ANTI-INFLAMMATORY AND ANTICANCER AGENT WITH HYDRONAPHTHALENE DERIVATIVE AS ACTIVE INGREDIENT, AND NEW HYDRONAPHTHALENE DERIVATIVE

PROBLEM TO BE SOLVED: To obtain the subject new compound having an activity to inhibit production of O2 by human neutrophil, activity to inhibit growth of the mouse's lymphatic leukemia cell P388, and an anti-inflammatory and anticancer action. SOLUTION: This hydronaphthalene derivative is show...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: SHINOHARA TSUTOMU, KAMIMURA DAISUKE, KURAMOTO MAKOTO, YAZAWA KAZUYOSHI, ARIMOTO HIROICHI, SHINOHARA YUIKO, KANO MAYUMI, YAMADA KAORU
Format: Patent
Sprache:eng
Schlagworte:
Online-Zugang:Volltext bestellen
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:PROBLEM TO BE SOLVED: To obtain the subject new compound having an activity to inhibit production of O2 by human neutrophil, activity to inhibit growth of the mouse's lymphatic leukemia cell P388, and an anti-inflammatory and anticancer action. SOLUTION: This hydronaphthalene derivative is shown by formula I or II (R is OH, a lower akoxy or NR R ; R and R are each H or a C-C double bond chain; R , R and R are each H or a lower alkyl; R and R are each H, OH, a lower alkoxy or C-C double bond chain; R is H, OH or a lower alkoxy; R and R are each H or a lower alkyl), e.g. [2E,4E]-5-(5',6',7',8'- tetrahydro-1'-naphthyl)-2,4-pentadienoic acid. The compound shown by formula I is obtained from Penicillium citrinum SCRC-SA124 cultivated under an aerobic condition by organic solvent extraction or chromatographic separation of the cultivated bacterium or the supernatant of the medium. The compound shown by formula II is obtained by the chemical synthesis in which 5,6,7,8-tetrahydro-1- naphthyltrifluoromethanesulfonate is reacted with ethyl [2E,4E]-5- tributylstannyl-2,4-pentadienoate or the like.