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Генистеин
- английское имяGenistein
- CAS №446-72-0
- CBNumberCB6163787
- ФормулаC15H10O5
- мольный вес270.24
- EINECS207-174-9
- номер MDLMFCD00016952
- файл Mol446-72-0.mol
химическое свойство
Температура плавления | 297-298 °C |
Температура кипения | 333.35°C (rough estimate) |
плотность | 1.2319 (rough estimate) |
показатель преломления | 1.6000 (estimate) |
температура хранения | -20°C |
растворимость | DMSO: soluble |
форма | powder |
пка | 6.51±0.20(Predicted) |
цвет | off-white |
Биологические источники | synthetic |
Растворимость в воде | insoluble |
Мерк | 14,4391 |
БРН | 263823 |
Стабильность | Light Sensitive |
ИнЧИКей | TZBJGXHYKVUXJN-UHFFFAOYSA-N |
LogP | 3.114 (est) |
Справочник по базе данных CAS | 446-72-0(CAS DataBase Reference) |
Рейтинг продуктов питания EWG | 1 |
Словарь онкологических терминов NCI | genistein |
FDA UNII | DH2M523P0H |
Словарь наркотиков NCI | genistein |
Система регистрации веществ EPA | 4H-1-Benzopyran-4-one, 5,7-dihydroxy-3-(4-hydroxyphenyl)- (446-72-0) |
UNSPSC Code | 85151701 |
NACRES | NA.77 |
больше
Коды опасности | Xi,Xn | |||||||||
Заявления о рисках | 36/38-22 | |||||||||
Заявления о безопасности | 26-24/25-22 | |||||||||
WGK Германия | 3 | |||||||||
RTECS | NR2392000 | |||||||||
TSCA | Yes | |||||||||
Класс опасности | IRRITANT | |||||||||
кода HS | 29329990 | |||||||||
Банк данных об опасных веществах | 446-72-0(Hazardous Substances Data) | |||||||||
NFPA 704: |
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рисовальное письмо(GHS)
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рисовальное письмо(GHS)
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сигнальный язык
предупреждение
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вредная бумага
H302:Вредно при проглатывании.
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оператор предупредительных мер
P264:После работы тщательно вымыть кожу.
P270:При использовании продукции не курить, не пить, не принимать пищу.
P301+P312:ПРИ ПРОГЛАТЫВАНИИ: Обратиться за медицинской помощью при плохом самочувствии.
P501:Удалить содержимое/ контейнер на утвержденных станциях утилизации отходов.
Генистеин химические свойства, назначение, производство
Химические свойства
Yellow Crystalline SolidИспользование
Exhibits specific inhibitory activity against tyrosine kinases,including autophosphorylation of epidermal growth factor receptor kinase (IC50 - 2.6uM). Also inhibits other protein kinases through competitive inhibition of ATP. Inhibits tumor cell proliferation and induces tumor cell differentiation. Produces cell-cycle arrest and apoptosis in Jurat T-leukemia cells. However, it prevents anti-CD3 monoclonal antibody-induced thymic apoptosis. Genistein also inhibits topoisomerase II activity in vitro. Genistein has also been shown to inhibit the action of GABA on recombinant GABAA receptors 2. uv(max)ethanol: 262.5 nm (e= 138). moderately sol. in hot alcoholОпределение
ChEBI: 7-Hydroxyisoflavone with additional hydroxy groups at positions 5 and 4'. It is a phytoestrogenic isoflavone with antioxidant properties.Общее описание
Pharmaceutical secondary standards for application in quality control provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standardsБиологическая активность
Phytoestrogen with a wide range of biological actions. Inhibits protein tyrosine kinases including epidermal growth factor receptor kinase. Also binds to PPAR γ and estrogen receptors and acts as an agonist at GPR30. Also available as part of the MAPK Cascade Inhibitor Tocriset™ .Механизм действия
Genistein, an isoflavone isolated from soybeans, exhibits anticarcinogenic and antioxidant properties. Particularly, genistein has been shown to inhibit production of IL-6 and MAPK. Modulation to these cellular events may help regulate and attenuate UVB-induced inflammatory damage to the skin. Moreover, genistein inhibits UV-induced oxidative DNA damage and blocks UV-induced expression of c-fos and c-jun proto-oncogenes.разработк И противоопухолевых препаратов
It is an isoflavone and is obtained from a variety of plants like psoralea (Psoraleacorylifolia), kudzu (Pueraria lobata), faba beans (Vicia faba), and soybeans(Glycine max). It exhibits anticancer effect by inhibiting NF-κB and protein kinaseB (Akt) signaling pathways (Singh et al. 2016b). It blocks the proliferation of cancercells via the inhibition of cell growth enzymes and survival like tyrosine kinase andtopoisomerase II; hence it is used to treat leukemia. Genistein increases the growthrate of some estrogen receptors in breast cancer cells and the rate of proliferation of estrogen-dependent breast cancer by competitive binding to the estrogen-β receptors.It may be involved in JNK pathway in inducing activator protein-1(AP-1) activity(Wang et al. 2012; Dixon and Ferreira 2002).Профиль безопасности
Experimental reproductive effects. Human mutation data reported. When heated to decomposition it emits acrid smoke and irritating fumes.Методы очистки
Crystallise it from EtOH or aqueous EtOH. It has UV: max at 290nm (EtOH). The S(-)-enantiomer (natural form) has m 255-256o (from EtOH) and [] D 20 -28.0o (c 2, EtOH), [ ] D 20 -35.2o (c 1, pyridine).[Beilstein 18 H 503, 18 II 164, 18 III/IV 2630.] Genistein (4',5,7-trihydroxyisoflavone) [446-72-0]M 270.2 crystallises from 60% aqueous EtOH or water with m 297-298o and [] D 20 -28o (c 0.6, 20mM NaOH). [Beilstein 18/4 V 594.]For Naringin (naringenin 7-rhamnoglucoside) See “Carbohydrates” in Chapter 6.Генистеин запасные части и сырье
Генистеин поставщик
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