메뉴 건너뛰기




Volumn 52, Issue 12, 2002, Pages 863-869

Synthesis and evaluation of anticonvulsant activities of some bis Mannich bases and corresponding piperidinols

Author keywords

Acetophenones, anticonvulsant activity, bis Mannich bases, synthesis; Anticonvulsant drugs; Piperidinols

Indexed keywords

1 METHYL 3 BENZOYL 4 HYDROXY 4 PHENYLPIPERIDINE; 1 METHYL [3 (4 CHLOROBENZOYL)][4 HYDROXY 4 (4 CHLOROPHENYL)]PIPERIDINE; 3,3' METHYLIMINOBIS(1 PHENYL 1 PROPANONE); 3,3' METHYLIMINOBIS[1 (4 CHLOROPHENYL 1 PROPANONE)]; 3,3' METHYLIMINOBIS[1 (4 METHOXYPHENYL 1 PROPANONE)]; 3,3' METHYLIMINOBIS[1 (4 METHYLPHENYL 1 PROPANONE)]; ACETOPHENONE DERIVATIVE; MANNICH BASE; PENTETRAZOLE; PIPERIDINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0036918544     PISSN: 00044172     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0031-1299982     Document Type: Article
Times cited : (36)

References (33)
  • 1
    • 0018129707 scopus 로고
    • Antiepileptic drug development: II. Anticonvulsant drug screening
    • Krall, R. L., Penry, J. K., White, B. G. et al., Antiepileptic drug development: II. Anticonvulsant drug screening. Epilepsia 9, 409 (1978)
    • (1978) Epilepsia , vol.9 , pp. 409
    • Krall, R.L.1    Penry, J.K.2    White, B.G.3
  • 5
    • 0028318455 scopus 로고
    • Antimicrobial evaluation of some styryl ketone derivatives and related thiol adducts
    • Erciyas, E., Erkaleli, H. I., Cosar, G., Antimicrobial evaluation of some styryl ketone derivatives and related thiol adducts. J. Pharm. Sci. 83, 545 (1994)
    • (1994) J. Pharm. Sci. , vol.83 , pp. 545
    • Erciyas, E.1    Erkaleli, H.I.2    Cosar, G.3
  • 6
    • 0036407185 scopus 로고    scopus 로고
    • Antimicrobial evaluation of some Mannich bases of acetophenones and representative quaternary derivatives
    • Gul, H. I., Denizci, A. A., Erciyas, E., Antimicrobial evaluation of some Mannich bases of acetophenones and representative quaternary derivatives. Arzneim.-Forsch./Drug Res. 52, 773 (2002)
    • (2002) Arzneim.-Forsch./Drug Res. , vol.52 , pp. 773
    • Gul, H.I.1    Denizci, A.A.2    Erciyas, E.3
  • 7
    • 0035133288 scopus 로고    scopus 로고
    • Antifungal activity of some mono, bis and quaternary Mannich bases derived from acetophenone
    • Gul, H. I., Ojanen, T., Vepsalainen, J. et al., Antifungal activity of some mono, bis and quaternary Mannich bases derived from acetophenone. Arzneim.-Forsch./Drug Res. 51 (I), 72 (2001)
    • (2001) Arzneim.-Forsch./Drug Res. , vol.51 , Issue.1 , pp. 72
    • Gul, H.I.1    Ojanen, T.2    Vepsalainen, J.3
  • 8
    • 0033995992 scopus 로고    scopus 로고
    • Cytotoxic activities of mono and bis Mannich bases derived from acetophenone against Renca and Jurkat cells
    • Gul, H. I., Vepsalainen, J., Gul, M. et al., Cytotoxic activities of mono and bis Mannich bases derived from acetophenone against Renca and Jurkat cells. Pharm. Acta Helv. 74, 393 (2000)
    • (2000) Pharm. Acta Helv. , vol.74 , pp. 393
    • Gul, H.I.1    Vepsalainen, J.2    Gul, M.3
  • 9
    • 0036350482 scopus 로고    scopus 로고
    • Syntheses and stability studies of some Mannich bases of acetophenones and evaluation of their cytotoxicity against Jurkat cells
    • Gul, H. I., Gul, M., Erciyas, E., Syntheses and stability studies of some Mannich bases of acetophenones and evaluation of their cytotoxicity against Jurkat cells. Arzneim.-Forsch./Drug Res. 52, 628 (2002)
    • (2002) Arzneim.-Forsch./Drug Res. , vol.52 , pp. 628
    • Gul, H.I.1    Gul, M.2    Erciyas, E.3
  • 10
    • 0017855453 scopus 로고
    • Diuretic activity of Mannich base derivatives of ethacrynic acid and certain ethacrynic acid analogues
    • Koechel, D. A., Rankin, G. O., Diuretic activity of Mannich base derivatives of ethacrynic acid and certain ethacrynic acid analogues. J. Med. Chem. 21, 764 (1978)
    • (1978) J. Med. Chem. , vol.21 , pp. 764
    • Koechel, D.A.1    Rankin, G.O.2
  • 11
    • 0017742877 scopus 로고
    • 1,3-Dicyclohexyl-5-alkyl-5-aminome-thylbarbituric acids as potential antiinflammatory agents
    • Sladowska, H., 1,3-Dicyclohexyl-5-alkyl-5-aminome-thylbarbituric acids as potential antiinflammatory agents. Farmaco. Sci. 32, 866 (1977)
    • (1977) Farmaco. Sci. , vol.32 , pp. 866
    • Sladowska, H.1
  • 12
    • 0023887856 scopus 로고
    • The in vitro and in vivo antimalarial activity of some Mannich bases derived from 4-[7′-bromo (and chloro)- 1′,5′-naphthyridin-4′-ylamino]-phenol and 4-(7′-trifluoromethylquinolin-4′-ylamino)phenol
    • Scott, H. V., Tan, W. L., Barlin, G. B., The in vitro and in vivo antimalarial activity of some Mannich bases derived from 4-[7′-bromo (and chloro)- 1′,5′-naphthyridin-4′-ylamino]-phenol and 4-(7′-trifluoromethylquinolin-4′-ylamino)phenol. Ann. Trop. Med. Parasitol. 82, 127 (1988)
    • (1988) Ann. Trop. Med. Parasitol. , vol.82 , pp. 127
    • Scott, H.V.1    Tan, W.L.2    Barlin, G.B.3
  • 13
    • 0030969247 scopus 로고    scopus 로고
    • New quinoline di-Mannich base compounds with greater antimalarial activity than chloroquine, amodiaquine, or pyronaridine
    • Kotecka, B. M., Barlin, G. B., Edstein, M. D. et al., New quinoline di-Mannich base compounds with greater antimalarial activity than chloroquine, amodiaquine, or pyronaridine. Antimicrob. Agents. Chemother. 41, 1369 (1997)
    • (1997) Antimicrob. Agents. Chemother. , vol.41 , pp. 1369
    • Kotecka, B.M.1    Barlin, G.B.2    Edstein, M.D.3
  • 14
    • 0026672298 scopus 로고
    • The in vitro and in vivo antimalarial activity of some Mannich bases derived from 4-(7′-trifluoromethyl-1′,5′-naphthyridin-4′-ylamino) phenol, 2-(7′-trifluoromethyl-quinolin-4′-ylamino)phenol, and 4′-chloro-5-(7"-trifluoromethylquinolin-4"-ylamino)bi- phenyl-2-ols
    • Barlin, G. B., Jiravinyu, C., Butcher, G. A. et al., The in vitro and in vivo antimalarial activity of some Mannich bases derived from 4-(7′-trifluoromethyl-1′,5′-naphthyridin-4′-ylamino) phenol, 2-(7′-trifluoromethyl-quinolin-4′-ylamino)phenol, and 4′-chloro-5-(7"-trifluoromethylquinolin-4"-ylamino)bi- phenyl-2-ols. Ann. Trop. Med. Parasitol. 86, 323 (1992)
    • (1992) Ann. Trop. Med. Parasitol. , vol.86 , pp. 323
    • Barlin, G.B.1    Jiravinyu, C.2    Butcher, G.A.3
  • 15
    • 0023239159 scopus 로고
    • Anticonvulsant activity of indanylspirosuccinimide Mannich bases
    • Borenstein, M. R., Doukas, P. H., Anticonvulsant activity of indanylspirosuccinimide Mannich bases. J. Pharm. Sci. 76, 300 (1987)
    • (1987) J. Pharm. Sci. , vol.76 , pp. 300
    • Borenstein, M.R.1    Doukas, P.H.2
  • 16
    • 0026799498 scopus 로고
    • Anticonvulsant properties of some Mannich bases of conjugated arylidene ketones
    • Dimmock, J. R., Jonnalagadda, S. S., Phillips, O. A. et al., Anticonvulsant properties of some Mannich bases of conjugated arylidene ketones. J. Pharm. Sci. 81, 436 (1992)
    • (1992) J. Pharm. Sci. , vol.81 , pp. 436
    • Dimmock, J.R.1    Jonnalagadda, S.S.2    Phillips, O.A.3
  • 17
    • 0013830187 scopus 로고
    • Beta-aminoketones as anti-infective agents
    • G. L. Hobby (ed.), American Society for Microbiology, Bethesda, MD
    • Gordon, P. N., Johnston, J. D., English, A. R., Beta-aminoketones as anti-infective agents, in: G. L. Hobby (ed.), Antimicrobial Agents and Chemotherapy, pp. 165, American Society for Microbiology, Bethesda, MD (1965)
    • (1965) Antimicrobial Agents and Chemotherapy , pp. 165
    • Gordon, P.N.1    Johnston, J.D.2    English, A.R.3
  • 18
    • 0027080953 scopus 로고
    • Evaluation of cytotoxicity of some Mannich bases of various aryl and arylidene ketones and their corresponding arylhydrazones
    • Dimmock, J. R., Advikolanu, K. M., Scott, H. E. et al., Evaluation of cytotoxicity of some Mannich bases of various aryl and arylidene ketones and their corresponding arylhydrazones. J. Pharm. Sci. 81, 1147 (1992)
    • (1992) J. Pharm. Sci. , vol.81 , pp. 1147
    • Dimmock, J.R.1    Advikolanu, K.M.2    Scott, H.E.3
  • 19
    • 0029000822 scopus 로고
    • Synthesis and cytotoxic evaluation of Mesna adducts of some 1-aryl-4,4-dimethyl-5-(1-piperidino)-1-penten-3-one hydrochlorides
    • Dimmock, J. R., Kumar, P., Chen, M. et al., Synthesis and cytotoxic evaluation of Mesna adducts of some 1-aryl-4,4-dimethyl-5-(1-piperidino)-1-penten-3-one hydrochlorides. Pharmazie. 50, 449 (1995)
    • (1995) Pharmazie. , vol.50 , pp. 449
    • Dimmock, J.R.1    Kumar, P.2    Chen, M.3
  • 20
    • 0034887801 scopus 로고    scopus 로고
    • Effect of acetophenone derived Mannich bases on cellular glutathione level in Jurkat cells/A possible mechanism of action
    • Gul, M., Gul, H. I., Vepsalainen, J. et al., Effect of acetophenone derived Mannich bases on cellular glutathione level in Jurkat cells/A possible mechanism of action. Arzneim.-Forsch./Drug Res. 51 (II), 679 (2001)
    • (2001) Arzneim.-Forsch./Drug Res. , vol.51 , Issue.2 , pp. 679
    • Gul, M.1    Gul, H.I.2    Vepsalainen, J.3
  • 21
    • 0025875837 scopus 로고
    • Evaluation of some Mannich bases of 1-aryl-1-ethanones and related ketones for anticonvulsant activities
    • Dimmock, J. R., Patil, S. A., Shyam, K., Evaluation of some Mannich bases of 1-aryl-1-ethanones and related ketones for anticonvulsant activities. Pharmazie. 46, 538 (1991)
    • (1991) Pharmazie. , vol.46 , pp. 538
    • Dimmock, J.R.1    Patil, S.A.2    Shyam, K.3
  • 22
    • 0012164601 scopus 로고    scopus 로고
    • Hoffmann La Roche Inc., USA, Process for Preparing N-di(beta benzoyl-ethyl)-lower Alkylamines. Patent No. 2, 489, 668 (1949)
    • Plati, J. T., Wenner, W., Montclair, N. J., Hoffmann La Roche Inc., USA, Process for Preparing N-di(beta benzoyl-ethyl)-lower Alkylamines. Patent No. 2, 489, 668 (1949)
    • Plati, J.T.1    Wenner, W.2    Montclair, N.J.3
  • 23
    • 0000236445 scopus 로고
    • 1,3,4-Trisubstituted piperidine derivatives from Mannich bases
    • Plati, J. T., Schmidt, R. A., Wenner, W., 1,3,4-Trisubstituted piperidine derivatives from Mannich bases. J. Org. Chem. 14, 873 (1949)
    • (1949) J. Org. Chem. , vol.14 , pp. 873
    • Plati, J.T.1    Schmidt, R.A.2    Wenner, W.3
  • 24
    • 0000749812 scopus 로고
    • The reaction of acetophenone with formaldehyde and methylamine hydrochloride
    • Plati, J. T., Wenner, W., The reaction of acetophenone with formaldehyde and methylamine hydrochloride. J. Org. Chem. 14, 543 (1949)
    • (1949) J. Org. Chem. , vol.14 , pp. 543
    • Plati, J.T.1    Wenner, W.2
  • 25
    • 0024215173 scopus 로고
    • Synthesis and anticonvulsant activity of some new 2(3H)-benzoxazolone derivatives
    • Dalkara, S., Calis, U., Sunal, R., Synthesis and anticonvulsant activity of some new 2(3H)-benzoxazolone derivatives. J. Pharm. Belg. 43, 372 (1988)
    • (1988) J. Pharm. Belg. , vol.43 , pp. 372
    • Dalkara, S.1    Calis, U.2    Sunal, R.3
  • 26
    • 0024211682 scopus 로고
    • The significance of the imidazole ring in anticonvulsant activity of (arylalkyl)imidazoles
    • Calis, U., Dalkara, S., Ertan, M., The significance of the imidazole ring in anticonvulsant activity of (arylalkyl)imidazoles. Arch. Pharm. (Weinheim) 321, 841 (1988)
    • (1988) Arch. Pharm. (Weinheim) , vol.321 , pp. 841
    • Calis, U.1    Dalkara, S.2    Ertan, M.3
  • 27
    • 0026594811 scopus 로고
    • Synthesis and anticonvulsant activity of some new 4-aryl-4-imidazoline-2-one derivatives
    • Calis, U., Dalkara, S., Ertan, M., Synthesis and anticonvulsant activity of some new 4-aryl-4-imidazoline-2-one derivatives. Arzneim.-Forsch./Drug Res. 42 (I), 592 (1992)
    • (1992) Arzneim.-Forsch./Drug Res. , vol.42 , Issue.1 , pp. 592
    • Calis, U.1    Dalkara, S.2    Ertan, M.3
  • 28
    • 0034922216 scopus 로고    scopus 로고
    • Synthesis and evaluation of anticonvulsant activities of some new arylhexahydropyrimidine-2,4-diones
    • Calis, U., Koksal, M., Synthesis and evaluation of anticonvulsant activities of some new arylhexahydropyrimidine-2,4-diones. Arzneim.-Forsch./Drug Res. 51 (II), 523 (2001)
    • (2001) Arzneim.-Forsch./Drug Res. , vol.51 , Issue.2 , pp. 523
    • Calis, U.1    Koksal, M.2
  • 29
    • 0028604559 scopus 로고
    • Synthesis of some N-arylazole acetamide derivatives and their anticonvulsant and antimicrobial activities
    • Ozkanli, F., Dalkara, S., Calis, U. et al., Synthesis of some N-arylazole acetamide derivatives and their anticonvulsant and antimicrobial activities. Arzneim.-Forsch./Drug Res. 44 (II), 920 (1994)
    • (1994) Arzneim.-Forsch./Drug Res. , vol.44 , Issue.2 , pp. 920
    • Ozkanli, F.1    Dalkara, S.2    Calis, U.3
  • 30
    • 0012127211 scopus 로고
    • The preparation of beta-keto amines by Mannich reaction
    • Blicke, F. F., Burckhalter, J. H., The preparation of beta-keto amines by Mannich reaction. J. Am. Chem. Soc. 64, 451 (1942)
    • (1942) J. Am. Chem. Soc. , vol.64 , pp. 451
    • Blicke, F.F.1    Burckhalter, J.H.2
  • 31
    • 0023748452 scopus 로고
    • Evaluation of some azines of aminomethylacetophenones and related quaternary ammonium compounds versus the EMT 6 tumour
    • Dimmock, J. R., Erciyas, E., Kirkpatrick, D. L. et al., Evaluation of some azines of aminomethylacetophenones and related quaternary ammonium compounds versus the EMT6 tumour. Pharmazie 43, 614 (1988)
    • (1988) Pharmazie. , vol.43 , pp. 614
    • Dimmock, J.R.1    Erciyas, E.2    Kirkpatrick, D.L.3
  • 32
    • 0024845339 scopus 로고
    • Synthesis and preliminary study of some ring-substituted arylpropanamines and their quaternary salts
    • Stenlake, J. B., Patrick, G. L., Sneader, W. E., Synthesis and preliminary study of some ring-substituted arylpropanamines and their quaternary salts. Eur. J. Med. Chem. 24, 591 (1989)
    • (1989) Eur. J. Med. Chem. , vol.24 , pp. 591
    • Stenlake, J.B.1    Patrick, G.L.2    Sneader, W.E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.