Name | kinetin |
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Synonyms |
6-Furfurylaminopurine,N6-Furfuryladenine
N-(2-Furylmethyl)-7H-purin-6-amine N-furfuryl-7H-purin-6-amine N-(2-Furylmethyl)-3H-purin-6-amine N-(Furan-2-ylmethyl)-1H-purin-6-amine MFCD00075757 7H-Purin-6-amine, N-(2-furanylmethyl)- T56 BM DN FN HNJ IM1- BT5OJ cytokinin fap EINECS 208-382-2 N-(2-furanylmethyl)-1H-purin-6-amine QUINETINE 6-(Furfurylamino)purine Kinetin N-Furfuryl-Adenine Kiniten N6-Furfuryladenine N-(Furan-2-ylmethyl)-9H-purin-6-amine 3H-Purin-6-amine, N-(2-furanylmethyl)- 6-Furfurylaminopurine KINETINE N6-(2-Furylmethyl)-9H-purin-6-amine N(Sup6)-Furfuryladenine N-(furan-2-ylmethyl)-7H-purin-6-amine Adenine, N-furfuryl- N-Furfuryladenine Kinetina T56 BM DN GN INJ FM1- BT5OJ |
Description | Kinetin (N6-furfuryladenine) belongs to a group of plant growth hormones involved in cell division, differentiation and other physiological processes.IC50 Value: Target:Kinetin is one of the widely used components in numerous skin care cosmetics and cosmeceuticals, such as Valeant products kinerase. Recently, kinetin has the potential to be a treatment for the human splicing disease familial dysautonomia.in vitro: Kinetin-induced cell death reflected by the morphological changes of nuclei including their invagination, volume increase, chromatin condensation and degradation as well as formation of micronuclei showed by AO/EB and 4,6-diamidino-2-phenylindol staining was accompanied by changes including increase in conductivity of cell electrolytes secreted to culture media, decrease in the number of the G1- and G2-phase cells and appearance of fraction of hypoploid cells as the effect of DNA degradation without ladder formation [1]. The plant cytokinin kinetin dramatically increases exon 20 inclusion in RNA isolated from cultured FD cells [3].in vivo: Subjects received 23.5 mg/Kg/d for 28 d. An increase in WT IKBKAP mRNA expression in leukocytes was noted after 8 d in six of eight individuals; after 28 d, the mean increase compared with baseline was significant (p = 0.002) [2].Toxicity: On mice with leukaemia P388, kinetin has no effect on the tumour growth, and it appears to be toxic at the dose of 25 mg/kg [4]. |
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Related Catalog | |
References |
Density | 1.6±0.1 g/cm3 |
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Boiling Point | 367.6±52.0 °C at 760 mmHg |
Melting Point | 269-271 °C (dec.)(lit.) |
Molecular Formula | C10H9N5O |
Molecular Weight | 215.211 |
Flash Point | 176.1±30.7 °C |
Exact Mass | 215.080704 |
PSA | 79.63000 |
LogP | -0.56 |
Vapour Pressure | 0.0±0.8 mmHg at 25°C |
Index of Refraction | 1.774 |
Storage condition | −20°C |
Water Solubility | H2O: soluble |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
MUTATION DATA
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Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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Hazard Codes | Xi |
Risk Phrases | 68-36/37/38 |
Safety Phrases | S23-S24/25-S22 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
RTECS | AU6270000 |
HS Code | 29349990 |
Precursor 9 | |
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DownStream 8 | |
HS Code | 2934999090 |
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Summary | 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |