Description
A 9-ribosylzeatin having cis-zeatin as the nucleobase.
Chemical properties
| Chemical formula | Net charge | Average mass |
|---|---|---|
| C15H21N5O5 | 0 | 351.35770 |
Nomenclature
| IUPAC | SMILES | InChI | InChIKey | Synonyms |
|---|---|---|---|---|
| N-[(2Z)-4-hydroxy-3-methylbut-2-en-1-yl]adenosine | C\C(CO)=C\CNc1ncnc2n(cnc12)[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O | InChI=1S/C15H21N5O5/c1-8(4-21)2-3-16-13-10-14(18-6-17-13)20(7-19-10)15-12(24)11(23)9(5-22)25-15/h2,6-7,9,11-12,15,21-24H,3-5H2,1H3,(H,16,17,18)/b8-2-/t9-,11-,12-,15-/m1/s1 | GOSWTRUMMSCNCW-BAJUWZQUSA-N |
|
Citations
- Banowetz, GM, et al. 1993. Monoclonal antibodies against the plant cytokinin, cis-zeatin riboside. Hybridoma. 12(6).
- Mauk, CS, et al. 1978. Physiology of Tuberization in Solanum tuberosum L: cis-Zeatin Riboside in the Potato Plant: Its Identification and Changes in Endogenous Levels as Influenced by Temperature and Photoperiod. Plant Physiology. 62(3).
- McCloskey, JA, et al. 1980. Occurrence and levels of cis-and trans-zeatin ribosides in the culture medium of a virulent strain of Agrobacterium tumefaciens. FEBS Letters. 111(1).