GLPBio

Thidiazuron

Catalog No.: GC45032Purity:>98.00%Synonyms: CCG-24904, SN 49537, TDZ
Thidiazuron belongs to bis-substituted urea derivatives, which showed extreme cytokinin activity and has been extensively used as an herbicide and a plant growth regulator.

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Thidiazuron
Cas No.: 51707-55-2
10mM (in 1mL DMSO)In Stock
$69.00
1
5gIn Stock
$63.00
1
10gIn Stock
$102.00
1

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Description

Thidiazuron belongs to bis-substituted urea derivatives, which showed extreme cytokinin activity and has been extensively used as an herbicide and a plant growth regulator [1]. Thidiazuron can affect multiple morphogenetic processes, including axillary shoot induction, adventitious shoot regeneration, and somatic embryogenesis in many plant species [2].

Thidiazuron (0~50μM; 24h) down-regulated the expression of uPA, uPAR, MMPs and VEGF in a dose-dependent manner in the MDA-MB-231 cells [3]. Thidiazuron (0, 0.025, 0.05, 0.1 and 0.4mg/L; 4 weeks) up-regulated the expression of cytokinin oxidase in the strawberry explants [2]. Thidiazuron (0, 2.3, 4.5, 6.9 and 9μM; 10 weeks) promoted somatic embryo formation in the blueberry leaf explants [4].

References:
[1] Nisler J. In Thidiazuron: From Urea Derivative to Plant Growth Regulator [M]. Berlin/Heidelberg, Germany: Springer, 2018.
[2] Wang F, Li Y, Pang Y, et al. Thidiazuron enhances strawberry shoot multiplication by regulating hormone signal transduction pathways [J]. International journal of molecular sciences, 2025, 26(9): 4060.
[3] Rajendran P, Ben Ammar R, Al-Saeedi F J, et al. Thidiazuron decreases epithelial-mesenchymal transition activity through the NF-kB and PI3K/AKT signalling pathways in breast cancer [J]. Journal of cellular and molecular medicine, 2020, 24(24): 14525-14538.
[4] Ghosh A, Igamberdiev A U, Debnath S C. Thidiazuron-induced somatic embryogenesis and changes of antioxidant properties in tissue cultures of half-high blueberry plants [J]. Scientific reports, 2018, 8(1): 16978.

Protocol

Cell experiment [1]:

Cell lines

MDA-MB-231 cells

Preparation Method

Cells were grown on four-chambered slides, exposed to Thidiazuron (50μM) for 2h, mounted and permeabilized. The cells were incubated with an anti-p65 antibody subsequently, FITC-labelled secondary antibody. The subcellular localization of p65 was examined through the confocal microscope at 40× magnification.

Reaction Conditions

50μM; 2h

Applications

Thidiazuron inhibited the nuclear translocation of p65.

References:
[1] Rajendran P, Ben Ammar R, Al-Saeedi F J, et al. Thidiazuron decreases epithelial-mesenchymal transition activity through the NF-kB and PI3K/AKT signalling pathways in breast cancer [J]. Journal of cellular and molecular medicine, 2020, 24(24): 14525-14538.

Product Documents

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Purity:>98.00%Appearance:A solid

Chemical Properties

CAS No.
51707-55-2
Synonyms
CCG-24904, SN 49537, TDZ
SMILES
O=C(NC1=CN=NS1)NC2=CC=CC=C2
Molecular Formula
C9H8N4OS
Molecular Weight
220.2
Solubility
DMF: 30 mg/ml,DMF:PBS(pH 7.2)(1:1): 0.5 mg/ml,DMSO: 15 mg/ml,Ethanol: 1 mg/ml
Storage
Store at -20°C
General tips
Select a suitable solvent according to the product solubility data. Once prepared, aliquot the stock solution to avoid repeated freeze-thaw cycles.
Use stock solutions within 6 months when stored at -80°C or within 1 month when stored at -20°C.
To improve solubility, warm the tube to 37°C and sonicate it for an appropriate period.
Shipping Condition
Evaluation samples are shipped with blue ice. Other available sizes are shipped at room temperature or with blue ice upon request.

CalculatorsMolarity / Dilution / Molecular Weight / Unit Conversion / In Vivo Formulation / Solubility

g/mol

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