What is the trans-Zeatin-riboside?

trans-Zeatin-riboside is white to off-white crystalline powder, while it's Molecular Formula is C15H21N5O5. white to off-white crystalline powder trans-Zeatin-riboside is used in tissue culture systems include control of shoot growth and formation, cell division and inhibition of leaf senescence. Cytokinins promote cell division, stimulate shoot proliferation, inhibit root formation, slow the aging process, and activate gene expression and metabolic activity in general.

What is the CAS number for trans-Zeatin-riboside?

The CAS number of trans-Zeatin-riboside is 6025-53-2.

What is trans-Zeatin-riboside (6025-53-2) used for?

Trans-Zeatin-riboside is a naturally occurring plant hormone belonging to the cytokinin class. It is a 9-ribosylzeatin with trans-zeatin as the nucleobase. trans-Zeatin-riboside plays a crucial role in various aspects of plant growth and development, including cell division, shoot proliferation, and the inhibition of leaf senescence.InChI:InChI=1/C15H21N5O5/c1-8(5-21)2-3-16-14-11-9(4-18-19-14)20(7-17-11)15-13(24)12(23)10(6-22)25-15/h2,4,7,10,12-13,15,21-24H,3,5-6H2,1H3,(H,16,19)/t10-,12+,13+,15+/m1/s1

What is the trans-Zeatin-riboside?

trans-Zeatin-riboside is white to off-white crystalline powder, while it's Molecular Formula is C15H21N5O5. white to off-white crystalline powder trans-Zeatin-riboside is used in tissue culture systems include control of shoot growth and formation, cell division and inhibition of leaf senescence. Cytokinins promote cell division, stimulate shoot proliferation, inhibit root formation, slow the aging process, and activate gene expression and metabolic activity in general.

What is the CAS number for trans-Zeatin-riboside?

The CAS number of trans-Zeatin-riboside is 6025-53-2.

What is trans-Zeatin-riboside (6025-53-2) used for?

Trans-Zeatin-riboside is a naturally occurring plant hormone belonging to the cytokinin class. It is a 9-ribosylzeatin with trans-zeatin as the nucleobase. trans-Zeatin-riboside plays a crucial role in various aspects of plant growth and development, including cell division, shoot proliferation, and the inhibition of leaf senescence.InChI:InChI=1/C15H21N5O5/c1-8(5-21)2-3-16-14-11-9(4-18-19-14)20(7-17-11)15-13(24)12(23)10(6-22)25-15/h2,4,7,10,12-13,15,21-24H,3,5-6H2,1H3,(H,16,19)/t10-,12+,13+,15+/m1/s1

trans-Zeatin-riboside

CasNo:6025-53-2

Product Description

Cost-effective and customizable trans-Zeatin-riboside 6025-53-2 in stock

Molecular Formula: C15H21N5O5
Molecular Weight: 351.362
Appearance/Colour: white to off-white crystalline powder
Vapor Pressure: 4.42E-27mmHg at 25°C
Melting Point: 176-179 °C
Refractive Index: 1.728
Boiling Point: 731.8 °C at 760 mmHg
PKA: 13.11±0.70(Predicted)
Flash Point: 396.4 °C
PSA： 145.78000
Density: 1.65 g/cm³
LogP: -1.13870

trans-Zeatin-riboside(Cas 6025-53-2) Usage

Biochem/physiol Actions	Koenig RL; Morris RO; Polacco JC
Definition	ChEBI: A 9-ribosylzeatin having trans-zeatin as the nucleobase.

InChI:InChI=1/C15H21N5O5/c1-8(5-21)2-3-16-14-11-9(4-18-19-14)20(7-17-11)15-13(24)12(23)10(6-22)25-15/h2,4,7,10,12-13,15,21-24H,3,5-6H2,1H3,(H,16,19)/t10-,12+,13+,15+/m1/s1

6025-53-2 Relevant articles

Synthesis of [15N4] purine labeled cytokinin glycosides derived from zeatins and topolins with 9-β-d, 7-β-d-glucopyranosyl, or 9-β-d-ribofuranosyl group

Tranová, Lenka,Bu?ek, Jan,Zatloukal, Marek,Canka?, Petr,Styskala, Jakub

, p. 118 - 125 (2019/01/24)

Synthesis of [15N4] purine labeled cytok...

A purine nucleoside phosphorylase in Solanum tuberosum L. (potato) with specificity for cytokinins contributes to the duration of tuber endodormancy

Bromley, Jennifer R.,Warnes, Barbara J.,Newell, Christine A.,Thomson, Jamie C.P.,James, Celia M.,Turnbull, Colin G.N.,Hanke, David E.

, p. 225 - 237 (2014/03/21)

StCKP1 (Solanum tuberosum cytokinin ribo...

Peroxide-shunt substrate-specificity for the Salmonella typhimurium O 2-dependent tRNA modifying monooxygenase (MiaE)

Corder, Andra L.,Subedi, Bishnu P.,Zhang, Siai,Dark, Amanda M.,Foss Jr., Frank W.,Pierce, Brad S.

, p. 6182 - 6196 (2013/10/01)

Post-transcriptional modifications of tR...

Efficiency of different methods of extraction and purification of cytokinins

Hoyerova, Klara,Gaudinova, Alena,Malbeck, Jiri,Dobrev, Petre I.,Kocabek, Tomas,Solcova, Blanka,Travnickova, Alena,Kaminek, Miroslav

, p. 1151 - 1159 (2008/02/10)

The increasing use of advanced methods, ...

6025-53-2 Process route

: 2365-40-4
N₆-(2-isopentenyl)adenine

: 6025-53-2
trans-zeatin 9-β-D-ribofuranoside

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: trimethylsilyl trifluoromethanesulfonate / acetonitrile / 18 h / Reflux 2: sodium methylate; methanol / 6 h / 20 °C 3: Salmonella typhimurium O₂-dependent tRNA modifying monooxgenase; dihydrogen peroxide / dimethyl sulfoxide / 1 h / 27 °C / pH 8 / Enzymatic reaction With methanol; trimethylsilyl trifluoromethanesulfonate; Salmonella typhimurium O₂-dependent tRNA modifying monooxgenase; dihydrogen peroxide; sodium methylate; In dimethyl sulfoxide; acetonitrile; 1: \|Vorbrueggen Nucleoside Synthesis;

Yield

Multi-step reaction with 3 steps

1: trimethylsilyl trifluoromethanesulfonate / acetonitrile / 18 h / Reflux

2: sodium methylate; methanol / 6 h / 20 °C

3: Salmonella typhimurium O₂-dependent tRNA modifying monooxgenase; dihydrogen peroxide / dimethyl sulfoxide / 1 h / 27 °C / pH 8 / Enzymatic reaction

With methanol; trimethylsilyl trifluoromethanesulfonate; Salmonella typhimurium O₂-dependent tRNA modifying monooxgenase; dihydrogen peroxide; sodium methylate; In dimethyl sulfoxide; acetonitrile; 1: |Vorbrueggen Nucleoside Synthesis;