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Volumn 45, Issue 2, 2010, Pages 805-810

Synthesis and preliminary biological evaluation of new derivatives of the marine alkaloid leucettamine B as kinase inhibitors

Author keywords

Kinase inhibitors; Leucettamine B; Marine alkaloid; Microwave irradiation; Reductive amination; Solvent free; Sulfur nitrogen displacement

Indexed keywords

5 [(1,3 BENZODIOXO 5 YL)METHYLENE] 3 METHYL 2 [(2 (Z) BENZYLIDENEAMINO)ETHYLAMINO] 3,5 DIHYDRO 4H IMIDAZOL 4 ONE; 5 [(1,3 BENZODIOXO 5 YL)METHYLENE] 3 METHYL 2 [(2 (Z)(1,3 BENZODIOXOL 5 YL)METHYLENEAMINO]ETHYLAMINO] 3,5 DIHYDRO 4H IMIDAZOL 4 ONE; 5 [(1,3 BENZODIOXO 5 YL)METHYLENE] 3 METHYL 2 [2 (Z)(4 NITROBENZYLIDENEAMINO)ETHYLAMINO] 3,5 DIHYDRO 4H IMIDAZOL 4 ONE; 5 [(1,3 BENZODIOXO 5 YL)METHYLENE] 3 METHYL 2 [2(Z)(3,4,5 TRIMETHOXYBENZYLIDENEAMINO)ETHYLAMINO] 3,5 DIHYDRO 4H IMIDAZOL 4 ONE; 5 [(1,3 BENZODIOXO 5 YL)METHYLENE] 3 METHYL 2 [2(Z)(4 CHLOROBENZYLIDENEAMINO)ETHYLAMINO] 3,5 DIHYDRO 4H IMIDAZOL 4 ONE; 5 [(1,3 BENZODIOXO 5 YL)METHYLENE] 3 METHYL 2 [2(Z)(4 METHOXYBENZYLIDENEAMINO)ETHYLAMINO] 3,5 DIHYDRO 4H IMIDAZO 4 ONE; 5 [(1,3 BENZODIOXO 5 YL)METHYLENE] 3 METHYL 2 [[2 (Z)(2,3 DIHYDROBENZO[1,4]DIOXIN 6 YL)METHYLENEAMINO]ETHYLAMINO] 3,5 DIHYDRO 4H IMIDAAZOL 4 ONE; 5 [(1,3 BENZODIOXO 5 YL)METHYLENE] 3 METHYL 2 [[2 (Z)(2,3 DIHYDROFURAN 5 YL)METHYLENEAMINO)ETHYLAMINO] 3,5 DIHYDRO 4H IMIDAZOL 4 ONE; 5 BENZO[1,3] DIOXO 5 YLMETHYLENE 2 ETHYLSULFANYL 3,5 DIHYDROIMIDAZOL 4 ONE; ALKALOID DERIVATIVE; CASEIN KINASE IALPHA; CYCLIN DEPENDENT KINASE 5; ETHYLENEDIAMINE; GLYCOGEN SYNTHASE KINASE 3ALPHA; GLYCOGEN SYNTHASE KINASE 3BETA; IMIDAZOLE DERIVATIVE; LEUCETTAMINE B; LEUCETTAMINE B DERIVATIVE; NITROGEN; PROTEIN KINASE INHIBITOR; SULFUR; UNCLASSIFIED DRUG;

EID: 73849133993     PISSN: 02235234     EISSN: 17683254     Source Type: Journal    
DOI: 10.1016/j.ejmech.2009.10.009     Document Type: Article
Times cited : (38)

References (16)
  • 6
    • 36649022638 scopus 로고    scopus 로고
    • (5Z) 5-[(1,3-benzodioxo-5-yl)methylene]-3-methyl-2-ethylsulfanyl-3,5-dihydroi midazol-4-one 3 is prepared stereoselectively by one-pot three component domino reaction, see:
    • (5Z) 5-[(1,3-benzodioxo-5-yl)methylene]-3-methyl-2-ethylsulfanyl-3,5-dihydroi midazol-4-one 3 is prepared stereoselectively by one-pot three component domino reaction, see:. Renault S., Bertrand S., Carreaux F., and Bazureau J.P. J. Comb. Chem. 9 (2007) 935-942
    • (2007) J. Comb. Chem. , vol.9 , pp. 935-942
    • Renault, S.1    Bertrand, S.2    Carreaux, F.3    Bazureau, J.P.4
  • 8
    • 73849125683 scopus 로고    scopus 로고
    • note
    • The guanylation step can be performed under thermal process but requires a large excess of amine (solvent) and a long reaction time (>24 h) which complicates the purification of the final product.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.