Description
The trans-isomer of zeatin.
Chemical properties
| Chemical formula | Net charge | Average mass |
|---|---|---|
| C10H13N5O | 0 | 219.24332 |
Nomenclature
| IUPAC | SMILES | InChI | InChIKey | Synonyms |
|---|---|---|---|---|
| (2E)-2-methyl-4-(9H-purin-6-ylamino)but-2-en-1-ol | C\C(CO)=C/CNc1ncnc2[nH]cnc12 | InChI=1S/C10H13N5O/c1-7(4-16)2-3-11-9-8-10(13-5-12-8)15-6-14-9/h2,5-6,16H,3-4H2,1H3,(H2,11,12,13,14,15)/b7-2+ | UZKQTCBAMSWPJD-FARCUNLSSA-N |
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Citations
- Bujacz, GD, et al. 2003. Crystallization and preliminary crystallographic studies of mung bean cytokinin-specific binding protein. Acta Crystallographica. Section D, Biological Crystallography. 59(Pt 3).
- Großkinsky, DK, et al. 2013. Cis- and trans-zeatin differentially modulate plant immunity. Plant Signaling & Behavior. 8(7).
- Sasaki, E, et al. 2013. Uniconazole, a cytochrome P450 inhibitor, inhibits trans-zeatin biosynthesis in Arabidopsis. Phytochemistry. 87.