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K3000

Sigma-Aldrich

Kinetin riboside

proapoptotic anitproliferative plant growth regulator

Sinonimo/i:

6-Furfurylaminopurine riboside, N6-(2-Furanyl­methyl)adenosine, N6-Furfuryladenosine

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About This Item

Formula empirica (notazione di Hill):
C15H17N5O5
Numero CAS:
4338-47-0
Peso molecolare:
347.33
Numero CE:
224-389-3
Numero MDL:
MFCD00037987
Codice UNSPSC:
12352207
ID PubChem:
24896224
NACRES:
NA.72

Saggio

≥98% (HPLC)
≥98% (TLC)

Forma fisica

powder

Solubilità

acetic acid: 49.00-51.00 mg/mL, clear, colorless to yellow

Temperatura di conservazione

2-8°C

Stringa SMILE

OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n2cnc3c(NCc4ccco4)ncnc23

InChI

1S/C15H17N5O5/c21-5-9-11(22)12(23)15(25-9)20-7-19-10-13(17-6-18-14(10)20)16-4-8-2-1-3-24-8/h1-3,6-7,9,11-12,15,21-23H,4-5H2,(H,16,17,18)/t9-,11-,12-,15-/m1/s1
CAGLGYNQQSIUGX-SDBHATRESA-N

Informazioni sul gene

rat ... Adora1(29290) , Adora2a(25369) , Adora3(25370)

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Descrizione generale

Kinetin riboside is a ribosylated form of kinetin. It is a natural cytokinin plant hormone.

Applicazioni

Kinetin riboside may be used:
  • to study its cytotoxic effects on plant and animal tumor cells
  • to investigate its apoptotic effects in both cancer and immortalized cells
  • to elucidate its influence on human prostate cell epithelial-mesenchymal transition in vitro

Azioni biochim/fisiol

Kinetin riboside exhibits cytotoxic and antiproliferative activities. In addition, it also shows anticancer activity by inducing apoptosis in various types of cancers including myeloid leukemia cells, mouse melanoma B16F-10 cells, and plant tumor cells.

Codice della classe di stoccaggio

13 - Non Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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Sigma-Aldrich

M5519

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Bernard Griffaut et al.
International journal of biological macromolecules, 34(4), 271-275 (2004-09-18)
The cytotoxicity of two plant hormone compounds, kinetin and kinetin riboside, was studied on tumour cells, by colony forming assay with increased amount of cytotoxic molecules. The concentration of inhibitor required to reduce cell growth to 50% was determined for
Dennison Trinh et al.
Journal of neurochemistry, 156(6), 715-752 (2021-02-23)
Mitochondria are essential for neuronal function. They produce ATP to meet energy demands, regulate homeostasis of ion levels such as calcium and regulate reactive oxygen species that cause oxidative cellular stress. Mitochondria have also been shown to regulate protein synthesis
Effects of kinetin riboside on proliferation and proapoptotic activities in human normal and cancer cell lines.
Dudzik P, Dulinska-Litewka J, Wyszko E, et al.
The Journal of Cell Biology, 112, 2115-2124 (2011)
Zhenfang Cheng et al.
Journal of separation science, 41(11), 2386-2392 (2018-02-24)
In this work, an easy, effective, and sensitive method based on graphene oxide@silica@magnetite composites as adsorbent of magnetic solid-phase extraction combined with liquid chromatography and tandem mass spectrometry, was established and validated for the trace analysis of cytokinins in different
Bo-Hwa Choi et al.
Cancer letters, 261(1), 37-45 (2007-12-29)
Here, we demonstrate that kinetin riboside (KR), a cytokinin analog, induces apoptosis in HeLa and mouse melanoma B16F-10 cells. KR disrupted the mitochondrial membrane potential and induced the release of cytochrome c and activation of caspase-3. Bad were upregulated while
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