Description
A member of the class of 6-aminopurines that is adenine in which one of the hydrogens of the amino group is replaced by a benzyl group.
Chemical properties
| Chemical formula | Net charge | Average mass |
|---|---|---|
| C12H11N5 | 0 | 225.24944 |
Nomenclature
| IUPAC | SMILES | InChI | InChIKey | Synonyms |
|---|---|---|---|---|
| N-benzyl-9H-purin-6-amine | C(Nc1ncnc2[nH]cnc12)c1ccccc1 | InChI=1S/C12H11N5/c1-2-4-9(5-3-1)6-13-11-10-12(15-7-14-10)17-8-16-11/h1-5,7-8H,6H2,(H2,13,14,15,16,17) | NWBJYWHLCVSVIJ-UHFFFAOYSA-N |
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Citations
- Montalbán, IA, et al. 2012. Endogenous cytokinin and auxin profiles during in vitro organogenesis from vegetative buds of Pinus radiata adult trees. Physiologia Plantarum. 148(2).
- Perán, R, et al. 2006. Cryopreservation, encapsulation and promotion of shoot production of embryonic axes of a recalcitrant species Ekebergia capensis, Sparrm. Cryo Letters. 27(1).
- Verma, S, et al. 2014. A novel combination of plant growth regulators for in vitro regeneration of complete plantlets of guar [Cyamopsis tetragonoloba (L.) Taub]. Indian Journal of Experimental Biology. 51(12).