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Volumn 23, Issue 2, 2014, Pages 759-764

Synthesis and biological evaluation of benzo[d]imidazolyl chromeno[2,3-d]pyrimidinones

Author keywords

Anti bacterial activity; Anti fungal activity; Anti oxidant activity; Benzo d imidazolyl chromeno 2,3 d pyrimidinones; Condensation

Indexed keywords

2 CYANO N (2 MERCAPTO 1H BENZO[DEXTRO]IMIDAZOL 5 YL)ACETAMIDE; 2 IMINO N (2 MERCAPTO 1H BENZO[DEXTRO]IMIDAZOL 5 YL) 2H CHROMENE 3 CARBOXAMIDE; 2 IMINO N (2 MERCAPTO 1H BENZO[DEXTRO]IMIDAZOL 5 YL) 7 METHOXY 2H CHROMENE 3 CARBOXAMIDE; 3 (2 MERCAPTO 1H BENZO[DEXTRO]IMIDAZOL 5 YL) 2H CHROMENO[2,3 DEXTRO]PYRIMIDIN 4 (3H)ONE; 3 (2 MERCAPTO 1H BENZO[DEXTRO]IMIDAZOL 5 YL) 8 METHOXY 2H CHROMENO[2,3 DEXTRO]PYRIMIDIN 4 (3H)ONE; 5 AMINO 2 MERCAPTOBENZIMIDAZOLE; 7 BROMO 2 IMINO N (2 MERCAPTO 1H BENZO[DEXTRO]IMIDAZOL 5 YL) 2H CHROMENE 3 CARBOXAMIDE; 7,8 DIBROMO 2 IMINO N (2 MERCAPTO 1H BENZO[DEXTRO]IMIDAZOL 5 YL) 2H CHROMENE 3 CARBOXAMIDE; 8 BROMO 3 (2 MERCAPTO 1H BENZO[DEXTRO]IMIDAZOL 5 YL) 2H CHROMENO[2,3 DEXTRO]PYRIMIDIN 4 (3H)ONE; 8 CHLORO 3 (2 MERCAPTO 1H BENZO[DEXTRO]IMIDAZOL 5 YL) 2H CHROMENO[2,3 DEXTRO]PYRIMIDIN 4 (3H)ONE; 8,9 DIBROMO 3 (2 MERCAPTO 1H BENZO[DEXTRO]IMIDAZOL 5 YL) 2H CHROMENO[2,3 DEXTRO]PYRIMIDIN 4 (3H)ONE; ANTIINFECTIVE AGENT; ANTIOXIDANT; BENZO[DEXTRO]IMIDAZOLYL CHROMENO[2,3 DEXTRO]PYRIMIDNONE DERIVATIVE; ETHYL CYANOACETATE; PYRIMIDINONE DERIVATIVE; SALICYLALDEHYDE; UNCLASSIFIED DRUG;

EID: 84893804470     PISSN: 10542523     EISSN: 15548120     Source Type: Journal    
DOI: 10.1007/s00044-013-0674-5     Document Type: Article
Times cited : (13)

References (20)
  • 1
    • 35548943623 scopus 로고    scopus 로고
    • Synthesis and molluscicidal activity of new chromene and pyrano[2,3-c]pyrazole derivatives
    • 1:CAS:528:DC%2BD2sXht1KqsLfL 10.1002/ardp.200700157
    • Abdelrazek FM, Metz P, Kataeva O, Jager A, El-Mahrouky SF (2007) Synthesis and molluscicidal activity of new chromene and pyrano[2,3-c]pyrazole derivatives. Arch Pharm 340:543
    • (2007) Arch Pharm , vol.340 , pp. 543
    • Abdelrazek, F.M.1    Metz, P.2    Kataeva, O.3    Jager, A.4    El-Mahrouky, S.F.5
  • 2
    • 15944389028 scopus 로고    scopus 로고
    • Simple coumarins and analogues in medicinal chemistry: Occurrence, synthesis and biological activity
    • 1:CAS:528:DC%2BD2MXjtVCjsb4%3D 15853704 10.2174/0929867053507315
    • Borges F, Roleira F, Milhazes N, Santana L, Uriarte E (2005) Simple coumarins and analogues in medicinal chemistry: occurrence, synthesis and biological activity. Curr Med Chem 12:887
    • (2005) Curr Med Chem , vol.12 , pp. 887
    • Borges, F.1    Roleira, F.2    Milhazes, N.3    Santana, L.4    Uriarte, E.5
  • 3
    • 0000338765 scopus 로고
    • Katritzky AR, Ress CW (eds) Pergamon, Oxford
    • Brown D (1984) In: Katritzky AR, Ress CW (eds) Comprehensive heterocyclic chemistry, vol 3, Pergamon, Oxford, p 443
    • (1984) Comprehensive Heterocyclic Chemistry , vol.3 , pp. 443
    • Brown, D.1
  • 4
    • 33645470355 scopus 로고    scopus 로고
    • Chemistry and biological activity of natural and synthetic prenyloxycoumarins
    • 1:CAS:528:DC%2BD28XisVShsg%3D%3D 16472213 10.2174/092986706775197890
    • Curini M, Cravotto G, Epifano F, Giannone G (2006) Chemistry and biological activity of natural and synthetic prenyloxycoumarins. Curr Med Chem 13:199
    • (2006) Curr Med Chem , vol.13 , pp. 199
    • Curini, M.1    Cravotto, G.2    Epifano, F.3    Giannone, G.4
  • 5
    • 30344447512 scopus 로고    scopus 로고
    • Synthesis and biological activity of some novel thieno[2,3-b]quinoline, quinolino[3′,2′:4,5] thieno[3,2-d]pyrimidine and pyrido[2′,3′:4,5]thieno[2,3-b]quinoline derivatives
    • 1:CAS:528:DC%2BD28XmslSq 10.1080/104265090970322
    • El-Gaby MSA, Abdel-Gawad SM, Ghorab MM, Heiba HI, Aly HM (2006) Synthesis and biological activity of some novel thieno[2,3-b]quinoline, quinolino[3′,2′:4,5] thieno[3,2-d]pyrimidine and pyrido[2′,3′:4,5]thieno[2,3-b]quinoline derivatives. Phosphorus Sulfur Silicon 181:279
    • (2006) Phosphorus Sulfur Silicon , vol.181 , pp. 279
    • El-Gaby, M.S.A.1    Abdel-Gawad, S.M.2    Ghorab, M.M.3    Heiba, H.I.4    Aly, H.M.5
  • 6
    • 0029059734 scopus 로고
    • Synthesis of polysubstituted o-phenylenediamines and their conversion into heterocycles, particularly 2-substituted benzimidazoles with known or potential anthelminthic activity
    • 1:CAS:528:DyaK2MXotlKls7c%3D 10.1016/0040-4020(95)00642-L
    • Hazelton JC, lldon B, Suschitzky H, Wolley LH (1995) Synthesis of polysubstituted o-phenylenediamines and their conversion into heterocycles, particularly 2-substituted benzimidazoles with known or potential anthelminthic activity. Tetrahedron 51:10771
    • (1995) Tetrahedron , vol.51 , pp. 10771
    • Hazelton, J.C.1    Lldon, B.2    Suschitzky, H.3    Wolley, L.H.4
  • 8
    • 0020042950 scopus 로고
    • Pharmacological studies of a new non-steroidal anti-inflammatory drug: 2-(5-ethylpyridin-2-yl)benzimidazole
    • 1:CAS:528:DyaL38XhtFGlt78%3D
    • Ito H, Kagaya T, Fukuda K, Nose T (1982) Pharmacological studies of a new non-steroidal anti-inflammatory drug: 2-(5-ethylpyridin-2-yl)benzimidazole. Arzneim Forsch 32:49
    • (1982) Arzneim Forsch , vol.32 , pp. 49
    • Ito, H.1    Kagaya, T.2    Fukuda, K.3    Nose, T.4
  • 12
    • 33645235480 scopus 로고
    • National Committee for Clinical Laboratory Standards (NCCLS) Nat. Comm. Clini. Lab stands, Ltd. Villanova
    • National Committee for Clinical Laboratory Standards (NCCLS) (1982) Method for dilution antimicrobial susceptibility tests for bacteria, which grows aerobically. National Committee for Clinical Laboratory Standards, Ltd., Villanova, p 242
    • (1982) Method for Dilution Antimicrobial Susceptibility Tests for Bacteria, Which Grows Aerobically , pp. 242
  • 15
    • 77955106843 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of N1-[(3Z)-5-substituted-2-oxo-1,2- dihydro-3H-indol-3-ylidene]-5H-dibenzo[b, f]azepine-5-carbo hydrazides
    • 1:CAS:528:DC%2BC3cXmsVKjtL8%3D 10.3923/ijbc.2010.19.26
    • Ranjit K, Rao GK, Pai PNS (2010) Synthesis and biological evaluation of N1-[(3Z)-5-substituted-2-oxo-1,2-dihydro-3H-indol-3-ylidene]-5H-dibenzo[b, f]azepine-5-carbo hydrazides. Int J Biol Chem 4:19
    • (2010) Int J Biol Chem , vol.4 , pp. 19
    • Ranjit, K.1    Rao, G.K.2    Pai, P.N.S.3
  • 16
    • 1842866611 scopus 로고    scopus 로고
    • Synthesis and anti-HIV activity of 1-(2,6-difluorophenyl)-1H,3H- thiazolo[3,4-a]benzimidazolestructurally-related 1,2-substituted benzimidazoles
    • 1:CAS:528:DC%2BD38XptVOqtrk%3D 12420877 10.1016/S0014-827X(02)01300-9
    • Rao A, Chimirri E, Montorte C (2002) Synthesis and anti-HIV activity of 1-(2,6-difluorophenyl)-1H,3H-thiazolo[3,4-a]benzimidazolestructurally-related 1,2-substituted benzimidazoles. Il Farmaco 57:819
    • (2002) Il Farmaco , vol.57 , pp. 819
    • Rao, A.1    Chimirri, E.2    Montorte, C.3
  • 17
    • 84863821999 scopus 로고    scopus 로고
    • Synthesis, antimicrobial, anti-inflammatory and antioxidant activity of novel Spiro (imidazo[4′,5′:4,5′]benzo[1,2-e][1,4] thiazepine)-9,3′-indolines
    • Ravindernath A, Srinivas Reddy M (2012) Synthesis, antimicrobial, anti-inflammatory and antioxidant activity of novel Spiro (imidazo[4′, 5′:4,5′]benzo[1,2-e][1,4] thiazepine)-9,3′-indolines. J Sulfur Chem 3:363
    • (2012) J Sulfur Chem , vol.3 , pp. 363
    • Ravindernath, A.1    Srinivas Reddy, M.2
  • 18
    • 16044365071 scopus 로고    scopus 로고
    • A synthetic entry into fused pyran derivatives through carbon transfer reactions of 1,3-oxazinanes and oxazolidines with carbon nucleophiles
    • 1:CAS:528:DyaK28XmslyjtL8%3D 10.1016/0040-4020(96)00879-4
    • Singh K, Singh J, Singh H (1996) A synthetic entry into fused pyran derivatives through carbon transfer reactions of 1,3-oxazinanes and oxazolidines with carbon nucleophiles. Tetrahedron 52:14273
    • (1996) Tetrahedron , vol.52 , pp. 14273
    • Singh, K.1    Singh, J.2    Singh, H.3
  • 19
    • 0036809043 scopus 로고    scopus 로고
    • Anti-inflammatory, analgesic and antiamoebic activity evaluation of pyrimido[1,6-a] benzimidazole derivatives synthesized by the reaction of keto isothiocyanates with mono and diamines
    • 1:CAS:528:DC%2BD38Xosl2itLc%3D 12446042 10.1016/S0223-5234(02)01403-4
    • Sondhi SM, Rajvanshi S, Johar M, Bharti N, Azam A, Singh AK (2002) Anti-inflammatory, analgesic and antiamoebic activity evaluation of pyrimido[1,6-a] benzimidazole derivatives synthesized by the reaction of keto isothiocyanates with mono and diamines. Eur J Med Chem 37:835
    • (2002) Eur J Med Chem , vol.37 , pp. 835
    • Sondhi, S.M.1    Rajvanshi, S.2    Johar, M.3    Bharti, N.4    Azam, A.5    Singh, A.K.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.