Description
A 6-alkylaminopurine that is 7H-purin-6-amine where one of the hydrogens of the amino group is replaced by a 4-hydroxy-3-methylbutyl group. It is an intermediate in the zeatin biosynthesis.
Chemical properties
| Chemical formula | Net charge | Average mass |
|---|---|---|
| C10H15N5O | 0 | 221.25900 |
Nomenclature
| IUPAC | SMILES | InChI | InChIKey | Synonyms |
|---|---|---|---|---|
| (2R)-2-methyl-4-(7H-purin-6-ylamino)butan-1-ol | C[C@@H](CO)CCNc1ncnc2nc[nH]c12 | InChI=1S/C10H15N5O/c1-7(4-16)2-3-11-9-8-10(13-5-12-8)15-6-14-9/h5-7,16H,2-4H2,1H3,(H2,11,12,13,14,15)/t7-/m1/s1 | XXFACTAYGKKOQB-SSDOTTSWSA-N |
|
Citations
- Abul, Y, et al. 2010. Occurrence of plant growth regulators in Psilotum nudum. Journal of Plant Physiology. 167(14).
- Bromley, JR, et al. 2013. A purine nucleoside phosphorylase in Solanum tuberosum L. (potato) with specificity for cytokinins contributes to the duration of tuber endodormancy. The Biochemical Journal. 458(2).
- Hayashi, K, et al. 2012. Design and synthesis of photolabile caged cytokinin. Bioorganic & Medicinal Chemistry Letters. 22(17).