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Senkyunolide

The volatiles showed variation in different environments. The composition of the oil from the fresh aerial parts of A. graveolensvai. secalinum (at the flowering stage) obtained from three locations in Egypt revealed that the main components were a- and /3-pinene, myrcene, limonene, cis-jl- ocimene, y-terpinene, cis-allo-ocimene, frans-farnesene, humulene, apiol, /3-selinene, senkyunolide and neocnidilide (Saleh et al., 1985). The chief component in the essential oils from fruits, and to a lesser extent in the leaves and stems, was limonene, whereas the roots and tubers had more frans-ocimene, 3-methyl-... [Pg.402]

Senkyunolide B (3Z-Butylidene-7- hydroxyphthalide) 93236-67-0 Angelica sinensis Cnidium officinale Ligusticum chuanxiong, L. wallichii Meum athamanticum [4, 9, 20, 24, 25]... [Pg.618]

Senkyunolide D 94530-82-2 Angelica sinensis Cnidium officinale Ligusticum wallichii [20, 25, 104]... [Pg.618]

Senkyunolide E 94530-83-3 or Angelica acutiloba, A. sinensis Cnidium officinale Ligusticum [4, 5, 20, 21,... [Pg.618]

Senkyunolide G (3-Butyl-4,5-dihydro-3- hydroxyphthalide) 94530-85-5 Angelica sinensis Cnidium officinale Ligusticum sinense c.v. chaxiong, L. wallichii [20, 25, 103, 104]... [Pg.618]

Senkyunolide M (3Z-Butylidene-4,5,6,7-tetrahydro-75-hyd roxy-67 -(l-oxobutyl)phthalide) 114569-34-5 Angelica acutiloba Ligusticum chuanxiong, L. wallichii [20, 108, 109]... [Pg.619]

Senkyunolide N (35-Butyl-4,5,6,7-tetrahydro-6S,7S -dihydroxyphthalide) 140694-58-2 Apiurn graveolens Ligusticum chuanxiong [9, 107]... [Pg.619]

Senkyunolide Q (3Z-Butyl idene-4,5,6,7-tetrahydro-7/ -hydroxy-6 R-( 1 -oxobutyl)phthalide) 142235-81-2 Ligusticum chuanxiong [109]... [Pg.619]

Senkyunolide R (3Z-Butylidene-4,5,6,7-te trahydro-27 ,65,75-trihydroxyphthalide) 172549-37-0 Ligusticum chuanxiong [110]... [Pg.619]

Anti-platelet aggregation and anti-thrombosis Butylidenephthalide (20), 3/ -Butylphthalide (31), 3S-Butylphthalide (32), Z-Ligustilide (49), Senkyunolide A (58)... [Pg.638]

Blood viscosity reduction Butylphthalide (30), Cnidilide (41), Senkyunolide A (58), Senkyunolide P (115), Levistolide B (117)... [Pg.638]

Naito et al. investigated reduction of blood viscosity by nine phthalides [301]. Among the compounds tested, two phthalide dimers tokinolide B (118) and senkyunolide P (116), and three 3-substituted phthalides butylphthalide (30), cnidilide (41) and senkyunolide A (58), significantly reduced blood viscosity in Wistar rats. The blood viscosity reduction was 7.3%, 9.4%, 9.4%, 18.5% and 12.8% for phthalides 30, 41, 58, 115 and 117, respectively. The other four phthalides 20, 47, 111 and 113 did not significantly affect blood viscosity. [Pg.642]

Other phthalides have also been investigated for their effects on cardiac function. Ligustilide (47) and senkyunolide A (58) exerted negative inotropic actions without changing atrial contraction rate in the isolated guinea pig atria [306]. [Pg.643]

The vasodilatory actions of various phthalide dimers were studied in several isolated rat preparations [301], While they did not alter methoxamine-induced perfusion pressure of mesenteric arteries, the phthalide dimers relaxed KCl-induced vasoconstriction in rat aorta with decreasing potency according to the following order tokinolide B (117) > levistolide A (111) > senkyunolide P (115) > riligustilide (113) [301]. Subsequently these four phthalide dimers were claimed in a Japanese patent to produce vasodilatory effects on KC1 and noradrenaline contracted rat mesenteric arteries [146]. [Pg.651]

See other pages where Senkyunolide is mentioned: [Pg.406]    [Pg.618]    [Pg.618]    [Pg.622]    [Pg.622]    [Pg.638]    [Pg.641]    [Pg.642]    [Pg.643]    [Pg.643]    [Pg.644]    [Pg.645]    [Pg.645]    [Pg.645]    [Pg.645]    [Pg.645]    [Pg.652]    [Pg.653]    [Pg.654]    [Pg.654]    [Pg.654]    [Pg.890]    [Pg.497]   
See also in sourсe #XX -- [ Pg.402 , Pg.406 ]

See also in sourсe #XX -- [ Pg.638 ]

See also in sourсe #XX -- [ Pg.165 ]

See also in sourсe #XX -- [ Pg.165 , Pg.428 , Pg.670 ]



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