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Inhibitory role of gibberellins in theobroxide-induced flowering of Pharbitis nil

✍ Scribed by Xiquan Gao; Fanjiang Kong; Fang Wang; Hideyuki Matsuura; Teruhiko Yoshihara

Book ID: 116690066
Publisher: Elsevier Science
Year: 2006
Tongue: English
Weight: 344 KB
Volume: 163
Category: Article
ISSN: 0176-1617
DOI: 10.1016/j.jplph.2005.04.028

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On the treatment with acetic anhydride-pyridine at room temparature the four glucosldes gave the ccrresponding acetates. Chemical shifts in the NMR spectra of the glucosides and their acetates are summarized in Table. Esterification of a crystalline F-II tetraacetate (II), Cj~H40015H20\*\*, m.p. 20

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We have isolated seven gibberellin glucosides (1, 2) from immature seeds of morning-glory (Pharbitis nil) and elucidated the structures of six of them - (3). Now we wish to report the structure of a new gibberellin glucoside, tentatively termed F-VII.

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Structures of gibberellins A26 and A27 in immature seeds of pharbitis nil

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Isolation and. biological activities of new gibberellins A26 and A27 in immature seeds of the Japanese morning-glory (Pharbitis nil) have been reported - (1). We wish to report here the elucidation of their structures. Gibberellin A26 (GA26), m.p. 254-257", formed a monomethyl ester (II), m.p. 207