메뉴 건너뛰기




Volumn 23, Issue 18, 2009, Pages 1719-1730

Synthesis, phytotoxic, cytotoxic, acetylcholinesterase and butrylcholinesterase activities of N,Ń-diaryl unsymmetrically substituted thioureas

Author keywords

Acetylcholinesterase activity; Butrylcholinesterase activity.; Cytotoxicity; N, diaryl unsymmetrically substituted thiourea derivatives; Phytotoxicity

Indexed keywords

2 (2',4' DINITROPHENYL) N PHENYL 1 HYDRAZINECARBOTHIOAMIDE; 2 PHENYL N PHENYL 1 HYDRAZINECARBOTHIOAMIDE; ACETYLCHOLINESTERASE; CHOLINESTERASE; CHOLINESTERASE INHIBITOR; GALANTAMINE; N (1 NAPHTHYL) N' PHENYLTHIOUREA; N (1,5 DIMETHYL 3 OXO 2 PHENYL 2,3 DIHYDRO 1H PYRAZOL 4 YL) N' PHENYLTHIOUREA; N (2 CHLOROPHENYL) N' PHENYLTHIOUREA; N (2 METHOXYPHENYL) N' PHENYLTHIOUREA; N (3 METHOXYPHENYL) N' PHENYLTHIOUREA; N (3 METHYLPHENYL) N' PHENYLTHIOUREA; N (4 BROMOPHENYL) N' PHENYLTHIOUREA; N (4 CHLOROPHENYL) N' PHENYLTHIOUREA; N (4 METHOXYPHENYL) N' PHENYLTHIOUREA; N (4 METHYLPHENYL) N' PHENYLTHIOUREA; N (4 NITROPHENYL) N' PHENYLTHIOUREA; N PHENYL N' (2 PYRIDINYL)THIOUREA; PHYSOSTIGMINE; THIOUREA DERIVATIVE; UNCLASSIFIED DRUG;

EID: 70450189859     PISSN: 14786419     EISSN: 14786427     Source Type: Journal    
DOI: 10.1080/14786410802223778     Document Type: Article
Times cited : (17)

References (41)
  • 1
    • 70450195469 scopus 로고
    • Photochemical process for the preparation of carbodiimides as intermediates for cyanoguanidine epoxy resin hardeners
    • Alder, A. (1989). Photochemical process for the preparation of carbodiimides as intermediates for cyanoguanidine epoxy resin hardeners. European Patent Application EP 307, 361.
    • (1989) European Patent Application EP , vol.307 , pp. 361
    • Alder, A.1
  • 2
    • 12144290205 scopus 로고    scopus 로고
    • Design, synthesis, and biological evaluation of new 8-heterocyclic xanthine derivatives as highly potent and selective human A2B adenosine receptor antagonists
    • Baraldi, P.G., Tabrizi, M.A., Preti, D., Bovero, A., Romagnoli, R., Fruttarolo, F., et al. (2004). Design, synthesis, and biological evaluation of new 8-heterocyclic xanthine derivatives as highly potent and selective human A2B adenosine receptor antagonists. Journal of Medicinal Chemistry, 47, 1434-1447.
    • (2004) Journal of Medicinal Chemistry , vol.47 , pp. 1434-1447
    • Baraldi, P.G.1    Tabrizi, M.A.2    Preti, D.3    Bovero, A.4    Romagnoli, R.5    Fruttarolo, F.6
  • 3
    • 0014019771 scopus 로고
    • Cytokinin activity of some substituted ureas and thioureas
    • (London) Series B
    • Bruce, M.I., & Zwar, J.A. (1966). Cytokinin activity of some substituted ureas and thioureas. Proceedings of the Royal Society (London) Series B, 165, 245-265.
    • (1966) Proceedings of the Royal Society , vol.165 , pp. 245-265
    • Bruce, M.I.1    Zwar, J.A.2
  • 4
    • 0038601097 scopus 로고
    • Chemical structure and plant kinin activity, the activity of urea and thiourea derivatives
    • Bruce, M.I., Zwar, J.A., & Kefford, N.P. (1965). Chemical structure and plant kinin activity, the activity of urea and thiourea derivatives. Life Science, 4, 461-466.
    • (1965) Life Science , vol.4 , pp. 461-466
    • Bruce, M.I.1    Zwar, J.A.2    Kefford, N.P.3
  • 7
    • 70450170395 scopus 로고
    • Intermolecular charge-transfer complexes of arylthiourea derivatives
    • El-Din, A.M. (1986). Intermolecular charge-transfer complexes of arylthiourea derivatives. Bulletin des Sociétés Chimiques Belges, 95(12), 1041-1044.
    • (1986) Bulletin des Sociétés Chimiques Belges , vol.95 , Issue.12 , pp. 1041-1044
    • El-Din, A.M.1
  • 9
    • 0004116672 scopus 로고
    • (3rd ed.). Cambridge: Cambridge University Press
    • Finney, D.J. (1971). Probit analysis (3rd ed.). Cambridge: Cambridge University Press.
    • (1971) Probit Analysis
    • Finney, D.J.1
  • 10
    • 0003905534 scopus 로고
    • Furniss, B.S., Hannaford, A.J., Rogers, V., Smith, P.W.G., & Tatchel, A.R. (Eds.) (Rev., 4th ed.). UK: Longman
    • Furniss, B.S., Hannaford, A.J., Rogers, V., Smith, P.W.G., & Tatchel, A.R. (Eds.) (1986). Vogel's textbook of practical organic chemistry (Rev., 4th ed.). UK: Longman.
    • (1986) Vogel's Textbook of Practical Organic Chemistry
  • 11
    • 0015269530 scopus 로고
    • Inhibitory effect of N-phenyl-N0-aryl or alkylthiourea derivatives on poliovirus multiplication in cell cultures
    • Galabov, A., Shindarov, L., Vasilev, G., & Vasileva, R. (1972). Inhibitory effect of N-phenyl-N0-aryl or alkylthiourea derivatives on poliovirus multiplication in cell cultures. Chemotherapy, 17, 161-174.
    • (1972) Chemotherapy , vol.17 , pp. 161-174
    • Galabov, A.1    Shindarov, L.2    Vasilev, G.3    Vasileva, R.4
  • 12
    • 0001911909 scopus 로고
    • Thioureas in the synthesis of heterocycles
    • A.R. Katritzky & A.J. Boulton (Eds.), Burlington, USA: Academic Press (and therein)
    • Griffin, T.S., Woods, T.S., Klayman, D.L. (1975). Thioureas in the synthesis of heterocycles. In A.R. Katritzky & A.J. Boulton (Eds.), Advances in heterocyclic chemistry (p. 99). Burlington, USA: Academic Press (and therein).
    • (1975) Advances in Heterocyclic Chemistry , pp. 99
    • Griffin, T.S.1    Woods, T.S.2    Klayman, D.L.3
  • 13
    • 0035924235 scopus 로고    scopus 로고
    • Structure-based generation of a new class of potent Cdk4 inhibitors: New de novo design strategy and library design
    • Honma, T., Hayashi, K., Aoyama, T., Hashimoto, N., Machida, T., Fukasawa, K., et al. (2001). Structure-based generation of a new class of potent Cdk4 inhibitors: New De novo design strategy and library design. Journal of Medicinal Chemistry, 44, 4615-4627.
    • (2001) Journal of Medicinal Chemistry , vol.44 , pp. 4615-4627
    • Honma, T.1    Hayashi, K.2    Aoyama, T.3    Hashimoto, N.4    MacHida, T.5    Fukasawa, K.6
  • 14
    • 70450189682 scopus 로고
    • Effect of some synthetic growth regulators on callus tissue growth and developement
    • Izvorska, N., Vasilev, G., Lilov, D., & Belcheva, R. (1986). Effect of some synthetic growth regulators on callus tissue growth and developement. Fiziologiya na Rasteniyata, 12, 41-51.
    • (1986) Fiziologiya Na Rasteniyata , vol.12 , pp. 41-51
    • Izvorska, N.1    Vasilev, G.2    Lilov, D.3    Belcheva, R.4
  • 16
    • 0004975591 scopus 로고
    • Quantitative structure-activity relations for fungicidal N-phenyl-N0-alkyl- and N-phenyl-N0-arylthioureas
    • Krause, G., Franke, R., & Vasilev, G.N. (1979). Quantitative structure-activity relations for fungicidal N-phenyl-N0-alkyl- and N-phenyl-N0-arylthioureas. Biochemie und Physiologie der Pflanzen, 174, 128-138.
    • (1979) Biochemie und Physiologie der Pflanzen , vol.174 , pp. 128-138
    • Krause, G.1    Franke, R.2    Vasilev, G.N.3
  • 18
    • 0016332351 scopus 로고
    • Chemical structure and cytokinin activity of some new phenylthiourea derivatives and their effect on nitrogen metabolism in barley seedlings
    • Mashev, N., & Vasilev, G. (1974a). Chemical structure and cytokinin activity of some new phenylthiourea derivatives and their effect on nitrogen metabolism in barley seedlings. Fiziologiya na Rasteniyata, 1, 19-29.
    • (1974) Fiziologiya Na Rasteniyata , vol.1 , pp. 19-29
    • Mashev, N.1    Vasilev, G.2
  • 19
    • 70450184550 scopus 로고
    • Chemical structure and cytokinin-like activity of certain derivatives of phenylthiourea and their influence on the nitrogen metabolism in barley seedlings
    • Mashev, N., & Vasilev, G. (1974b). Chemical structure and cytokinin-like activity of certain derivatives of phenylthiourea and their influence on the nitrogen metabolism in barley seedlings. Doklady Sel'skokhozyaistvennoi Akademii im, 7, 11-15.
    • (1974) Doklady sel'Skokhozyaistvennoi Akademii im , vol.7 , pp. 11-15
    • Mashev, N.1    Vasilev, G.2
  • 20
    • 84981666154 scopus 로고
    • Search for new insecticides. I. Study of pyridyl substituted thioureas as insecticides
    • Mathur, S.P. (1976). Search for new insecticides. I. Study of pyridyl substituted thioureas as insecticides. Revista Latinoamericana De Quimica, 7, 141-142.
    • (1976) Revista Latinoamericana de Quimica , vol.7 , pp. 141-142
    • Mathur, S.P.1
  • 21
    • 0000345763 scopus 로고
    • Bench-top bioassays for the discovery of bioactive natural products: An update
    • Atta-ur-Rahman (Ed.) Amsterdam: Elsevier Science Publishers B.V.
    • McLaughlin, J.L., Chang, C.J., & Smith, D.L. (1991). "Bench-top" bioassays for the discovery of bioactive natural products: An update. In Atta-ur-Rahman (Ed.), Studies in natural product chemistry (Part B, Vol. 9, pp. 383-409).
    • (1991) Studies in Natural Product Chemistry , vol.9 , Issue.PART B , pp. 383-409
    • McLaughlin, J.L.1    Chang, C.J.2    Smith, D.L.3
  • 23
    • 0008245197 scopus 로고
    • Phenylisothiocyanate and ortho-tolylisothiocyanate as reagents for primary aromatic amines
    • Otterbacher, T., & Whitemore, F.C. (1929). Phenylisothiocyanate and ortho-tolylisothiocyanate as reagents for primary aromatic amines. Journal of the American Chemical Society, 51, 1909-1911.
    • (1929) Journal of the American Chemical Society , vol.51 , pp. 1909-1911
    • Otterbacher, T.1    Whitemore, F.C.2
  • 24
    • 0031934494 scopus 로고    scopus 로고
    • Antifungal activity of 1,3- disubstituted symmetrical and unsymmetrical thioureas
    • Ramadas, K., Suresh, G., Janarthanan, N., & Masilamani, S. (1998). Antifungal activity of 1,3- disubstituted symmetrical and unsymmetrical thioureas. PesticiDe Science, 52, 145-151.
    • (1998) PesticiDe Science , vol.52 , pp. 145-151
    • Ramadas, K.1    Suresh, G.2    Janarthanan, N.3    Masilamani, S.4
  • 25
    • 0021915057 scopus 로고
    • Synthesis and spectroscopic properties of some new N,N0- disubstituted thioureas of potential biological interest
    • Sarkis, G.Y., & Faisal, E.D. (1985). Synthesis and spectroscopic properties of some new N,N0- disubstituted thioureas of potential biological interest. Journal of Heterocyclic Chemistry, 22, 137-140.
    • (1985) Journal of Heterocyclic Chemistry , vol.22 , pp. 137-140
    • Sarkis, G.Y.1    Faisal, E.D.2
  • 30
    • 70450162726 scopus 로고    scopus 로고
    • Synthesis and antifungal and antibacterial effect of thiourea derivatives
    • Truong, P., & Ngo, D.T.H. (1999). Synthesis and antifungal and antibacterial effect of thiourea derivatives. Ta- p ch?́ Du'o- 'c ho- c, 12, 14-16.
    • (1999) Tap Ch?́ du'O'c Hoc , vol.12 , pp. 14-16
    • Truong, P.1    Ngo, D.T.H.2
  • 31
    • 70450193321 scopus 로고
    • Synthesis, herbicidal, growth-regulating activities of some coordination compounds of N-phenyl-N0-2-pyridylthiourea
    • Vasilev, G., & Davarski, K. (1986). Synthesis, herbicidal, growth-regulating activities of some coordination compounds of N-phenyl-N0-2-pyridylthiourea. Doklady Bolgarskoi Akademii Nauk, 39, 103-106.
    • (1986) Doklady Bolgarskoi Akademii Nauk , vol.39 , pp. 103-106
    • Vasilev, G.1    Davarski, K.2
  • 32
    • 70450187594 scopus 로고
    • Chemical structure and herbicidal activity of certain esters of m- and p-(ethylthioureido)benzoic acids and of 3-ethyl-4-oxo-2-thiono-1 2 3,4- tetrahydroquinazoline
    • Vasilev, G., Iliev, L.K., & Vasileva, R.T. (1969). Chemical structure and herbicidal activity of certain esters of m- and p-(ethylthioureido)benzoic acids and of 3-ethyl-4-oxo-2-thiono-1,2,3,4- tetrahydroquinazoline. Doklady Bolgarskoi Akademii Nauk, 22, 1031-1034.
    • (1969) Doklady Bolgarskoi Akademii Nauk , vol.22 , pp. 1031-1034
    • Vasilev, G.1    Iliev, L.K.2    Vasileva, R.T.3
  • 33
    • 0017965002 scopus 로고
    • Synthesis, structure and cytokinin-like activity of N-alkyl- and phenyl-N0-halophenylthioureas
    • Vasilev, G., & Ionova, P. (1978). Synthesis, structure and cytokinin-like activity of N-alkyl- and phenyl-N0-halophenylthioureas. Pharmazie, 33, 270-273.
    • (1978) Pharmazie , vol.33 , pp. 270-273
    • Vasilev, G.1    Ionova, P.2
  • 34
    • 0005697496 scopus 로고
    • Synthesis and herbicidal and growth regulating activity of some N-alkyl- and phenyl-N0-pyridylthioureas
    • Vasilev, G., & Ionova, P. (1984). Synthesis and herbicidal and growth regulating activity of some N-alkyl- and phenyl-N0-pyridylthioureas. Fiziologiya na Rasteniyata, 10, 40-49.
    • (1984) Fiziologiya Na Rasteniyata , vol.10 , pp. 40-49
    • Vasilev, G.1    Ionova, P.2
  • 35
    • 0037586908 scopus 로고
    • Synthesis, chemical structure and cytokinin-like activity of some derivatives of N-phenyl-N0-alkyl or arylthiourea and their influence on the nitrogen metabolism in barley seedlings
    • Vasilev, G., & Mashev, N.P. (1974). Synthesis, chemical structure and cytokinin-like activity of some derivatives of N-phenyl-N0-alkyl or arylthiourea and their influence on the nitrogen metabolism in barley seedlings. Biochemie und Physiologie der Pflanzen, 165, 467-478.
    • (1974) Biochemie und Physiologie der Pflanzen , vol.165 , pp. 467-478
    • Vasilev, G.1    Mashev, N.P.2
  • 37
    • 0004944418 scopus 로고
    • Chemical structure and fungicidal effect of several derivatives of N-phenyl-N0-alkyl- or aryl thiourea
    • Vasilev, G., & Tomaleva, Z. (1973). Chemical structure and fungicidal effect of several derivatives of N-phenyl-N0-alkyl- or aryl thiourea. Archiv für Phytopathologie und Pflanzenschutz, 9, 309-320.
    • (1973) Archiv für Phytopathologie und Pflanzenschutz , vol.9 , pp. 309-320
    • Vasilev, G.1    Tomaleva, Z.2
  • 38
    • 84917792408 scopus 로고
    • Synthesis, chemical structure, and antiviral effect of some derivatives of N-phenyl-N0-aryl or alkylthioureas on the picornaviruses
    • Vasilev, G., Vasileva, R., Galabov, A., & Shindarov, L. (1972). Synthesis, chemical structure, and antiviral effect of some derivatives of N-phenyl-N0-aryl or alkylthioureas on the picornaviruses. Doklady Sel'skokhozyaistvennoi Akademii im, 5, 311-321.
    • (1972) Doklady sel'Skokhozyaistvennoi Akademii im , vol.5 , pp. 311-321
    • Vasilev, G.1    Vasileva, R.2    Galabov, A.3    Shindarov, L.4
  • 39
    • 0038722946 scopus 로고    scopus 로고
    • Synthesis, chemical structure and cytokinin activity of some N-alkyl and phenyl-N0-hydroxy-, methoxy- and ethoxyphenylthiourea
    • Vassilev, G., & Vassilev, N.G. (2002). Synthesis, chemical structure and cytokinin activity of some N-alkyl and phenyl-N0-hydroxy-, methoxy- and ethoxyphenylthiourea. Oxidation Communications, 25, 608-612.
    • (2002) Oxidation Communications , vol.25 , pp. 608-612
    • Vassilev, G.1    Vassilev, N.G.2
  • 40
    • 15644373566 scopus 로고    scopus 로고
    • 2-Nitrophenylcarbamoyl-(S)-prolyl-(S)-3-(2-naphthyl)alanyl-N-benzyl-N- methylamiDe (SDZ NKT 343), a potent human NK1 tachykinin receptor antagonist with good oral analgesic activity in chronic pain models
    • Walpole, C., Ko, S.Y., Brown, M., Beattie, D., Campbell, E., Dickenson, F., et al. (1998). 2-Nitrophenylcarbamoyl-(S)-prolyl-(S)-3-(2-naphthyl)alanyl-N- benzyl-N-methylamiDe (SDZ NKT 343), a potent human NK1 tachykinin receptor antagonist with good oral analgesic activity in chronic pain models. Journal of Medicinal Chemistry, 41, 3159-3173.
    • (1998) Journal of Medicinal Chemistry , vol.41 , pp. 3159-3173
    • Walpole, C.1    Ko, S.Y.2    Brown, M.3    Beattie, D.4    Campbell, E.5    Dickenson, F.6
  • 41
    • 0033587026 scopus 로고    scopus 로고
    • Synthesis of novel phenserine-based-selective inhibitors of butyrylcholinestrase for Alzheimer's disease
    • Yu, Q.-S., Holloway, H.W., Utsuki, T., Brossi, A., & Greig, N.H. (1999). Synthesis of novel phenserine-based-selective inhibitors of butyrylcholinestrase for Alzheimer's disease. Journal of Medicinal Chemistry, 42, 1855-1861.
    • (1999) Journal of Medicinal Chemistry , vol.42 , pp. 1855-1861
    • Yu, Q.-S.1    Holloway, H.W.2    Utsuki, T.3    Brossi, A.4    Greig, N.H.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.