trans-Zeatin

For research use only. Not for therapeutic Use.

  • CAT Number: R013637
  • CAS Number: 1637-39-4
  • Molecular Formula: C10H13N5O
  • Molecular Weight: 219.248
  • Purity: ≥95%
Inquiry Now

<p>
<span style=/line-height:1.5;/>trans-Zeatin is a member of the plant hormone family known as ‘cytokinins’, which regulate cell division, development, and nutrient processing.&nbsp;</span>
</p>
<p>
<span style=/line-height:1.5;/>The biosynthesis of cytokinins involves isoprenylation of ATP or ADP, with trans-Zeatin being produced by the removal of phosphate and riboside groups from adenine and oxidation by cytochrome P735A. trans-Zeatin evokes its effects through high affinity receptors, including Arabidopsis histidine kinases (AHK). The affinity of trans-zeatin for AHK3, which is important in mediating plant development, has been reported to be 1.3 nM.</span>
</p>
<p>
<span style=/line-height:1.5;/><br />
</span>
</p>
<p>
<span style=/line-height:1.5;/><b>Application / Uses</b><span style=/color:#333333;font-family:Arial, serif;font-size:13px;line-height:20.8px;background-color:#FFFFFF;/>&nbsp;</span><br />
</span>
</p>
<ul style=/color:#333333;font-family:Arial, serif;font-size:13px;/>
<li>
Promotes callus initiation when combined with auxin, concentration 1 ppm.
</li>
<li>
Promotes fruit set. Zeatin 100 ppm + GA3 500 ppm + NAA 20 ppm, sprayed at 10th, 25th, 40th day after blossom.
</li>
<li>
Retards yellowing for vegetables, 20 ppm, sprayed.
</li>
<li>
Causes auxiliary stems to grow and flower.
</li>
<li>
It can also be applied to stimulate seed germination and seedling growth.
</li>
</ul>
<br />
<p>
<br />
</p>


Catalog Number R013637
CAS Number 1637-39-4
Synonyms

(2E)-2-Methyl-4-(9H-purin-6-ylamino)-2-buten-1-ol; 6-(4-Hydroxy-3-methyl?-trans-2-butenylamino)purine; N6-(4-Hydroxy-3-methyl-trans-2-butenyl)adenine; ZT; ZTA; Zeatin; (E)-Zeatin; Zeatine;

Molecular Formula C10H13N5O
Purity ≥95%
Target Stem Cell/Wnt
Solubility H2O: soluble
Storage -20°C
IUPAC Name (E)-2-methyl-4-(7H-purin-6-ylamino)but-2-en-1-ol
InChI 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+
InChIKey UZKQTCBAMSWPJD-FARCUNLSSA-N
SMILES CC(=CCNC1=NC=NC2=C1NC=N2)CO
Reference

<p>
[1].&nbsp;To, J.P.C., and Kieber, J.J. Cytokinin signaling: Two-components and more. Trends in Plant Science 13(2), 85-92 (2008).
</p>
<p>
[2].&nbsp;Hirose, N.,Takei, K.,Kuroha, T., et al. Regulation of cytokinin biosynthesis, compartmentalization and translocation. Journal of Experimental Botany 59(1), 75-83 (2008).
</p>
<p>
[3].&nbsp;Veit, B. Hormone mediated regulation of the shoot apical meristem. Plant Molecular Biology 69, 397-408 (2009).
</p>
<p>
<span><br />
</span>
</p>
<p>
<span></span>
</p>

Request a Quote