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Volumn 36, Issue 12, 2013, Pages 1465-1479

Design, synthesis and molecular docking of some new 1,2,4- triazolobenzimidazol-3-yl acetohydrazide derivatives with anti-inflammatory- analgesic activities

Author keywords

1,2,4 Triazolobenzimidazole; Anti inflammatory analgesic; COX enzyme; Molecular docking; Ulcerogenecity

Indexed keywords

2 (ACETYLSULFANYL) 5 [[2 (METHYLSULFANYL) 3H 1,2,4 TRIAZOLO(1,5 A)BENZIMIDAZOL 3 YL]METHYL] 1,3,4 OXADIAZOLE; 2 (N PROPYLSULFANYL) 5 [[2 (METHYLSULFANYL) 3H 1,2,4 TRIAZOLO(1,5 A)BENZIMIDAZOL 3 YL]METHYL] 1,3,4 OXADIAZOLE; 2 [(2 PHENYLETHYL)SULFANYL] 5 [[2 (METHYLSULFANYL) 3H 1,2,4 TRIAZOLO(1,5 A)BENZIMIDAZOL 3 YL]METHYL] 1,3,4 OXADIAZOLE; 4 AMINO 3 [(2 PHENYLETHYL)SULFANYL] 5 [[2 (METHYLSULFANYL) 3H 1,2,4 TRIAZOLO(1,5 A)BENZIMIDAZOL 3 YL]METHYL] 4H 1,2,4 TRIAZOLE; 4 AMINO 5 [[2 (METHYLSULFANYL) 3H 1,2,4 TRIAZOLO(1,5 A)BENZIMIDAZOL 3 YL]METHYL] 2,4 DIHYDRO 3H 1,2,4 TRIAZOLE 3 THIONE; 5 [[2 (METHYLSULFANYL) 3H 1,2,4 TRIAZOLO(1,5 A)BENZIMIDAZOL 3 YL]METHYL] 1,3,4 OXADIAZOLE 2(3H) THIONE; [2 (METHYLSULFANYL) 3H 1,2,4 TRIAZOLO(1,5 A)BENZIMIDAZOLE 3 YL] ACETATE; [2 (METHYLSULFANYL) 3H 1,2,4 TRIAZOLO(1,5 A)BENZIMIDAZOLE 3 YL] N' (1 PHENYLETHYLIDENE)ACETOHYDRAZIDE; [2 (METHYLSULFANYL) 3H 1,2,4 TRIAZOLO(1,5 A)BENZIMIDAZOLE 3 YL] N' (3 CHLOROPHENYLMETHYLIDENE)ACETOHYDRAZIDE; [2 (METHYLSULFANYL) 3H 1,2,4 TRIAZOLO(1,5 A)BENZIMIDAZOLE 3 YL] N' (4 ISOPROPYLPHENYLMETHYLIDENE)ACETOHYDRAZIDE; [2 (METHYLSULFANYL) 3H 1,2,4 TRIAZOLO(1,5 A)BENZIMIDAZOLE 3 YL] N' (4 NITROPHENYLMETHYLIDENE)ACETOHYDRAZIDE; [2 (METHYLSULFANYL) 3H 1,2,4 TRIAZOLO(1,5 A)BENZIMIDAZOLE 3 YL] N' [1 (4 BROMOPHENYL)ETHYLIDENE]ACETOHYDRAZIDE; [2 (METHYLSULFANYL) 3H 1,2,4 TRIAZOLO(1,5 A)BENZIMIDAZOLE 3 YL] N' [1 (4 CHLOROPHENYL)ETHYLIDENE]ACETOHYDRAZIDE; [2 (METHYLSULFANYL) 3H 1,2,4 TRIAZOLO(1,5 A)BENZIMIDAZOLE 3 YL] N' [1 (4 METHOXYPHENYL)ETHYLIDENE]ACETOHYDRAZIDE; [2 (METHYLSULFANYL) 3H 1,2,4 TRIAZOLO(1,5 A)BENZIMIDAZOLE 3 YL]ACETOHYDRAZIDE; ANALGESIC AGENT; ANTIINFLAMMATORY AGENT; HYDRAZIDE DERIVATIVE; INDOMETACIN; METHYL[[5 [[2 (METHYLSULFANYL) 3H 1,2,4 TRIAZOLO(1,5 A)BENZIMIDAZOL 3 YL]METHYL] 1,3,4 OXADIAZOL 2 YL]SULFANYL]ACETATE; N (4 BROMOPHENYL) 2 [[5 [[2 (METHYLSULFANYL) 3H 1,2,4 TRIAZOLO(1,5 A)BENZIMIDAZOL 3 YL]METHYL] 1,3,4 OXADIAZOL 2 YL]SULFANYL]ACETAMIDE; N [3 [(2 PHENYLETHYL)SULFANYL] 5 [[2 (METHYLSULFANYL) 3H 1,2,4 TRIAZOLO(1,5 A)BENZIMIDAZOL 3 YL]METHYL] 4H 1,2,4 TRIAZOL 4 YL]4 CHLOROBENZAMIDE; UNCLASSIFIED DRUG;

EID: 84890800650     PISSN: 02536269     EISSN: 19763786     Source Type: Journal    
DOI: 10.1007/s12272-013-0153-z     Document Type: Article
Times cited : (33)

References (35)
  • 1
    • 84858039209 scopus 로고    scopus 로고
    • Synthesis of some new S-alkylated 1,2,4-triazoles, their mannich bases and their biological activities
    • 22045469 10.1002/ardp.201100128 1:CAS:528:DC%2BC3MXhsVShs7zO
    • Alam, M.M., S. Nazreen, S. Haider, S. Shafi, M.S. Yar, H. Hamid, and M.S. Alam. 2012. Synthesis of some new S-alkylated 1,2,4-triazoles, their mannich bases and their biological activities. Archiv der Pharmazie 345: 203-214.
    • (2012) Archiv der Pharmazie , vol.345 , pp. 203-214
    • Alam, M.M.1    Nazreen, S.2    Haider, S.3    Shafi, S.4    Yar, M.S.5    Hamid, H.6    Alam, M.S.7
  • 2
    • 33847666494 scopus 로고    scopus 로고
    • Synthesis and evaluation of anti-inflammatory, analgesic, ulcerogenic and lipid peroxidation properties of ibuprofen derivatives
    • DOI 10.2478/v10007-007-0003-y
    • Amir, M., and S. Kumar. 2007. Synthesis and evaluation of anti-inflammatory, analgesic, ulcerogenic and lipid peroxidation properties of ibuprofen derivatives. Acta Pharmaceutica 57: 31-45. (Pubitemid 46361946)
    • (2007) Acta Pharmaceutica , vol.57 , Issue.1 , pp. 31-45
    • Amir, M.1    Kumar, S.2
  • 3
    • 77951874429 scopus 로고    scopus 로고
    • Synthesis and antimicrobial activities of some new 1,2,4-triazole derivatives
    • 20428053 10.3390/molecules15042427
    • Bektaş, H., N. Karaali, D. Şahin, A. Demirbaş, Ş.A. Karaoglu, and N. Demirbaş. 2010. Synthesis and antimicrobial activities of some new 1,2,4-triazole derivatives. Molecules 15: 2427-2438.
    • (2010) Molecules , vol.15 , pp. 2427-2438
    • Bektaş, H.1    Karaali, N.2    Şahin, D.3    Demirbaş, A.4    Karaoglu, Ş.5    Demirbaş, N.6
  • 4
    • 0022485090 scopus 로고
    • 7-aroyl-2,3-dihydrobenzo[b]furan-3-carboxylic acids and 7-benzoyl-2,3-dihydrobenzo[b]thiophene-3-carboxylic acids as analgesic agents
    • Boyle, E.A., F.R. Mangan, R.E. Markwell, S.A. Smith, M.J. Thomson, R.W. Ward, and P.A. Wyman. 1986. 7-Aroyl-2,3-dihydrobenzo[b]furan-3-carboxylic acids and 7-benzoyl-2,3-dihydrobenzo[b]thiophene-3-carboxylic acids as analgesic agents. Journal of Medicinal Chemistry 29: 894-898. (Pubitemid 16068794)
    • (1986) Journal of Medicinal Chemistry , vol.29 , Issue.6 , pp. 894-898
    • Boyle, E.A.1    Mangan, F.R.2    Markwell, R.E.3
  • 5
    • 40049096127 scopus 로고    scopus 로고
    • Synthesis, antifungal activity and CoMFA analysis of novel 1,2,4-triazolo[1,5-a]pyrimidine derivatives
    • DOI 10.1016/j.ejmech.2007.04.021, PII S0223523407002152
    • Chen, Q., X. Zhu, L. Jiang, Z. Liu, and G. Yang. 2008. Synthesis, antifungal activity and CoMFA analysis of novel 1,2,4-triazolo[1,5-a]pyrimidine derivatives. European Journal of Medicinal Chemistry 43: 595-603. (Pubitemid 351323990)
    • (2008) European Journal of Medicinal Chemistry , vol.43 , Issue.3 , pp. 595-603
    • Chen, Q.1    Zhu, X.-L.2    Jiang, L.-L.3    Liu, Z.-M.4    Yang, G.-F.5
  • 6
    • 15244359733 scopus 로고    scopus 로고
    • Synthesis and antimicrobial activities of some new [1,2,4]triazolo[3,4-b] [1,3,4]thiadiazoles and [1,2,4]triazolo[3,4-b] [1,3,4]thiadiazines
    • General Papers
    • Demirbas, N.; Demirbas, A.; Karaoglu, S.A, and Çelik, E. 2005. Synthesis and antimicrobial activities of some new 1,2,4-triazole[3,4-b]1,3,4- thiadiazoles and 1,2,4-triazolo[3,4-b]1,3,4-thiadiazines. ARKIVOC i:75-91. (Pubitemid 40390032)
    • (2005) Arkivoc , vol.2005 , Issue.1 , pp. 75-91
    • Demirbas, N.1    Demirbas, A.2    Karaoglu, S.A.3    Celik, E.4
  • 8
    • 0037429108 scopus 로고    scopus 로고
    • Solid state and solution conformation of 2-pyridinecarboxylic acid hydrazides: A new structural motif for foldamers
    • DOI 10.1016/S0040-4039(02)02881-2, PII S0040403902028812
    • Garric, J., J. Lèger, A. Grelard, M. Ohkita, and I. Huc. 2003. Solid state and solution conformation of 2-pyridinecarboxylic acid hydrazides: A new structural motif for foldamers. Tetrahedron Letters 44: 1421-1424. (Pubitemid 36164921)
    • (2003) Tetrahedron Letters , vol.44 , Issue.7 , pp. 1421-1424
    • Garric, J.1    Leger, J.-M.2    Grelard, A.3    Ohkita, M.4    Huc, I.5
  • 10
    • 84944193623 scopus 로고
    • In the chemistry of amides
    • J. Zabieky (eds) Wiley Interscience New York
    • Homer, R.B., and C.D. Johnson. 1970. In the chemistry of amides. In Patai Series, ed. J. Zabieky, 225. New York: Wiley Interscience.
    • (1970) Patai Series , pp. 225
    • Homer, R.B.1    Johnson, C.D.2
  • 11
    • 0023572184 scopus 로고
    • Synthesis and antiinflammatory activities of 3-(3,5-di-tert-butyl-4- hydroxybenzylidene)pyrrolidin-2-ones
    • Ikuta, H., H. Shirota, S. Kobayashi, Y. Yamagishi, K. Yamada, I. Yamatsu, and K. Katayama. 1987. Synthesis and anti-inflammatory activities of 3-(3,5-di-tert-butyl-4-hydroxy benzylidene)pyrrolidin-2-ones. Journal of Medicinal Chemistry 30: 1995-1998. (Pubitemid 18046053)
    • (1987) Journal of Medicinal Chemistry , vol.30 , Issue.11 , pp. 1995-1998
    • Ikuta, H.1    Shirota, H.2    Kobayashi, S.3    Yamagishi, Y.4    Yamada, K.5    Yamatsu, I.6    Katayama, K.7
  • 12
    • 67651152598 scopus 로고    scopus 로고
    • Synthesis and pharmacological evaluation of 1,3,4-oxadiazole bearing bis(heterocyle) derivatives as anti-inflammatory and analgesic agents
    • 19423197 10.1016/j.ejmech.2009.04.006 1:CAS:528:DC%2BD1MXptlersLY%3D
    • Jayashankar, B., K.M.L. Rai, N. Baskaran, and H.S. Sathish. 2009. Synthesis and pharmacological evaluation of 1,3,4-oxadiazole bearing bis(heterocyle) derivatives as anti-inflammatory and analgesic agents. European Journal of Medicinal Chemistry 44: 3898-3902.
    • (2009) European Journal of Medicinal Chemistry , vol.44 , pp. 3898-3902
    • Jayashankar, B.1    Rai, K.M.L.2    Baskaran, N.3    Sathish, H.S.4
  • 13
    • 34047221878 scopus 로고    scopus 로고
    • Synthesis and antimicrobial activities of some novel 1,2,4-triazolo[3,4- b]-1,3,4-thiadiazoles and 1,2,4-triazolo[3,4-b]-1,3,4-thiadiazines carrying thioalkyl and sulphonyl phenoxy moieties
    • DOI 10.1016/j.ejmech.2006.10.010, PII S0223523406003849
    • Karabasanagouda, T., A.V. Adhikari, and N.S. Shetty. 2007. Synthesis and antimicrobial activities of some novel 1,2,4-triazolo[3,4-b]1,3,4thiadiazoles and 1,2,4-triazolo[3,4-b]1,3,4-thiadiazines carrying thioalkyl and sulphonyl phenoxy moieties. European Journal of Medicinal Chemistry 42: 521-529. (Pubitemid 46533874)
    • (2007) European Journal of Medicinal Chemistry , vol.42 , Issue.4 , pp. 521-529
    • Karabasanagouda, T.1    Adhikari, A.V.2    Shetty, N.S.3
  • 14
    • 34347236781 scopus 로고
    • Synthesis and antihypertensive activity of some 9H-1,2,4-triazolo[4,3-a] benzimidazoles
    • through Chem. Abstr., 102, 6319g, (1985)
    • Liu, K. C.; Chang, J. L. and Chen, C. F., Synthesis and antihypertensive activity of some 9H-1,2,4-triazolo[4,3-a]benzimidazoles, T'ai-wan Yao Hsueh Tsa Chih, 36 (1), 33-40, (1984); through Chem. Abstr., 102, 6319g, (1985).
    • (1984) T'Ai-wan Yao Hsueh Tsa Chih , vol.36 , Issue.1 , pp. 33-40
    • Liu, K.C.1    Chang, J.L.2    Chen, C.F.3
  • 15
    • 32844460667 scopus 로고    scopus 로고
    • Synthesis of 1-acyl-2-alkylthio-1,2,4-triazolobenzimidazoles with antifungal, anti-inflammatory and analgesic effects
    • Mohammad, B.G., A.M. Abdel-Alim, and M.A. Hussein. 2006a. Synthesis of 1-acyl-2-alkylthio-1,2,4-triazolobenzimidazoles with antifungal, anti-inflammatory and analgesic. Acta Pharmaceutica 56: 31-48. (Pubitemid 43253971)
    • (2006) Acta Pharmaceutica , vol.56 , Issue.1 , pp. 31-48
    • Mohamed, B.G.1    Abdel-Alim, A.-A.M.2    Hussein, M.A.3
  • 16
    • 33144465711 scopus 로고    scopus 로고
    • Synthesis and antimicrobial activity of some new 1-alkyl-2-alkylthio-1,2, 4- triazolobenzimidazole derivatives
    • Mohammad, B.G., M.A. Hussein, A.M. Abdel-Alim, and M. Hashem. 2006b. Synthesis and antimicrobial activity of some new 1-alkyl-2-alkylthio-1,2,4- triazolobenzimidazole derivatives. Archives of Pharmacal Research 29: 26-33. (Pubitemid 43268419)
    • (2006) Archives of Pharmacal Research , vol.29 , Issue.1 , pp. 26-33
    • Mohamed, B.G.1    Hussein, M.A.2    Abdel-Alim, A.-A.M.3    Hashem, M.4
  • 17
    • 84862884655 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of some benzimidazo-1,2,4-triazole derivatives as antimicrobial and anti-inflammatory Agents
    • 10.1248/bpb.34.77 1:CAS:528:DC%2BC38XmtFGmsQ%3D%3D
    • Mohammed, A.F., M.A. Hussein, S.G. Abdel-Moty, and A.M. Abdel-Alim. 2011. Synthesis and biological evaluation of some benzimidazo-1,2,4-triazole derivatives as antimicrobial and anti-inflammatory Agents. Bulletin of Pharmaceutical Sciences 34(1): 77-92.
    • (2011) Bulletin of Pharmaceutical Sciences , vol.34 , Issue.1 , pp. 77-92
    • Mohammed, A.F.1    Hussein, M.A.2    Abdel-Moty, S.G.3    Abdel-Alim, A.M.4
  • 18
    • 0004313709 scopus 로고    scopus 로고
    • version 2009.06. Chemical Computing Group, Inc. Montreal, Quebec, Canada Accessed June 2012
    • Molecular Operating Environment (MOE). 2009. version 2009.06. Chemical Computing Group, Inc. Montreal, Quebec, Canada, http://www.chemcomp.com. Accessed June 2012.
    • (2009) Molecular Operating Environment (MOE)
  • 19
    • 0028352765 scopus 로고
    • Anti-inflammatory activity of substituted 1,3,4-oxadiazoles
    • DOI 10.1002/jps.2600830226
    • Nargund, L.V., G.R. Reddy, and V. Hariprasad. 1994. Anti-inflammatory activity of substituted 1,3,4-oxadiazoles. Journal of Pharmaceutical Sciences 83(2): 246-248. (Pubitemid 24224186)
    • (1994) Journal of Pharmaceutical Sciences , vol.83 , Issue.2 , pp. 246-248
    • Nargund, L.V.G.1    Reddy, G.R.N.2    Hariprasad, V.3
  • 20
    • 84890790954 scopus 로고    scopus 로고
    • 13thed. Merck Research laboratories New Jersey: Whitehouse Station
    • O'Neil, M. J., Smith, A. and Heckelman, P. E. 2001. In The Merck Index, 13thed. Merck Research laboratories, 787. New Jersey: Whitehouse Station.
    • (2001) The Merck Index , vol.787
    • O'Neil, M.J.1    Smith, A.2    Heckelman, P.E.3
  • 21
    • 0035439443 scopus 로고    scopus 로고
    • Synthesis and receptor docking studies of N-substituted indole-2-carboxylic acid esters as a search for COX-2 selective enzyme inhibitors
    • DOI 10.1016/S0223-5234(01)01258-2
    • Olgen, S., E. Akaho, and D. Nebioglu. 2001. Synthesis and receptor docking studies of N-substituted indole-2-carboxylic acid esters as a search for COX-2 selective enzyme inhibitors. European Journal of Medicinal Chemistry 36: 747-770. (Pubitemid 32973867)
    • (2001) European Journal of Medicinal Chemistry , vol.36 , Issue.9 , pp. 747-770
    • Olgen, S.1    Akaho, E.2    Nebioglu, D.3
  • 22
    • 62549093538 scopus 로고    scopus 로고
    • Synthesis and bioassay of a new class of heterocycles pyrrolyl oxadiazoles/thiadiazoles/triazoles
    • 18547683 10.1016/j.ejmech.2008.04.003 1:CAS:528:DC%2BD1MXjsl2gsbg%3D
    • Padmavathi, V., A.V. Nagendra Mohan, P. Thriveni, and A. Shazia. 2009. Synthesis and bioassay of a new class of heterocycles pyrrolyl oxadiazoles/thiadiazoles/triazoles. European Journal of Medicinal Chemistry 44: 2313-2321.
    • (2009) European Journal of Medicinal Chemistry , vol.44 , pp. 2313-2321
    • Padmavathi, V.1    Nagendra Mohan, A.V.2    Thriveni, P.3    Shazia, A.4
  • 23
    • 0000544558 scopus 로고
    • Conformational behavior and E/Z isomerization of N-acyl and N-aroylhydrazones
    • 10.1016/S0040-4020(01)87332-4 1:CAS:528:DyaL2sXhsFGls7k%3D
    • Palla, G., G. Predieri, and P. Domiano. 1986. Conformational behavior and E/Z isomerization of N-acyl and N-aroylhydrazones. Tetrahedron 42(13): 3649-3654.
    • (1986) Tetrahedron , vol.42 , Issue.13 , pp. 3649-3654
    • Palla, G.1    Predieri, G.2    Domiano, P.3
  • 24
    • 0036136418 scopus 로고    scopus 로고
    • Molecular modelling of the differential interaction between several non-steroidal anti-inflammatory drugs and human prostaglandin endoperoxide H synthase-2 (h-PGHS-2)
    • DOI 10.1016/S1093-3263(01)00133-4, PII S1093326301001334
    • Pouplana, R., J.J. Lozano, and J. Ruiz. 2002. Molecular modeling of the differential interaction between several non-steroidal anti-infalmmatory drugs and human prostaglandin endoperoxide H synthase-2 (h-PGHS-2). Journal of Molecular Graphics and Modeling 20: 329-343. (Pubitemid 34019230)
    • (2002) Journal of Molecular Graphics and Modelling , vol.20 , Issue.4 , pp. 329-343
    • Pouplana, R.1    Lozano, J.J.2    Ruiz, J.3
  • 25
    • 34548531844 scopus 로고    scopus 로고
    • Anti-inflammatory, analgesic, ulcerogenic activities of some new non-acidic diclofenac and 1,3,4-oxadiazole derivatives in animal models
    • Raut, M.K., S.V. Bhandari, K.G. Bothara, A.A. Patil, and A.P. Sarkate. 2007. Anti-inflammatory, analgesic, ulcerogenic activities of some new non-acidic diclofenac and 1,3,4-oxadiazole derivatives in animal models. Pharmacologyonline 2: 172-186. (Pubitemid 47382448)
    • (2007) Pharmacologyonline , vol.2 , pp. 172-186
    • Raut, M.K.1    Bhandari, S.V.2    Bothara, K.G.3    Patil, A.A.4    Sarkate, A.P.5
  • 26
    • 84907616297 scopus 로고
    • Improved syntheses of 5-substituted-4-amino-3-mercapto-(4H)-1,2,4- triazoles
    • 10.1002/jhet.5570130450 1:CAS:528:DyaE2sXltlOn
    • Reid, J.R., and N.D. Heindel. 1976. Improved syntheses of 5-substituted-4-amino-3-mercapto-(4H)-1,2,4-triazoles. Journal of Heterocyclic Chemistry 13: 925-926.
    • (1976) Journal of Heterocyclic Chemistry , vol.13 , pp. 925-926
    • Reid, J.R.1    Heindel, N.D.2
  • 28
    • 85069129975 scopus 로고
    • Synthesis of some new benzimidazole derivatives with potential anti-microbial activity
    • Sharaf El-Din, N. 1995. Synthesis of some new benzimidazole derivatives with potential anti-microbial activity. Zagazig Journal of Pharmaceutical Science 4(2): 198-203.
    • (1995) Zagazig Journal of Pharmaceutical Science , vol.4 , Issue.2 , pp. 198-203
    • Sharaf El-Din, N.1
  • 30
    • 2542432180 scopus 로고    scopus 로고
    • New class of potent antinociceptive and antiplatelet 10H-phenothiazine-1- acylhydrazone derivatives
    • DOI 10.1016/j.bmc.2004.04.009, PII S0968089604002858
    • Silva, G.A., L.M. Costa, F.C. Brito, A.L. Miranda, E.J. Barreito, and C.A. Fragra. 2004. New class of potent antinociceptive and antiplatelet 10H-phenothiazine-1-acylhydrazone derivatives. Bioorganic & Medicinal Chemistry Letters 12: 3149-3158. (Pubitemid 38680704)
    • (2004) Bioorganic and Medicinal Chemistry , vol.12 , Issue.12 , pp. 3149-3158
    • Silva, G.A.1    Costa, L.M.M.2    Brito, F.C.F.3    Miranda, A.L.P.4    Barreiro, E.J.5    Fraga, C.A.M.6
  • 31
    • 0033635665 scopus 로고    scopus 로고
    • Search for antihistamine drugs among imidazobenzimidazoles and triazolobenzimidazoles
    • 10.1007/BF02524356 1:CAS:528:DC%2BD3cXosF2lsLw%3D
    • Spasov, A.A., M.V. Chernikov, V.A. Anisimova, T.A. KuÅmenko, and M.M. Osipova. 2000. Search for antihistamine drugs among imidazobenzimidazoles and triazolobenzimidazoles. Pharmaceutical Chemistry Journal 34(2): 48-52.
    • (2000) Pharmaceutical Chemistry Journal , vol.34 , Issue.2 , pp. 48-52
    • Spasov, A.A.1    Chernikov, M.V.2    Anisimova, V.A.3    Kuåmenko, T.A.4    Osipova, M.M.5
  • 32
    • 0345411644 scopus 로고    scopus 로고
    • Antiulcer effect of the N- and 0-β-D-glucopyranosides of 5- aminosalicylic acid
    • DOI 10.1002/(SICI)1521-4184(19999)332:9<321::AID-ARDP321>3.0.CO;2-A
    • Sztaricskai, F., I.E. Takács, F. Pusztai, G. Szabó, and I. Csípõ. 1999. Antiulcer effect of the N- and O-β-d- glucopyranosides of 5-aminosalicylic acid. Archiv der Pharmazie 332: 321-326. (Pubitemid 29446518)
    • (1999) Archiv der Pharmazie , vol.332 , Issue.9 , pp. 321-326
    • Sztaricskai, F.1    Takacs, I.E.2    Pusztai, F.3    Szabo, G.4    Csipo, I.5
  • 34
    • 0342647359 scopus 로고    scopus 로고
    • 6-Benzylidenethiazolo[3,2-b]-1,2,4-triazole-5(6H)-ones substituted with ibuprofen: Synthesis, characterization and evaluation of anti-inflammatory activity
    • DOI 10.1016/S0223-5234(00)00157-4
    • Tozkoparan, B., N. Gökhan, G. Aktay, E. Yeşilada, and M. Ertan. 2000. 6-Bezylidenethiazolo[3,2-b]1,2,4-triazole-5(6H)-ones substituted with ibuprofen: synthesis, characterization and evaluation of anti-inflammatory activity. European Journal of Medicinal Chemistry 35: 743-750. (Pubitemid 30490282)
    • (2000) European Journal of Medicinal Chemistry , vol.35 , Issue.7-8 , pp. 743-750
    • Tozkoparan, B.1    Gokhan, N.2    Aktay, G.3    Yesilada, E.4    Ertan, M.5
  • 35
    • 77950866644 scopus 로고    scopus 로고
    • Synthesis and cyclooxygenase inhibitory activities of some N-acylhydrazone derivatives of isoxazolo[4,5-d]pyridazin-4(5H)-ones
    • 20207453 10.1016/j.ejmech.2010.02.012
    • Ünsal-Tan, O., K. Özden, A. Rauk, and A. Balkan. 2010. Synthesis and cyclooxygenase inhibitory activities of some N-acylhydrazone derivatives of isoxazolo[4,5-d]pyridazin-4(5H)-ones. European Journal of Medicinal Chemistry 45: 2345-2352.
    • (2010) European Journal of Medicinal Chemistry , vol.45 , pp. 2345-2352
    • Ünsal-Tan, O.1    Özden, K.2    Rauk, A.3    Balkan, A.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.