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Volumn 12, Issue 5, 2004, Pages 1239-1255

Synthesis and biological evaluation of novel macrocyclic bis-7-azaindolylmaleimides as potent and highly selective glycogen synthase kinase-3β (GSK-3β) inhibitors

Author keywords

Azaindolemaleimide; Coupling; Cross x11dummy; Kinase; Specific inhibitor

Indexed keywords

6,7,8,13,14,15 HEXAHYDRO 9,12 EPITHIO 5,25:16,21 DIMETHENODIPYRIDO[2,3 B:3',2' H]PYRROLO[3,4 E][1,10]DIAZACYCLOTRICOSINE 22,24(23H) DIONE; 7 AZAINDOLYLMALEIMIDE DERIVATIVE; 7,8,9,10,11,12,13,14 OCTAHYDRO 10 HYDROXY 6H,21H 5,24:15,20 DIMETHENODIPYRIDO[2,3 B:3',2' H]PYRROLO[3,4 E][1,10]DIAZACYCLONONADECINE 21,23(22H) DIONE; 7,8,9,11,12,13,14 HEPTAHYDRO 6H,21H 5,24:15,20 DIMETHENODIPYRIDO[2,3 B:3',2' H]PYRROLO[3,4 E][1,10]DIAZACYCLONONADECINE 10,21,23(22H) TRIONE; AZAINDOLYLMALEIMIDE DERIVATIVE; CROWN ETHER DERIVATIVE; CYCLIN DEPENDENT KINASE 2; ENZYME INHIBITOR; GLYCOGEN SYNTHASE KINASE 3BETA INHIBITOR; MACROCYCLIC COMPOUND; MALEIMIDE DERIVATIVE; NITROGEN; OXYGEN; PALLADIUM; PROTEIN KINASE; PROTEIN KINASE C BETA; THIOPHENE; UNCLASSIFIED DRUG;

EID: 10744228214     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmc.2003.09.047     Document Type: Article
Times cited : (33)

References (53)
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    • Recently, it was reported that condensation of a 7-azaindole Grignard reagent with the less readily available 3,4-dibromo-N-methylmaleimide gave bis-7-azaindolylmaleimide:
    • Recently, it was reported that condensation of a 7-azaindole Grignard reagent with the less readily available 3,4-dibromo-N-methylmaleimide gave bis-7-azaindolylmaleimide: Routier S., Ayerbe N., Me'rour J.-Y., Coudert G., Bailly C., Pierr'e A., Pfeiffer B., Caignard D.-H., Renard P. Tetrahedron. 58:2002;6621.
    • (2002) Tetrahedron , vol.58 , pp. 6621
    • Routier, S.1    Ayerbe, N.2    Me'Rour, J.-Y.3    Coudert, G.4    Bailly, C.5    Pierr'E, A.6    Pfeiffer, B.7    Caignard, D.-H.8    Renard, P.9
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    • It was reported that the removal of N-2,4-dimethoxybenzyl protecting group in maleimides could be achieved by using TFA/anisole/90°C condition in some cases but failed in other cases
    • It was reported that the removal of N-2,4-dimethoxybenzyl protecting group in maleimides could be achieved by using TFA/anisole/90°C condition in some cases but failed in other cases Watson D.J., Dowdy E.D., Li W.-S., Wang J., Polniaszek R. Tetrahedron Lett. 42:2001;1827.
    • (2001) Tetrahedron Lett. , vol.42 , pp. 1827
    • Watson, D.J.1    Dowdy, E.D.2    Li, W.-S.3    Wang, J.4    Polniaszek, R.5
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    • note
    • The kinetic studies that demonstrated compound 46 and polyoxygenated bis-7-azaindolylmaleimide are ATP competitive inhibitors will be published in a separate manuscript.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.