Benzo[c][2,7]naphthyridines from 2,6-dinor-nifedipine and its dimethyl 2,5-dicarboxylate isomer;Benzo[c][2,7]naphthyridine aus 2,6-dinor-nifedipin und dessen 2,5-dicarbonsäuredimethylester-isomer

Pharmazie

Volumn 59, Issue 1, 2004, Pages 15-20

  Gorlitzer K ^a,b   Bode, M ^a   Frohberg, P ^b   Drutkowski, G ^b  

^a MARTIN LUTHER UNIVERSITY HALLE WITTENBERG   (Germany)

^b TECHNICAL UNIVERSITY OF BRAUNSCHWEIG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

1,4 DIHYDROPYRIDINE; 15 HYDROXYICOSATETRAENOIC ACID; 2 NITROBENZALDEHYDE; 2,6 DINORNIFEDIPINE; ARACHIDONATE 5 LIPOXYGENASE; BENZALDEHYDE DERIVATIVE; BENZO[C][2,7]NAPHTHYRIDINE; CHLORIDE; HYDROXAMIC ACID; NAPHTHYRIDINE DERIVATIVE; NIFEDIPINE; PHOSPHORUS; PLATINUM; PROSTAGLANDIN SYNTHASE; UNCLASSIFIED DRUG; ZILEUTON; ZINC;

ANTIMALARIAL ACTIVITY; ARTICLE; CYCLIZATION; DEHYDROGENATION; DIFFERENTIAL PULSE VOLTAMMETRY; DRUG SYNTHESIS; ENZYME INHIBITION; ISOMER; OXIDATION; PH; ULTRAVIOLET A RADIATION;

ANTIMALARIALS; ARACHIDONATE 5-LIPOXYGENASE; ARACHIDONIC ACID; CYCLIZATION; ELECTROCHEMISTRY; HUMANS; HYDROCHLORIC ACID; HYDROXAMIC ACIDS; HYDROXYEICOSATETRAENOIC ACIDS; INDICATORS AND REAGENTS; ISOMERISM; LIPOXYGENASE INHIBITORS; NAPHTHYRIDINES; NIFEDIPINE; OXIDATION-REDUCTION; ULTRAVIOLET RAYS; ZINC;

EID: 17044448884     PISSN: 00317144     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (10)

1. Carbateas PM, Williams GL (1974) Two methods for conversion of an aromatic aldehyde to a 4-arylpyridine. A method for preparation of 3-alkyl-4-arylpyridines. J Heterocycl Chem 11: 819-821.
2. Chennat T, Eisner U (1975) A new synthesis of 1,4-dihydropyridines. J Chem Soc Perkin Trans 1: 926-929.
3. Clemens F, Drutkowski G, Wiese M, Frohberg P (2001) The inactivation of lipoxygenase-1 from soybeans by amidrazones. Biochim Biophys Acta 1549: 88-98.
4. Funk CD (2001) Prostaglandins and leukotrienes: advances in eicosanoid biology. Science 294: 1871-1875.
5. Görlitzer K, Dobberkau P-M, Jones PG (1996) Fünfring-Analoga von Nifedipin. 2. Mitteilung: Zur Photochemie von 2,6-Dimethyl-1,4-dihydropyridin-3,5-dicarbonsäure-dimethylestern mit 4-(2-Nitro-3-furyl)- und 4-(2-Nitro-3-thienyl)-Substituenten. Pharmazie 51: 392-396.
6. Görlitzer K, Fabian J, Jones PG, Frohberg P, Drutkowski G (2002a) Furo[2,3-c]chinoline und Furo[3,4-c]chinoline - Synthese und Prüfung auf Lipoxygenase-Hemmung. Pharmazie 57: 159-168.
7. Görlitzer K, Fabian J, Jones PG, Frohberg P, Drutkowski G (2002b) Pyridazino[3,4-c]chinoline und Pyridazino[4,5-c]chinoline - Synthese und Prüfung auf Lipoxygenase-Hemmung. Pharmazie 57: 362-371.
8. Ludvik J, Volke J, Pragst F (1986) Investigation of two radical intermediates in the anodic oxidation of 1,4-dihydropyridines by electrochemiluminescence. J Electroanal Chem 215: 179-190.
9. Ludvik J, Volke J, Klima J (1987) Electrochemical oxidation mechanisms of different type 1,4-dihydropyridine derivatives in acetonitrile. Electrochim Acta 32: 1063-1071.
10. Skala V, Volke J, Ohanka V, Kuthan J (1977) On dihydropyridines XXXV. Electrochemical oxidation of 3,5-difunctional 1,4-dihydropyridine derivatives. Collect Czech Chem Commun 42: 292-305.