Kinetin (Synonyms: N6-furfuryladenine, NSC 23119) |
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Catalog No.GC11023
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Kinetin is a plant hormone that can regulate gene expression, cell cycle and calcium flux.
Products are for research use only. Not for human use. We do not sell to patients.
Cas No.: 525-79-1
Sample solution is provided at 25 µL, 10mM.
Kinetin is a plant hormone that can regulate gene expression, cell cycle and calcium flux [1]. Kinetin can regulate DNA repair and proteosome-mediated protein turnover, and activate Arabidopsis cell division through induction of the d-type cyclin CycD3 [2]. Kinetin has been widely used to protects DNA against oxidative damage to 8-oxo-dG mediated by the Fenton reaction [3].
In vitro, Kinetin treatment (10μM) for 7 days significantly stimulated differentiation of C2C12 cells into myotubes [4]. Treatment with 40μM Kinetin for 2 days significantly inhibited the growth of keratinocytes and increased the levels of the Involucrin and K10 protein [5]. The 24-hour treatment with 500μM Kinetin significantly inhibited the viability of HL-60 cells[6].
In vivo, Kinetin treatment via oral administration at a dose of 20mg/kg daily for 90 days significantly improved cognitive impairment in mice induced by aluminum chloride and D-galactose, and reduced brain oxidative stress[7]. Daily intraperitoneal injection of 1mg/kg dose of Kinetin for 10 days significantly alleviated the oxidative stress in the liver of rats induced by cisplatin and reduced the levels of CRP, IL-6 and CD95[8].
References:
[1] Barciszewski J, Siboska G, Rattan S I S, et al. Occurrence, biosynthesis and properties of kinetin (N6-furfuryladenine)[J]. Plant growth regulation, 2000, 32(2): 257-265.
[2] Barciszewski J, Rattan S I S, Siboska G, et al. Kinetin—45 years on[J]. Plant science, 1999, 148(1): 37-45.
[3] Barciszewski J, Massino F, Clark B F C. Kinetin—a multiactive molecule[J]. International Journal of Biological Macromolecules, 2007, 40(3): 182-192.
[4] Mielcarek M, Isalan M. Kinetin stimulates differentiation of C2C12 myoblasts[J]. PLoS One, 2021, 16(10): e0258419.
[5] Berge U, Kristensen P, Rattan S I S. Kinetin‐induced differentiation of normal human keratinocytes undergoing aging in vitro[J]. Annals of the New York Academy of Sciences, 2006, 1067(1): 332-336.
[6] Naseem M, Othman E M, Fathy M, et al. Integrated structural and functional analysis of the protective effects of kinetin against oxidative stress in mammalian cellular systems[J]. Scientific reports, 2020, 10(1): 13330.
[7] Wei Y, Liu D, Zheng Y, et al. Protective effects of kinetin against aluminum chloride and D-galactose induced cognitive impairment and oxidative damage in mouse[J]. Brain research bulletin, 2017, 134: 262-272.
[8] Fathy M, Darwish M A, Abdelhamid A S M, et al. Kinetin ameliorates cisplatin-induced hepatotoxicity and lymphotoxicity via attenuating oxidative damage, cell apoptosis and inflammation in rats[J]. Biomedicines, 2022, 10(7): 1620.
| Cell experiment [1]: | |
Cell lines | HL-60 cells |
Preparation Method | HL-60 cells were grown in RPMI-1640 medium with 10% (v/v) fetal bovine serum (FBS), 1% (w/v) l-glutamine and 0.4% (w/v) antibiotics (50U/ml penicillin, and 50mg/ml streptomycin) at 37°C in 5% CO2/atmosphere. Cells were seeded at a density of 3.5×105 cells/ml in the 6-well plates and allowed to adhere in a 5% CO2 incubator at 37°C for 24h. The cells were treated with different concentrations of Kinetin (0, 0.5, 1, 10, 100, and 500μM) for 24h. The cell viability was evaluated. |
Reaction Conditions | 0, 0.5, 1, 10, 100, and 500μM; 24h |
Applications | Kinetin treatment significantly reduced cell viability of HL-60 cells in a dose-dependent manner. |
| Animal experiment [2]: | |
Animal models | Kunming mice |
Preparation Method | Kunming mice (18-22g) were housed singly in a standard environment with food and water ad libitum. After a one-week adaptation period, the mice were administered 20mg/kg of Kinetin orally daily, drank water containing 10mg/kg of aluminum chloride, and were given subcutaneous injections of D-galactose (100mg/kg/day) for 90 days. Then, the mouse brain tissues were collected for analysis. |
Dosage form | 20mg/kg/day; 90 days; p.o. |
Applications | Kinetin treatment significantly attenuated the histopathological changes in hippocampus CA3 region of mouse brain tissues. |
References: | |
| Cas No. | 525-79-1 | SDF | |
| Synonyms | N6-furfuryladenine, NSC 23119 | ||
| Chemical Name | N-(furan-2-ylmethyl)-7H-purin-6-amine | ||
| Canonical SMILES | C1=COC(=C1)CNC2=NC=NC3=C2NC=N3 | ||
| Formula | C10H9N5O | M.Wt | 215.21 |
| Solubility | ≥ 5.38 mg/mL in DMSO with gentle warming | Storage | Store at-20°C |
| General tips | Please select the appropriate solvent to prepare the stock solution according to the
solubility of the product in different solvents; once the solution is prepared, please store it in
separate packages to avoid product failure caused by repeated freezing and thawing.Storage method
and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored
at -20°C, please use it within 1 month. To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time. |
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| Shipping Condition | Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request. | ||
| Prepare stock solution | |||
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1 mg | 5 mg | 10 mg |
| 1 mM | 4.6466 mL | 23.2331 mL | 46.4662 mL |
| 5 mM | 929.3 μL | 4.6466 mL | 9.2932 mL |
| 10 mM | 464.7 μL | 2.3233 mL | 4.6466 mL |
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Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.
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Quality Control & SDS
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- Purity: >99.50% Appearance: A solid
- COA (Certificate of Analysis)
- SDS (Safety Data Sheet)
- Datasheet
Average Rating: 5 (Based on Reviews and 30 reference(s) in Google Scholar.)















