메뉴 건너뛰기




Volumn 5, Issue 8, 2014, Pages 878-883

Identification of novel phenyl butenonyl C-glycosides with ureidyl and sulfonamidyl moieties as antimalarial agents

Author keywords

Antimalarial agent; diarylureides; phenyl sulfonamides; Plasmodium falciparum

Indexed keywords

AMINOPHENYL GLYCOSYL PYRANOSIDE; ANTIMALARIAL AGENT; GLYCOPYRANOSIDE; GLYCOSIDE; SULFONAMIDE; THIOUREIDO GLUCOSIDE; UNCLASSIFIED DRUG; UREIDO GLUCOSIDE;

EID: 84906262237     PISSN: None     EISSN: 19485875     Source Type: Journal    
DOI: 10.1021/ml500211c     Document Type: Article
Times cited : (16)

References (29)
  • 1
    • 84906246539 scopus 로고    scopus 로고
    • World Health Organization: Geneva, Switzerland.
    • WHO Malarial Report 2013; World Health Organization: Geneva, Switzerland, 2013.
    • (2013) WHO Malarial Report 2013
  • 2
    • 0031752556 scopus 로고    scopus 로고
    • Drug Resistance in Malaria
    • White, N. J. Drug Resistance in Malaria Br. Med. Bull. 1998, 54, 703-715
    • (1998) Br. Med. Bull. , vol.54 , pp. 703-715
    • White, N.J.1
  • 6
    • 0034864129 scopus 로고    scopus 로고
    • New Class of Small Nonpeptidyl Compounds Blocks Plasmodium falciparum Development in Vitro by Inhibiting Plasmepsins
    • Jiang, S.; Prigge, S. T.; Wei, L.; Gao, Y.; Hudson, T. H.; Gerena, L.; Dame, J. B.; Kyle, D. E. New Class of Small Nonpeptidyl Compounds Blocks Plasmodium falciparum Development In Vitro by Inhibiting Plasmepsins Antimicrob. Agents Chemother. 2001, 45, 2577-2584
    • (2001) Antimicrob. Agents Chemother. , vol.45 , pp. 2577-2584
    • Jiang, S.1    Prigge, S.T.2    Wei, L.3    Gao, Y.4    Hudson, T.H.5    Gerena, L.6    Dame, J.B.7    Kyle, D.E.8
  • 11
    • 0037934729 scopus 로고    scopus 로고
    • Validation of the Hexose Transporter of Plasmodium falciparum as a Novel Drug Target
    • Joet, T.; Eckstein-Ludwig, U.; Morin, C.; Krishna, S. Validation of the Hexose Transporter of Plasmodium falciparum as a Novel Drug Target Proc. Natl. Acad. Sci. U.S.A. 2003, 100, 7476-7479
    • (2003) Proc. Natl. Acad. Sci. U.S.A. , vol.100 , pp. 7476-7479
    • Joet, T.1    Eckstein-Ludwig, U.2    Morin, C.3    Krishna, S.4
  • 13
    • 77949357436 scopus 로고    scopus 로고
    • Life Cycle Studies of the Hexose Transporter of Plasmodium Species and Genetic Validation of Their Essentiality
    • Slavic, K.; Straschil, U.; Reininger, L.; Doerig, C.; Morin, C.; Tewari, R.; Krishna, S. Life Cycle Studies of the Hexose Transporter of Plasmodium Species and Genetic Validation of Their Essentiality Mol. Microbiol. 2010, 75, 1402-1413
    • (2010) Mol. Microbiol. , vol.75 , pp. 1402-1413
    • Slavic, K.1    Straschil, U.2    Reininger, L.3    Doerig, C.4    Morin, C.5    Tewari, R.6    Krishna, S.7
  • 15
    • 0035818913 scopus 로고    scopus 로고
    • Antimalarial Alkoxylated and Hydroxylated Chalones: Structure-Activity Relationship Analysis
    • Liu, M.; Wilairat, P.; Go, M. L. Antimalarial Alkoxylated and Hydroxylated Chalones: Structure-Activity Relationship Analysis J. Med. Chem. 2001, 44, 4443-4452
    • (2001) J. Med. Chem. , vol.44 , pp. 4443-4452
    • Liu, M.1    Wilairat, P.2    Go, M.L.3
  • 16
    • 4344668584 scopus 로고    scopus 로고
    • Antiplasmodial Chalcones Inhibit Sorbitol-Induced Hemolysis of Plasmodium falciparum -Infected Erythrocytes
    • Go, M. L.; Liu, M.; Wilairat, P.; Rosenthal, P. J.; Saliba, K. J.; Kirk, K. Antiplasmodial Chalcones Inhibit Sorbitol-Induced Hemolysis of Plasmodium falciparum -Infected Erythrocytes Antimicrob. Agents Chemother. 2004, 48, 3241-3245
    • (2004) Antimicrob. Agents Chemother. , vol.48 , pp. 3241-3245
    • Go, M.L.1    Liu, M.2    Wilairat, P.3    Rosenthal, P.J.4    Saliba, K.J.5    Kirk, K.6
  • 19
    • 0038548308 scopus 로고    scopus 로고
    • Structure-Activity Relationships of Antileishmanial and Antimalarial Chalcones
    • Liu, M.; Wilairat, P.; Croft, S. L.; Tan, A. L.; Go, M. L. Structure-Activity Relationships of Antileishmanial and Antimalarial Chalcones Bioorg. Med. Chem. 2003, 11, 2729-2738
    • (2003) Bioorg. Med. Chem. , vol.11 , pp. 2729-2738
    • Liu, M.1    Wilairat, P.2    Croft, S.L.3    Tan, A.L.4    Go, M.L.5
  • 20
    • 38049156628 scopus 로고    scopus 로고
    • In Vitro Antimalarial Activity of Flavonoids and Chalcones
    • Lim, S. S.; Kim, H. S.; Lee, D. U. In Vitro Antimalarial Activity of Flavonoids and Chalcones Bull. Korean Chem. Soc. 2007, 28, 2495-2497
    • (2007) Bull. Korean Chem. Soc. , vol.28 , pp. 2495-2497
    • Lim, S.S.1    Kim, H.S.2    Lee, D.U.3
  • 21
    • 77957832893 scopus 로고    scopus 로고
    • Reinvestigation of Structure-Activity Relationship of Methoxylated Chalcones As Antimalarials: Synthesis and Evaluation of 2,4,5-Trimethoxy Substituted Patterns As Lead Candidates Derived from Abundantly Available Natural β-Asarone
    • Kumar, R.; Mohanakrishnan, D.; Sharma, A.; Kaushik, N. K.; Kalia, K.; Sinha, A. K.; Sahal, D. Reinvestigation of Structure-Activity Relationship of Methoxylated Chalcones As Antimalarials: Synthesis and Evaluation of 2,4,5-Trimethoxy Substituted Patterns As Lead Candidates Derived from Abundantly Available Natural β-Asarone Eur. J. Med. Chem. 2010, 45, 5292-5301
    • (2010) Eur. J. Med. Chem. , vol.45 , pp. 5292-5301
    • Kumar, R.1    Mohanakrishnan, D.2    Sharma, A.3    Kaushik, N.K.4    Kalia, K.5    Sinha, A.K.6    Sahal, D.7
  • 22
    • 45849124658 scopus 로고    scopus 로고
    • Synthesis of Novel Substituted 1,3-Diaryl Propenone Derivatives and Their Antimalarial Activity in Vitro
    • Mishra, N.; Arora, P.; Kumar, B.; Mishra, L. C.; Bhattacharya, A.; Awasthi, S. K.; Bhasin, V. K. Synthesis of Novel Substituted 1,3-Diaryl Propenone Derivatives and Their Antimalarial Activity in Vitro Eur. J. Med. Chem. 2008, 43, 1530-1535
    • (2008) Eur. J. Med. Chem. , vol.43 , pp. 1530-1535
    • Mishra, N.1    Arora, P.2    Kumar, B.3    Mishra, L.C.4    Bhattacharya, A.5    Awasthi, S.K.6    Bhasin, V.K.7
  • 23
    • 84866361218 scopus 로고    scopus 로고
    • release version 4.1; Accelrys Inc. San Diego, CA.
    • Catalyst, release version 4.1; Accelrys Inc.: San Diego, CA, 2006.
    • (2006) Catalyst
  • 24
    • 0034699895 scopus 로고    scopus 로고
    • A Convenient, One-Step, synthesis of β- C -Glycosidic Ketones in Aqueous Media
    • Rodrigues, F.; Canac, Y.; Lubineau, A. A Convenient, One-Step, synthesis of β- C -Glycosidic Ketones in Aqueous Media Chem. Commun. 2000, 2049-2050
    • (2000) Chem. Commun. , pp. 2049-2050
    • Rodrigues, F.1    Canac, Y.2    Lubineau, A.3
  • 25
    • 0036303578 scopus 로고    scopus 로고
    • C -Glycosides by Aqueous Condensation of β-Dicarbonyl Compounds with Unprotected Sugars
    • Riemann, I.; Papadopoulos, M. A.; Knorst, M.; Fessner, W. D. C -Glycosides by Aqueous Condensation of β-Dicarbonyl Compounds with Unprotected Sugars Aust. J. Chem. 2002, 55, 147-154
    • (2002) Aust. J. Chem. , vol.55 , pp. 147-154
    • Riemann, I.1    Papadopoulos, M.A.2    Knorst, M.3    Fessner, W.D.4
  • 26
    • 65549105906 scopus 로고    scopus 로고
    • A Novel and Efficient Direct Aldol Condensation from Ketones and Aromatic Aldehydes Catalyzed by Proline-TEA through a New Pathway
    • Wang, J. F.; Lei, M.; Li, Q.; Ge, Z.; Wang, X.; Li, R. A Novel and Efficient Direct Aldol Condensation from Ketones and Aromatic Aldehydes Catalyzed by Proline-TEA through a New Pathway Tetrahedron 2009, 65, 4826-4833
    • (2009) Tetrahedron , vol.65 , pp. 4826-4833
    • Wang, J.F.1    Lei, M.2    Li, Q.3    Ge, Z.4    Wang, X.5    Li, R.6
  • 27
    • 44249113269 scopus 로고    scopus 로고
    • Aldol Reaction of β- C -Glycosylic Ketones: Synthesis of C -(E)-Cinnamoyl Glycosylic Compounds as Precursors for New Biologically Active C -Glycosides
    • Bisht, S. S.; Pandey, J.; Sharma, A.; Tripathi, R. P. Aldol Reaction of β- C -Glycosylic Ketones: Synthesis of C -(E)-Cinnamoyl Glycosylic Compounds as Precursors for New Biologically Active C -Glycosides Carbohydr. Res. 2008, 343, 1399-1406
    • (2008) Carbohydr. Res. , vol.343 , pp. 1399-1406
    • Bisht, S.S.1    Pandey, J.2    Sharma, A.3    Tripathi, R.P.4
  • 28
    • 84869823388 scopus 로고    scopus 로고
    • Chemoselective Synthesis of Polyfunctional Aminophenyl 2-Oxobut-3-enyl- and Quinolinylmethyl- C- glycopyranosides from Nitrophenyl 2-Oxobut-3-enyl C -Glycopyranosides under Ultrasonic Vibration
    • Ramakrishna, K. K. G.; Ajay, A.; Sharma, A.; Tripathi, R. P. Chemoselective Synthesis of Polyfunctional Aminophenyl 2-Oxobut-3-enyl- and Quinolinylmethyl- C- glycopyranosides from Nitrophenyl 2-Oxobut-3-enyl C -Glycopyranosides under Ultrasonic Vibration Arkivoc 2013, ii, 146-165
    • (2013) Arkivoc , vol.2 , pp. 146-165
    • Ramakrishna, K.K.G.1    Ajay, A.2    Sharma, A.3    Tripathi, R.P.4
  • 29
    • 0027275566 scopus 로고
    • Physiological Parameters in Laboratory Animals and Humans
    • Davies, B.; Morris, T. Physiological Parameters in Laboratory Animals and Humans Pharm. Res. 1993, 10, 1093-1095
    • (1993) Pharm. Res. , vol.10 , pp. 1093-1095
    • Davies, B.1    Morris, T.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.