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kw.\*:("PYRAZOLO (3,4-B) PYRAZINE")

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GLYCOSIDES DU PYRAZOLE ET DES SYSTEMES PYRAZOLIQUES CONDENSES HETEROCYCLIQUES. XIV. SYNTHESE DES N-OXYDES DE PYRAZOLO (3,4-B) PYRAZINE ET DE SON RIBOSIDEKORBUKH IA; YAKUNINA NG; DORN KH et al.1976; ZH. ANORG. KHIM.; S.S.S.R.; DA. 1976; VOL. 12; NO 4; PP. 900-903; BIBL. 8 REF.Article

ETUDE DE LA STRUCTURE DES INDAZOLES, DES PYRAZOLO (3,4-B) PYRIDINES ET DE LA PYRAZOLO (3,4-B) PYRAZINE PAR SPECTROSCOPIE IRSENNITSKAYA LV; TIMOSHENKOVA YU D; KIKOT BS et al.1977; KHIM. GETEROCIKL. SOEDIN.; S.S.S.R.; DA. 1977; NO 5; PP. 662-667; BIBL. 17 REF.Article

Facile synthesis of some new pyrazolo[3,4-b] pyrazines and their antifungal activityEL-EMARY, T. I; KAMAL EL-DEAN, A. M; EL-KASHEF, H. S et al.Il Farmaco (Pavia). 1998, Vol 53, Num 6, pp 383-388, issn 0014-827XArticle

A New Cyclization to Fused Pyrazoles Tunable for Pericyclic or Pseudopericyclic Route : An Experimental and Theoretical StudyFILAK, Laszlo; ROKOB, Tibor Andras; VASKO, Gyöngyvér Agnes et al.Journal of organic chemistry. 2008, Vol 73, Num 10, pp 3900-3906, issn 0022-3263, 7 p.Article

2,3,5-Trisubstituted pyridines as selective AKT inhibitors. Part II: Improved drug-like properties and kinase selectivity from azaindazolesHONG LIN; YAMASHITA, Dennis S; ZHIHONG LAI et al.Bioorganic & medicinal chemistry letters (Print). 2010, Vol 20, Num 2, pp 679-683, issn 0960-894X, 5 p.Article

New pyrazolo[3,4-b]pyrazines : synthesis and biological activityEL-KASHEF, H. S; EL-EMARY, T. I; GASQUET, M et al.Pharmazie. 2000, Vol 55, Num 8, pp 572-576, issn 0031-7144Article

ALLGEMEINE SYNTHESEN UND RATIONELLE STRUKTURPARAMETER ISOMERER DERIVATE VON (3,4)-KONDENSIERTEN PYRAZOLEN = SYNTHESES GENERALES ET PARAMETRES STRUCTURAUX DE DERIVES ISOMERES DE PYRAZOLES CONDENSES EN (3,4)DORN H; OZEGOWSKI R.1979; J. PRAKT. CHEM.; DDR; DA. 1979; VOL. 321; NO 6; PP. 881-898; ABS. ENG; BIBL. 32 REF.Article

Pyrazoloheteroaryls : Novel p38α MAP kinase inhibiting scaffolds with oral activityREVESZ, Laszlo; BLUM, Ernst; DI PADOVA, Franco E et al.Bioorganic & medicinal chemistry letters (Print). 2006, Vol 16, Num 2, pp 262-266, issn 0960-894X, 5 p.Article

Tetrasubstituted pyridines as potent and selective AKT inhibitors: Reduced CYP450 and hERG inhibition of aminopyridinesHONG LIN; YAMASHITA, Dennis S; VENSLAVSKY, Joseph et al.Bioorganic & medicinal chemistry letters (Print). 2010, Vol 20, Num 2, pp 684-688, issn 0960-894X, 5 p.Article

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