GRADE & PURITYMoligand™?Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools.≥98%(HPLC)
Zeatin upon reduction forms zeatin O-glucoside, which is widely present in plants. It possesses transportation and storage functions, along with defence against zeatin oxidases.
trans-Zeatin is a plant cytokinin
Condiciones de almacenamiento de almacenamiento
Store at -20°C, Argon charged
Enviado en
Ice chest + Ice pads
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Grado
Moligand™
Nota
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
This compound belongs to the class of organic compounds known as 6-alkylaminopurines. These are compounds that contain an alkylamine group attached at the 6-position of a purine. Purine is a bicyclic aromatic compound made up of a pyrimidine ring fused to an imidazole ring.
External Descriptors
zeatin
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
1.Zan Li, Jun Jia, Mingwei Wang, Hua Zhang, Hongyuan Yan, Fengxia Qiao. (2017) Bifunctionalized ordered mesoporous organosilica synthesized in deep eutectic solvent for extraction of triazine herbicides from watermelon. JOURNAL OF CHROMATOGRAPHY A, [PMID:29132822][10.1016/j.chroma.2017.10.074]
2.Yong-Lan Ma, Min Li, Qian Lei, Hai-Jun Ma, Ya-Jing An. (2025) Trans-Zeatin Enhances Auxenochlorella pyrenoidosa Growth by Coordinating Carbon–Nitrogen Metabolism and Antioxidant Defense. Microorganisms, 13 (11):(2554). [PMID:41304239][10.3390/microorganisms13112554]
Calculadoras de soluciones
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Reseñas
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