Biological activity of 3-formylchromones and related compound

In Vivo

Volumn 21, Issue 5, 2007, Pages 829-834

  Kawase, Masami ^a   Tanaka, Toru ^b   Kan, Hiroyuki ^b   Tani, Satoru ^b   Nakashima, Hideki ^c   Sakagami, Hiroshi ^d  

^a MATSUYAMA UNIVERSITY   (Japan)

^b JOSAI UNIVERSITY   (Japan)

^c ST MARIANNA UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^d MEIKAI UNIVERSITY SCHOOL OF DENTISTRY   (Japan)

Author keywords

3 Formylchromone; Anti Helicobacter pylori; Anti HIV; Cytotoxic activity; Urease

Indexed keywords

3 ACETYLCOUMARIN; 3 CYANOCHROMONE; 3 FORMYL 6 ISOPROPYLCHROMONE; 3 FORMYL 6 METHYLCHROMONE; 3 FORMYL 6 NITROCHROMONE; 3 FORMYLCHROMONE; 3 FORMYLCHROMONE DERIVATIVE; 6 BROMO 3 FORMYLCHROMONE; 6 CHLORO 3 FORMYL 7 METHYLCHROMONE; 6 CHLORO 3 FORMYLCHROMONE; 6 FLUORO 3 FORMYLCHROMONE; 6 METHOXY 3 FORMYLCHROMONE; 6,8 DIBROMO 3 FORMYLCHROMONE; 6,8 DICHLORO 3 FORMYLCHROMONE; ANTIINFECTIVE AGENT; ANTINEOPLASTIC AGENT; ANTIVIRUS AGENT; CHROMONE; CHROMONE DERIVATIVE; CLARITHROMYCIN; COUMARIN 3 CARBOXYLIC ACID; COUMARIN 3 CARBOXYLIC ACID ETHYL ESTER; COUMARIN DERIVATIVE; CURDLAN; DEXTRAN SULFATE; DOXORUBICIN; EPIGALLOCATECHIN GALLATE; METRONIDAZOLE; UNCLASSIFIED DRUG; UNINDEXED DRUG; ZIDOVUDINE;

ANTIBACTERIAL ACTIVITY; ANTIVIRAL ACTIVITY; ARTICLE; CANCER CELL CULTURE; CHEMICAL MODIFICATION; CONTROLLED STUDY; DRUG CYTOTOXICITY; DRUG POTENCY; DRUG STRUCTURE; DRUG SYNTHESIS; ENZYME INHIBITION; HELICOBACTER PYLORI; HUMAN; HUMAN CELL; HUMAN IMMUNODEFICIENCY VIRUS; NONHUMAN; STRUCTURE ACTIVITY RELATION;

EID: 35648973169     PISSN: 0258851X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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