Synthesis and antitumor activity of some 5H-pyrrolizine, pyrimido [5,4-a] pyrrolizine pyrimido[4,5-b]pyrrolizine derivatives

Saudi Pharmaceutical Journal

Volumn 17, Issue 1, 2009, Pages 3-18

  Aly, Samir M El Moghazy ^a   Mohamed, Mohamed A Azim ^a   Farag, Awatif El S ^a   Gouda, Ahmed M ^b  

^a CAIRO UNIVERSITY   (Egypt)

^b Beni Suef University   (Egypt)

Author keywords

Anticancer; Probit analysis; Pyrimido 4,5 b pyrrolizine; Pyrimido 5,4 a pyrrolizine; Pyrrolizine

Indexed keywords

1 CYANO 2 (3 ETHYLUREIDO) 3N PHENYL 6,7 DIHYDRO 5H PYRROLIZINE 3 CARBOXAMIDE; 1 CYANO 2 (3 PHENYLUREIDO) 3N PHENYL 6,7 DIHYDRO 5H PYRROLIZINE 3 CARBOXAMIDE; 1 CYANO 2 (3 SUBSTITUTED UREIDO) 3N PHENYL 6,7 DIHYDRO PYRROLIZINE 3 CARBOXAMIDE; 1 CYANO 2 [3 (4 CHLOROPHENYL)UREIDO] 3N TOLYL 6,7 DIHYDRO 5H PYRROLIZINE 3 CARBOXAMIDE; 2 AMINO 1 CYANO 6,7 DIHYDRO 5H PYRROLIZINE 3 CARBOXAMIDE; 2 AMINO 3N (4 METHYLPHENYL) 6,7 DIHYDRO 5H PYRROLIZINE 1,3 DICARBOXAMIDE; 2 AMINO 3N PHENYL 6,7 DIHYDRO 5H PYRROLIZINE 1,3 DICARBOXAMIDE; 2,4 DIOXO 1H PYRIMIDO[4,5 B]PYRROLIZINE 9 CARBONITRILE; 2,4 DIOXO 3 (4 METHOXYPHENYL) 2,3,4,6,7,8 HEXAHYDRO 1H PYRIMIDO[4,5 B]PYRROLIZINE 9 CARBONITRILE; 2,4 DIOXO 3 PHENYL 2,3,4,6,7,8 HEXAYDRO 1H PYRIMIDO[4,5 B]PYRROLIZINE 9 CARBONITRILE; 2,4 DIOXO 3 TOLYL 2,3,4,6,7,8 HEXAYDRO 1H PYRIMIDO[4,5 B]PYRROLIZINE 9 CARBONITRILE; 3 (4 CHLOROPHENYL) 4 IMINO 2 OXO 9N (4 CHLOROPHENYL) 2,3,4,5,6,7 HEXAHYDRO 1H PYRIMIDO[5,4 A]PYRROLIZINE 9 CARBOXAMIDE; 3 (4 CHLOROPHENYL) 4 IMINO 2 OXO 9N PHENYL 2,3,4,5,6,7 HEXAHYDRO 1H PYRIMIDO[5,4 A]PYRROLIZINE 9 CARBOXAMIDE; 3 (ALKYLPHENYL) 4 IMINO 2 OXO 9N PHENYL 2,3,4,5,6,7 HEXAHYDRO 1 H PYRIMIDO[5,4 A]PYRROLIZINE 9 CARBOXAMIDE; 3 ETHYL 4 IMINO 2 OXO 9N PHENYL 2,3,4,5,6,7 HEXAHYDRO 1H PYRIMIDO[5,4 A]PYRROLIZINE 9 CARBOXAMIDE; 3 PHENYL 4 IMINO 2 OXO 9N PHENYL 2,3,4,5,6,7 HEXAHYDRO 1H PYRIMIDO[5,4 A]PYRROLIZINE 9 CARBOXAMIDE; 4 AMINO 3 (4 CHLOROPHENYL) 2 OXO 9N (4 CHLOROPHENYL) 2,3,4,5,6,7 HEXAHYDRO 1H PYRIMIDO[5,4 A]PYRROLIZINE 9 CARBOXAMIDE; 4 AMINO 3 (4 CHLOROPHENYL) 2 OXO 9N (4 METHYLPHENYL) 2,3,4,5,6,7 HEXAHYDRO 1H PYRIMIDO[5,4 A]PYRROLIZINE 9 CARBOXAMIDE; 4 AMINO 3 (4 CHLOROPHENYL) 2 OXO 9N PHENYL 2,3,4,5,6,7 HEXAHYDRO 1H PYRIMIDO[5,4 A]PYRROLIZINE 9 CARBOXAMIDE; 4 AMINO 3 ETHYL 2 OXO 9N (4 METHOXYPHENYL) 2,3,4,5,6,7 HEXAHYDRO 1H PYRIMIDO[5,4 A]PYRROLIZINE 9 CARBOXAMIDE; 4 AMINO 3 ETHYL 2 OXO 9N PHENYL 2,3,4,5,6,7 HEXAHYDRO 1H PYRIMIDO[5,4 A]PYRROLIZINE 9 CARBOXAMIDE; 4 OXO 9N (4 METHYLPHENYL) 4,5,6,7 TETRAHYDRO 3H PYRIMIDO[5,4 A]PYRROLIZINE 9 CARBOXAMIDE; 4 OXO 9N PHENYL 4,5,6,7 TETRAHYDRO 3H PYRIMIDO[5,4 A]PYRROLIZINE 9 CARBOXAMIDE; ANTINEOPLASTIC AGENT; ETHYL (1 CYANO 3 PHENYLCARBAMOYL 6,7 DIHYDRO 5H PYRROLIZIN 2 YL CARBAMATE); ETHYL [1 CYANO 3 (4 TOLYLCARBAMOYL 6,7 DIHYDRO 5H PYRROLIZIN 2 YL CARBAMATE)]; PYRIMIDO[4,5 B]PYRROLIZINE DERIVATIVE; PYRIMIDO[5,4 A]PYRROLIZINE DERIVATIVE; PYRROLIZINE DERIVATIVE; UNCLASSIFIED DRUG; UNINDEXED DRUG;

ANTINEOPLASTIC ACTIVITY; ARTICLE; CANCER INHIBITION; CONCENTRATION RESPONSE; CONTROLLED STUDY; DRUG SCREENING; DRUG STRUCTURE; DRUG SYNTHESIS; HUMAN; HUMAN CELL; IN VITRO STUDY; MICROANALYSIS; MOLECULAR WEIGHT; STRUCTURE ANALYSIS;

EID: 61849132369     PISSN: 13190164     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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