메뉴 건너뛰기




Volumn 24, Issue 4, 2013, Pages 325-328

Synthesis and bioactivities of some new 1H-pyrazole derivatives containing an aryl sulfonate moiety

Author keywords

Anti inflammatory activity; COX 2 inhibitors; Enaminone; p Toluene sulfonyl chloride; Pyrazole

Indexed keywords


EID: 84876688002     PISSN: 10018417     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cclet.2013.02.016     Document Type: Article
Times cited : (17)

References (21)
  • 2
    • 0142165030 scopus 로고    scopus 로고
    • The mechanism of action of aspirin
    • J.R. Vane, and R.M. Botting The mechanism of action of aspirin Thromb. Res. 110 2003 255 258
    • (2003) Thromb. Res. , vol.110 , pp. 255-258
    • Vane, J.R.1    Botting, R.M.2
  • 3
    • 0342561627 scopus 로고    scopus 로고
    • Association between nonsteroidal anti-inflammatory drugs and upper gastrointestinal tract bleeding/perforation
    • S. Hernandez-Diaz, and L.A.G. Rodriguez Association between nonsteroidal anti-inflammatory drugs and upper gastrointestinal tract bleeding/perforation Arch. Intern. Med. 160 2000 2093 2099
    • (2000) Arch. Intern. Med. , vol.160 , pp. 2093-2099
    • Hernandez-Diaz, S.1    Rodriguez, L.A.G.2
  • 4
    • 23844551911 scopus 로고    scopus 로고
    • Selective COX-2 inhibitors and risk of myocardial infarction
    • F. Krotz, T.M. Schiele, and V. Klauss Selective COX-2 inhibitors and risk of myocardial infarction J. Vasc. Res. 42 2005 312 324
    • (2005) J. Vasc. Res. , vol.42 , pp. 312-324
    • Krotz, F.1    Schiele, T.M.2    Klauss, V.3
  • 6
    • 77649295601 scopus 로고    scopus 로고
    • Pyrazole compound BPR1P0034 with potent and selective anti-influenza virus activity
    • S.R. Shih, T.Y. Chu, and G.R. Reddy Pyrazole compound BPR1P0034 with potent and selective anti-influenza virus activity J. Biomed. Sci. 17 2010 13
    • (2010) J. Biomed. Sci. , vol.17 , pp. 13
    • Shih, S.R.1    Chu, T.Y.2    Reddy, G.R.3
  • 7
    • 0011723947 scopus 로고    scopus 로고
    • Synthesis and antitumor activity of novel pyrimidinyl pyrazole derivatives. II. Optimization of the phenylpiperazine moiety of 1-[5-methyl-1-(2-pyrimidinyl)-4-pyrazolyl]-3-phenylpiperazinyl-1-trans-propenes
    • H. Naito, S. Ohsuki, M. Sugimori, and R. Atsumi Synthesis and antitumor activity of novel pyrimidinyl pyrazole derivatives. II. Optimization of the phenylpiperazine moiety of 1-[5-methyl-1-(2-pyrimidinyl)-4-pyrazolyl]-3- phenylpiperazinyl-1-trans-propenes Chem. Pharm. Bull. 50 2002 453 462
    • (2002) Chem. Pharm. Bull. , vol.50 , pp. 453-462
    • Naito, H.1    Ohsuki, S.2    Sugimori, M.3    Atsumi, R.4
  • 8
    • 67650493170 scopus 로고    scopus 로고
    • Synthesis of novel pyrazole derivatives and evaluation of their antidepressant and anticonvulsant activities
    • M. Abdel-Aziz, G.A. Abuo-Rahma, and A.A. Hassan Synthesis of novel pyrazole derivatives and evaluation of their antidepressant and anticonvulsant activities Eur. J. Med. Chem. 44 2009 3480 3487
    • (2009) Eur. J. Med. Chem. , vol.44 , pp. 3480-3487
    • Abdel-Aziz, M.1    Abuo-Rahma, G.A.2    Hassan, A.A.3
  • 9
    • 80053122600 scopus 로고    scopus 로고
    • Synthesis of some novel 1-H pyrazoles derivatives and their antibacterial activity studies
    • P.B.R. Kumar, S. Subramaniyan, K. Yamini, and R. Suthakaran Synthesis of some novel 1-H pyrazoles derivatives and their antibacterial activity studies Russ. J. Chem. 4 2011 400 404
    • (2011) Russ. J. Chem. , vol.4 , pp. 400-404
    • Kumar, P.B.R.1    Subramaniyan, S.2    Yamini, K.3    Suthakaran, R.4
  • 10
    • 80054890054 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of novel pyrazole derivatives with anticancer activity
    • A. Balbi, M. Anzaldi, and C. Macciò Synthesis and biological evaluation of novel pyrazole derivatives with anticancer activity Eur. J. Med. Chem. 46 2011 5293 5309
    • (2011) Eur. J. Med. Chem. , vol.46 , pp. 5293-5309
    • Balbi, A.1    Anzaldi, M.2    Macciò, C.3
  • 11
    • 84555196165 scopus 로고    scopus 로고
    • Synthesis and analgesic activity of some new pyrazoles and triazoles bearing a 6,8-dibromo-2-methylquinazoline moiety
    • H.A. Saad, N.A. Osman, and A.H. Moustafa Synthesis and analgesic activity of some new pyrazoles and triazoles bearing a 6,8-dibromo-2-methylquinazoline moiety Molecules 16 2011 10187 10201
    • (2011) Molecules , vol.16 , pp. 10187-10201
    • Saad, H.A.1    Osman, N.A.2    Moustafa, A.H.3
  • 12
    • 0141884330 scopus 로고    scopus 로고
    • Synthesis of some novel imidazolinones as potent anticonvulsant agents
    • H. Joshi, P. Upadhyay, D. Karia, and A. Baxi Synthesis of some novel imidazolinones as potent anticonvulsant agents Eur. J. Med. Chem. 38 2003 837 840
    • (2003) Eur. J. Med. Chem. , vol.38 , pp. 837-840
    • Joshi, H.1    Upadhyay, P.2    Karia, D.3    Baxi, A.4
  • 13
    • 79953276875 scopus 로고    scopus 로고
    • Studies on synthesis of some novel heterocyclic azlactone derivatives and imidazolinone derivatives and their antimicrobial activity
    • R.N. Mistry, and K.R. Desai Studies on synthesis of some novel heterocyclic azlactone derivatives and imidazolinone derivatives and their antimicrobial activity Eur. J. Chem. 2 2005 42 51
    • (2005) Eur. J. Chem. , vol.2 , pp. 42-51
    • Mistry, R.N.1    Desai, K.R.2
  • 14
    • 0035180107 scopus 로고    scopus 로고
    • Papillomavirus microbicidal activities of high-molecular-weight cellulose sulfate, dextran sulfate, and polystyrene sulfonate
    • N.D. Christensen, C.A. Reed, and T.D. Culp Papillomavirus microbicidal activities of high-molecular-weight cellulose sulfate, dextran sulfate, and polystyrene sulfonate Antimicrob. Agents Chemother. 45 2001 3427 3432
    • (2001) Antimicrob. Agents Chemother. , vol.45 , pp. 3427-3432
    • Christensen, N.D.1    Reed, C.A.2    Culp, T.D.3
  • 15
    • 13344262687 scopus 로고    scopus 로고
    • Naphthalene sulfonate polymers with CD4-blocking and anti-human immunodeficiency virus type 1 activities
    • S. Rusconi, M. Moonis, and D.P. Merrill Naphthalene sulfonate polymers with CD4-blocking and anti-human immunodeficiency virus type 1 activities Antimicrob. Agents Chemother. 40 1996 234 236
    • (1996) Antimicrob. Agents Chemother. , vol.40 , pp. 234-236
    • Rusconi, S.1    Moonis, M.2    Merrill, D.P.3
  • 16
    • 84876669202 scopus 로고
    • Sulfonate ester-containing (imidazol-1-yl)-n-substituted benzene sulfonamides of anticipated antineoplastic activity
    • M.A. Hanna, M.M. Girges, and M.A. Berghot Sulfonate ester-containing (imidazol-1-yl)-n-substituted benzene sulfonamides of anticipated antineoplastic activity Phosphorus Sulfur Silicon Relat. Elem. 61 1991 239 246
    • (1991) Phosphorus Sulfur Silicon Relat. Elem. , vol.61 , pp. 239-246
    • Hanna, M.A.1    Girges, M.M.2    Berghot, M.A.3
  • 17
    • 33646386175 scopus 로고    scopus 로고
    • Ether aryl sulfonic acid esters with improved antimalarial/anticancer activities
    • L.M. Betts, N.C. Tam, S.M.H. Kabir, R.F. Langler, and I. Crandall Ether aryl sulfonic acid esters with improved antimalarial/anticancer activities Aust. J. Chem. 59 2006 277 282
    • (2006) Aust. J. Chem. , vol.59 , pp. 277-282
    • Betts, L.M.1    Tam, N.C.2    Kabir, S.M.H.3    Langler, R.F.4    Crandall, I.5
  • 18
    • 84876676720 scopus 로고    scopus 로고
    • Synthetic approaches and biological evaluation of some new sulfonate ester-containing imidazolone derivatives
    • O.M.O. Habib, H.M. Hassan, E.B. Moawad, and A. El-Mekabaty Synthetic approaches and biological evaluation of some new sulfonate ester-containing imidazolone derivatives Am. J. Org. Chem. 2 2012 79 86
    • (2012) Am. J. Org. Chem. , vol.2 , pp. 79-86
    • Habib, O.M.O.1    Hassan, H.M.2    Moawad, E.B.3    El-Mekabaty, A.4
  • 19
    • 24944541510 scopus 로고    scopus 로고
    • Iodine and iodic acid: An efficient reagent combination for iodination of aryl hydroxy ketones
    • B.R. Patil, S.R. Bhusare, R.P. Pawar, and Y.B. Vibhute Iodine and iodic acid: an efficient reagent combination for iodination of aryl hydroxy ketones Tetrahedron Lett. 46 2005 7179 7181
    • (2005) Tetrahedron Lett. , vol.46 , pp. 7179-7181
    • Patil, B.R.1    Bhusare, S.R.2    Pawar, R.P.3    Vibhute, Y.B.4
  • 20
    • 0038579439 scopus 로고    scopus 로고
    • Pyridinium bromochromate: A new and efficient reagent for bromination of hydroxy aromatics
    • S.B. Patwari, M.A. Baseer, Y.B. Vibhute, and S.R. Bhusare Pyridinium bromochromate: a new and efficient reagent for bromination of hydroxy aromatics Tetrahedron Lett. 44 2003 4893 4894
    • (2003) Tetrahedron Lett. , vol.44 , pp. 4893-4894
    • Patwari, S.B.1    Baseer, M.A.2    Vibhute, Y.B.3    Bhusare, S.R.4
  • 21
    • 84876677150 scopus 로고    scopus 로고
    • Indian Pharmacopoeia Publication & Information Directorate India
    • Indian Pharmacopoeia Microbiological Assays and Tests vol. 2 1996 Publication & Information Directorate India pp. A-100-A-116
    • (1996) Microbiological Assays and Tests , vol.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.