Dipartimento di Biologia Evolutiva e Funzionale, Viale GP Usberti 11/A, 43124 Parma, Italy.
Phytochemistry. 2012 Feb;74:159-65. doi: 10.1016/j.phytochem.2011.10.012. Epub 2011 Nov 22.
Some years ago we demonstrated the cytokinin-like activity of the synthetic N-phenyl-N'-benzothiazol-6-ylurea (PBU) and a relevant adventitious rooting adjuvant activity of symmetric urea derivatives devoid of any cytokinin- or auxin-like activity per se. Here we report the synthesis and the biological activity evaluation of nine symmetric or asymmetric ureas/thioureas, structurally related to PBU. None of them show cytokinin-like activity, while we demonstrate for the first time that PBU interacts with Arabidopsis cytokinin receptor CRE1/AHK4 in a heterologous bioassay system. Among the PBU derivatives, all the symmetric ureas/thioureas show an adventitious rooting adjuvant activity in various bioassays, confirming that this activity is strictly dependent on their chemical structure.
数年前,我们证明了合成 N-苯基-N’-苯并噻唑-6-基脲(PBU)具有细胞分裂素样活性,以及对称脲衍生物具有与细胞分裂素或生长素本身无关的不定根形成促进活性。在这里,我们报告了 9 种与 PBU 结构相关的对称或不对称脲/硫脲的合成和生物活性评价。它们都没有表现出细胞分裂素样活性,但我们首次证明 PBU 在异源生物测定系统中与拟南芥细胞分裂素受体 CRE1/AHK4 相互作用。在 PBU 衍生物中,所有的对称脲/硫脲在各种生物测定中都表现出不定根形成促进活性,这证实了这种活性严格依赖于它们的化学结构。