopus 로고
    • Synthesis and molecular modeling of some novel hexahydroindazole derivatives as potent monoamine oxidase inhibitors
    • 19682910 10.1016/j.bmc.2009.07.033
    • Gökhan-Kelekçi N, Şimşek ÖÖ, Ercan A, Yelekçi K, Şahin ZS et al (2009b) Synthesis and molecular modeling of some novel hexahydroindazole derivatives as potent monoamine oxidase inhibitors. Bioorg Med Chem 17:6761-6772
    • (2009) Bioorg Med Chem , vol.17 , pp. 6761-6772
    • Gökhan-Kelekçi, N.1    Şimşek, O.2    Ercan, A.3    Yelekçi, K.4    Şahin, Z.S.5
  • 15
    • 80054978038 scopus 로고    scopus 로고
    • Synthesis and in vitro cytotoxic activity of novel pyrazolo[3,4-d] pyrimidines and related pyrazole hydrazones toward breast adenocarcinoma MCF-7 cell line
    • Hassan GS, Kadry HH, Abou-Seri SM, Ali MM, El-Din Mahmoud AE (2011) Synthesis and in vitro cytotoxic activity of novel pyrazolo[3,4-d]pyrimidines and related pyrazole hydrazones toward breast adenocarcinoma MCF-7 cell line. Bioorg Med Chem 19:6808-6817
    • (2011) Bioorg Med Chem , vol.19 , pp. 6808-6817
    • Hassan, G.S.1    Kadry, H.H.2    Abou-Seri, S.M.3    Ali, M.M.4    El-Din Mahmoud, A.E.5
  • 16
    • 33646824066 scopus 로고
    • NMR-spektroskopische Untersuchungen an Derivaten des 2,4- Dichlorphenoxyessigsäurehydrazids
    • 10.1007/BF00814150 1:CAS:528:DyaK2cXisVelu7k%3D
    • Himmelreich U, Tschwatschal F, Borsdorf R (1993) NMR-spektroskopische Untersuchungen an Derivaten des 2,4-Dichlorphenoxyessigsäurehydrazids. Monatsh Chem 124:1041-1051
    • (1993) Monatsh Chem , vol.124 , pp. 1041-1051
    • Himmelreich, U.1    Tschwatschal, F.2    Borsdorf, R.3
  • 17
    • 33947716119 scopus 로고    scopus 로고
    • A semi-empirical free energy force field with charge-based desolvation
    • 10.1002/jcc.20634 1:CAS:528:DC%2BD2sXjsVSms78%3D
    • Huey R, Morris GM, Olson AJ, Goodsell DS (2007) A semi-empirical free energy force field with charge-based desolvation. J Comp Chem 28:1145-1152
    • (2007) J Comp Chem , vol.28 , pp. 1145-1152
    • Huey, R.1    Morris, G.M.2    Olson, A.J.3    Goodsell, D.S.4
  • 18
    • 57349123793 scopus 로고    scopus 로고
    • Imidazole derivatives. XXX. Synthesis and antitumor activity of 4-amyloxy-3-nitroacetophenone 2-imidazolinyl-2-hydrazone and related compounds
    • 10.1007/s11094-008-0133-7 1:CAS:528:DC%2BD1cXhsVaisbjM
    • Iradyan MA, Aroyan RA, Stepanyan GM, Arsenyan FG, Garibdzhanyan BT (2008) Imidazole derivatives. XXX. Synthesis and antitumor activity of 4-amyloxy-3-nitroacetophenone 2-imidazolinyl-2-hydrazone and related compounds. Pharm Chem J 42:384-386
    • (2008) Pharm Chem J , vol.42 , pp. 384-386
    • Iradyan, M.A.1    Aroyan, R.A.2    Stepanyan, G.M.3    Arsenyan, F.G.4    Garibdzhanyan, B.T.5
  • 19
    • 33751032349 scopus 로고    scopus 로고
    • Synthesis and characterization of novel hydrazide-hydrazones and the study of their structure-antituberculosis activity
    • 10.1016/j.ejmech.2006.06.009
    • Koçyiǧit-KaymakçIoǧlu B, Oruç E, Unsalan S, Kandemirli F, Shvets N et al (2006) Synthesis and characterization of novel hydrazide-hydrazones and the study of their structure-antituberculosis activity. Eur J Med Chem 41:1253-1261
    • (2006) Eur J Med Chem , vol.41 , pp. 1253-1261
    • Koçyiǧit-Kaymakçioǧlu, B.1    Oruç, E.2    Unsalan, S.3    Kandemirli, F.4    Shvets, N.5
  • 20
    • 0344875120 scopus 로고    scopus 로고
    • Synthesis and biological activities of diflunisal hydrazide-/hydrazones
    • 14642333 10.1016/j.ejmech.2003.08.004
    • Küçükgüzel SG, Mazi A, Sahin F, Öztürk S, Stables J (2003) Synthesis and biological activities of diflunisal hydrazide-/hydrazones. Eur J Med Chem 38:1005-1013
    • (2003) Eur J Med Chem , vol.38 , pp. 1005-1013
    • Küçükgüzel, S.G.1    Mazi, A.2    Sahin, F.3    Öztürk, S.4    Stables, J.5
  • 21
    • 67650395645 scopus 로고    scopus 로고
    • Synthesis and anticonvulsant activity of some new bishydrazones derived from 3,4-dipropyloxythiophene
    • 19286282 10.1016/j.ejmech.2009.02.009 1:CAS:528:DC%2BD1MXoslGhs7w%3D
    • Kulandasamy R, Adhikari AV, Stables JP (2009a) Synthesis and anticonvulsant activity of some new bishydrazones derived from 3,4-dipropyloxythiophene. Eur J Med Chem 44:3672-3679
    • (2009) Eur J Med Chem , vol.44 , pp. 3672-3679
    • Kulandasamy, R.1    Adhikari, A.V.2    Stables, J.P.3
  • 22
    • 70349764478 scopus 로고    scopus 로고
    • A new class of anticonvulsants possessing 6 Hz activity: 3,4-dialkyloxy thiophene bishydrazones
    • 19556038 10.1016/j.ejmech.2009.05.026 1:CAS:528:DC%2BD1MXht1GgtbzL
    • Kulandasamy R, Adhikari AV, Stables JP (2009b) A new class of anticonvulsants possessing 6 Hz activity: 3,4-dialkyloxy thiophene bishydrazones. Eur J Med Chem 44:4376-4384
    • (2009) Eur J Med Chem , vol.44 , pp. 4376-4384
    • Kulandasamy, R.1    Adhikari, A.V.2    Stables, J.P.3
  • 23
    • 0344443765 scopus 로고    scopus 로고
    • Oxidative a-ketoglutarate dehydrogenase inhibition via subtle elevations in monoamine oxidase B levels results in loss of spare respiratory capacity: Implication for Parkinson's disease
    • 12963742 10.1074/jbc.M306378200 1:CAS:528:DC%2BD3sXovFKltbY%3D
    • Kumar MJ, Nicholls DG, Andersen JK (2003) Oxidative a-ketoglutarate dehydrogenase inhibition via subtle elevations in monoamine oxidase B levels results in loss of spare respiratory capacity: implication for Parkinson's disease. J Biol Chem 278:46432-46439
    • (2003) J Biol Chem , vol.278 , pp. 46432-46439
    • Kumar, M.J.1    Nicholls, D.G.2    Andersen, J.K.3
  • 24
    • 50349086297 scopus 로고    scopus 로고
    • N-Propynyl analogs of b-phenylethylidenehydrazines: Synthesis and evaluation of effects on glycine, GABA, and monoamine oxidase
    • 18693021 10.1016/j.bmc.2008.07.027 1:CAS:528:DC%2BD1cXhtVyktbfL
    • MacKenzie EM, Fassihi A, Davood A, Chen O-H, Rauw G, Rauw G, Knaus EE, Baker GB (2008) N-Propynyl analogs of b-phenylethylidenehydrazines: synthesis and evaluation of effects on glycine, GABA, and monoamine oxidase. Bioorg Med Chem 16:8254-8263
    • (2008) Bioorg Med Chem , vol.16 , pp. 8254-8263
    • Mackenzie, E.M.1    Fassihi, A.2    Davood, A.3    Chen, O.-H.4    Rauw, G.5    Rauw, G.6    Knaus, E.E.7    Baker, G.B.8
  • 25
    • 0006297269 scopus 로고    scopus 로고
    • Synthesis of 1-(2-hydroxyphenyl)-2,4-imidazolidinedione derivatives through cyclic transformations of ethyl 2-oxo-3(2H)-benzoxazoleacetate derivatives
    • 10.1002/jhet.5570330645 1:CAS:528:DyaK2sXotFCkug%3D%3D
    • Milcent R, Akhnazarian A, Lensen N (1996) Synthesis of 1-(2-hydroxyphenyl)-2,4-imidazolidinedione derivatives through cyclic transformations of ethyl 2-oxo-3(2H)-benzoxazoleacetate derivatives. J Heterocycl Chem 33:1829-1833
    • (1996) J Heterocycl Chem , vol.33 , pp. 1829-1833
    • Milcent, R.1    Akhnazarian, A.2    Lensen, N.3
  • 26
    • 79251515011 scopus 로고    scopus 로고
    • Novel synthesis of hydrazide-hydrazone derivatives and their utilization in the synthesis of coumarin, pyridine, thiazole and thiophene derivatives with antitumor activity
    • 10.3390/molecules16010016 1:CAS:528:DC%2BC3MXjtlWrtA%3D%3D
    • Mohareb RM, Fleita DH, Sakka OK (2011) Novel synthesis of hydrazide-hydrazone derivatives and their utilization in the synthesis of coumarin, pyridine, thiazole and thiophene derivatives with antitumor activity. Molecules 16:16-27
    • (2011) Molecules , vol.16 , pp. 16-27
    • Mohareb, R.M.1    Fleita, D.H.2    Sakka, O.K.3
  • 27
    • 79151483364 scopus 로고    scopus 로고
    • Synthesis and anti-inflammatory evaluation of some new acyl-hydrazones bearing 2-aryl-thiazole
    • 21163557 10.1016/j.ejmech.2010.11.032 1:CAS:528:DC%2BC3MXpvVaisQ%3D%3D
    • Moldovan CM, Oniga O, Parvu A, Tiperciuc B, Verite P et al (2011) Synthesis and anti-inflammatory evaluation of some new acyl-hydrazones bearing 2-aryl-thiazole. Eur J Med Chem 46:526-534
    • (2011) Eur J Med Chem , vol.46 , pp. 526-534
    • Moldovan, C.M.1    Oniga, O.2    Parvu, A.3    Tiperciuc, B.4    Verite, P.5
  • 29
    • 79959947636 scopus 로고    scopus 로고
    • Synthesis and antidepressant-like activity evaluation of sulphonamides and sulphonyl-hydrazones
    • 21696965 10.1016/j.bmc.2011.05.056
    • Oliveira KN, Costa P, Santin JR, Mazzambani L, Bürger C et al (2011) Synthesis and antidepressant-like activity evaluation of sulphonamides and sulphonyl-hydrazones. Bioorg Med Chem 19:4295-4306
    • (2011) Bioorg Med Chem , vol.19 , pp. 4295-4306
    • Oliveira, K.N.1    Costa, P.2    Santin, J.R.3    Mazzambani, L.4    Bürger, C.5
  • 30
    • 0000544558 scopus 로고
    • Conformational behaviour and E/Z isomerization of N-acyl and N-aroylhydrazones
    • 10.1016/S0040-4020(01)87332-4 1:CAS:528:DyaL2sXhsFGls7k%3D
    • Palla G, Predieri G, Domiano P (1986) Conformational behaviour and E/Z isomerization of N-acyl and N-aroylhydrazones. Tetrahedron 42:3649-3654
    • (1986) Tetrahedron , vol.42 , pp. 3649-3654
    • Palla, G.1    Predieri, G.2    Domiano, P.3
  • 31
    • 77950860543 scopus 로고    scopus 로고
    • Synthesis and antimicrobial activity of cholic acid hydrazone analogues
    • 20181416 10.1016/j.ejmech.2010.02.006 1:CAS:528:DC%2BC3cXkvFeisL8%3D
    • Rasras AJM, Al-Tel TH, Al-Aboudi AF, Al-Qawasmeh RA (2010) Synthesis and antimicrobial activity of cholic acid hydrazone analogues. Eur J Med Chem 45:2307-2313
    • (2010) Eur J Med Chem , vol.45 , pp. 2307-2313
    • Rasras, A.J.M.1    Al-Tel, T.H.2    Al-Aboudi, A.F.3    Al-Qawasmeh, R.A.4
  • 32
    • 34548385246 scopus 로고    scopus 로고
    • Biological activities of hydrazone derivatives
    • 17960096 10.3390/12081910 1:CAS:528:DC%2BD2sXhtFGntLvF
    • Rollas S, Küçükgüzel ŞG (2007) Biological activities of hydrazone derivatives. Molecules 12:1910-1939
    • (2007) Molecules , vol.12 , pp. 1910-1939
    • Rollas, S.1    Küçükgüzel, Ş.2
  • 33
    • 34447267965 scopus 로고    scopus 로고
    • 1-Acylthiosemicarbazides, 1,2,4-triazole-5(4H)-thiones, 1,3,4-thiadiazoles and hydrazones containing 5-methyl-2-benzoxazolinones: Synthesis, analgesic-anti-inflammatory and antimicrobial activities
    • 17587585 10.1016/j.bmc.2007.06.006
    • SalgIn-Gökşen U, Gökhan-Kelekçi N, Göktaş Ö, Köysal Y, KIlIç E et al (2007) 1-Acylthiosemicarbazides, 1,2,4-triazole-5(4H)-thiones, 1,3,4-thiadiazoles and hydrazones containing 5-methyl-2-benzoxazolinones: synthesis, analgesic-anti-inflammatory and antimicrobial activities. Bioorg Med Chem 15:5738-5751
    • (2007) Bioorg Med Chem , vol.15 , pp. 5738-5751
    • Salgin-Gökşen, U.1    Gökhan-Kelekçi, N.2    Göktaş, Ö.3    Köysal, Y.4    Kiliç, E.5
  • 34
    • 0028145566 scopus 로고
    • Increased monoamine oxidase B activity in plaque associated astrocytes of Alzheimer brains revealed by quantitative enzyme radioautography
    • 7816197 10.1016/0306-4522(94)90311-5 1:STN:280:DyaK2M7hsFylug%3D%3D
    • Saura J, Luque JM, Cesura AM, Da Prada M, Chan-Palay V, Huber G, Loffler J, Richards JG (1994) Increased monoamine oxidase B activity in plaque associated astrocytes of Alzheimer brains revealed by quantitative enzyme radioautography. Neuroscience 62:15-30
    • (1994) Neuroscience , vol.62 , pp. 15-30
    • Saura, J.1    Luque, J.M.2    Cesura, A.M.3    Da Prada, M.4    Chan-Palay, V.5    Huber, G.6    Loffler, J.7    Richards, J.G.8
  • 35
    • 44449117421 scopus 로고    scopus 로고
    • Structure of human monoamine oxidase A at 2.2-Å resolution: The control of opening the entry for substrates/inhibitors
    • 18391214 10.1073/pnas.0710626105 1:CAS:528:DC%2BD1cXltFShsLo%3D
    • Son S-Y, Ma J, Kondou Y, Yoshimura M, Yamashita E, Tsukihara T (2008) Structure of human monoamine oxidase A at 2.2-Å resolution: the control of opening the entry for substrates/inhibitors. Proc Natl Acad Sci USA 105:5739-5744
    • (2008) Proc Natl Acad Sci USA , vol.105 , pp. 5739-5744
    • Son, S.-Y.1    Ma, J.2    Kondou, Y.3    Yoshimura, M.4    Yamashita, E.5    Tsukihara, T.6
  • 36
    • 33646567168 scopus 로고    scopus 로고
    • Synthesis, anti-inflammatory and analgesic activity evaluation of some amidine and hydrazone derivatives
    • 16504522 10.1016/j.bmc.2006.02.014 1:CAS:528:DC%2BD28XltVGqtbo%3D
    • Sondhi SM, Dinodia M, Kumar A (2006) Synthesis, anti-inflammatory and analgesic activity evaluation of some amidine and hydrazone derivatives. Bioorg Med Chem 14:4657-4663
    • (2006) Bioorg Med Chem , vol.14 , pp. 4657-4663
    • Sondhi, S.M.1    Dinodia, M.2    Kumar, A.3
  • 39
    • 0037046859 scopus 로고    scopus 로고
    • Hydrazones of 1,2-benzisothiazole hydrazides: Synthesis, antimicrobial activity and QSAR investigations
    • 12126774 10.1016/S0223-5234(02)01378-8 1:CAS:528:DC%2BD38Xltlams7o%3D
    • Vicini P, Zani F, Cozzini P, Doytchinova I (2002) Hydrazones of 1,2-benzisothiazole hydrazides: synthesis, antimicrobial activity and QSAR investigations. Eur J Med Chem 37:553-564
    • (2002) Eur J Med Chem , vol.37 , pp. 553-564
    • Vicini, P.1    Zani, F.2    Cozzini, P.3    Doytchinova, I.4
  • 40
    • 0040812931 scopus 로고    scopus 로고
    • N-(E)-2-stilbenyloxymethylenecarbonyl substituted hydrazones of ortho, meta and para hydroxybenzaldehydes
    • Wyrzykiewicz E, Blaszczyk A, Turowska-Tyrk I (2000) N-(E)-2- stilbenyloxymethylenecarbonyl substituted hydrazones of ortho, meta and para hydroxybenzaldehydes. Bull Pol Acad Sci Chem 4:213-229
    • (2000) Bull Pol Acad Sci Chem , vol.4 , pp. 213-229
    • Wyrzykiewicz, E.1    Blaszczyk, A.2    Turowska-Tyrk, I.3
  • 41
    • 33646092535 scopus 로고    scopus 로고
    • Inhibitory effects of cis- and trans-resveratrol on noradrenaline and 5-hydroxytryptamine uptake and on monoamine oxidase activity
    • 16631124 10.1016/j.bbrc.2006.03.190
    • Yáñez M, Fraiz N, Cano E, Orallo F (2006) Inhibitory effects of cis- and trans-resveratrol on noradrenaline and 5-hydroxytryptamine uptake and on monoamine oxidase activity. Biochem Biophys Res Commun 344:688-695
    • (2006) Biochem Biophys Res Commun , vol.344 , pp. 688-695
    • Yáñez, M.1    Fraiz, N.2    Cano, E.3    Orallo, F.4
  • 42
    • 34250792398 scopus 로고    scopus 로고
    • Docking of novel reversible monoamine oxidase-B inhibitors: Efficient prediction of ligand binding sites and estimation of inhibitors thermodynamic properties
    • 17401533 10.1007/s00702-007-0679-7
    • Yelekçi K, Karahan Ö, ToprakçI M (2007) Docking of novel reversible monoamine oxidase-B inhibitors: efficient prediction of ligand binding sites and estimation of inhibitors thermodynamic properties. J Neural Transm 114:725-732
    • (2007) J Neural Transm , vol.114 , pp. 725-732
    • Yelekçi, K.1    Karahan, Ö.2    Toprakçi, M.3
  • 43
    • 33645307953 scopus 로고    scopus 로고
    • The therapeutic potential of monoamine oxidase inhibitors
    • 16552415 10.1038/nrn1883 1:CAS:528:DC%2BD28Xis1Gksrs%3D
    • Youdim MBH, Edmondson D, Tipton KF (2006) The therapeutic potential of monoamine oxidase inhibitors. Nat Rev Neurosci 7:295-309
    • (2006) Nat Rev Neurosci , vol.7 , pp. 295-309
    • Youdim, M.B.H.1    Edmondson, D.2    Tipton, K.F.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.