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Cyasterone

Table 2< Effects of fl-ecdysone as compared to cyasterone and ponasterone A when orally Injected to 4th Instar B, mopi, 25 larvae were used per treatment. Table 2< Effects of fl-ecdysone as compared to cyasterone and ponasterone A when orally Injected to 4th Instar B, mopi, 25 larvae were used per treatment.
Oral Injections >10 jig of fl-ecdysone also resulted In a promoted apolysls, but depending upon concentration and the exact age of the treated fourth Instar larvae, a variable number of the treated larvae were able to complete molting and essentially recover. Cyasterone Injections >10 yg, In general, caused a delay (antl-ecdysone) of molting of the treated fourth Instar larvae to the fifth Instar. This antlecdysone effect of cyasterone, at Its most severe, resulted In prothetely (precocious development) of a small % of the treated larvae. [Pg.337]

From Table 7 it can be seen that ajugasterone C is more than 10-fold more potent than 8-ecdysone, and more than 30-fold more potent than cyasterone, as a feeding deterrent to S- grcaninum when Incorporated into the artlflcal diet of this behavioral bio-assay. [Pg.344]

Trillium camschatcense Ker-Gawler Yan Ling Cao (root) Trillin, trillarin, diosgenin, cyasterone, ecdysterone.48 Improve blood circultation, detoxicant, treat headache, high blood pressure, stop bleeding. [Pg.165]

Ecdysones cyasterone Ajuga bracteosa, A. decumbens, A. pygmaea... [Pg.419]

Cyasterone (sterol) Ajuga charrmepitys, A. nipponensis, ECDY-R agonist... [Pg.462]

Ecdysone Itself and the phytoecdysones, inokosterone and maklsterone A, were much less effective as abortifacients than 20-0HE (Table I). Cyasterone and ponasterone A were inactive the implication being that the hydroxyl group on C25 is required for activity (10). [Pg.410]

Figure 6.11 Structure and sites of biochemical modification of phytoecdysteroids. The structures of the most commonly reported phytoecdysteroid, 20-hydroxyecdysone, and a 24-alkylphytoecdysteroid, cyasterone. Some common sites of biochemical modifications reported for phytoecdysteroids. (From Adler and Grebenok, 1999.)... Figure 6.11 Structure and sites of biochemical modification of phytoecdysteroids. The structures of the most commonly reported phytoecdysteroid, 20-hydroxyecdysone, and a 24-alkylphytoecdysteroid, cyasterone. Some common sites of biochemical modifications reported for phytoecdysteroids. (From Adler and Grebenok, 1999.)...
Sarcophaga bioassav ponasterone A 2p-glucoside (29) sengosterone (36) pterosterone (38) stachysterone C (39) capitasterone (43) cyasterone (48) amarasterone A (51) amarasterone B (52) ajugasterone C (53) rubrosterone (72)... [Pg.28]


See other pages where Cyasterone is mentioned: [Pg.333]    [Pg.333]    [Pg.334]    [Pg.335]    [Pg.345]    [Pg.23]    [Pg.244]    [Pg.411]    [Pg.59]    [Pg.65]    [Pg.80]    [Pg.11]    [Pg.13]    [Pg.27]    [Pg.28]    [Pg.30]    [Pg.31]    [Pg.34]    [Pg.42]    [Pg.60]    [Pg.61]    [Pg.207]    [Pg.688]    [Pg.412]    [Pg.406]    [Pg.213]    [Pg.27]    [Pg.30]    [Pg.31]   
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See also in sourсe #XX -- [ Pg.27 ]

See also in sourсe #XX -- [ Pg.231 , Pg.526 ]

See also in sourсe #XX -- [ Pg.286 ]




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Cell-free assays cyasterone activity

Cyasterones

Cyasterones

Cyasterones activity

Ecdysones cyasterone

Musca bioassay cyasterone activity

Phytoecdysteroids cyasterone

Sarcophaga bioassay cyasterone activity

Whole insect assays cyasterone activity

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