Основные атрибуты  химическое свойство Информация о безопасности химические свойства, назначение, производство запасные части и сырье поставщик Обзор
 структурированное изображение

6-Shogaol

  • русский язык имя
  • английское имя6-Shogaol
  • CAS №555-66-8
  • CBNumberCB4748322
  • ФормулаC17H24O3
  • мольный вес276.37
  • номер MDLMFCD01736094
  • файл Mol555-66-8.mol
химическое свойство
Температура кипения 427.5±35.0 °C(Predicted)
плотность 1.0448 g/cm3(Temp: 25 °C)
температура хранения Keep in dark place,Inert atmosphere,2-8°C
растворимость Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
пка 10.01±0.20(Predicted)
форма Liquid
цвет Colourless to Light Yellow
Запах Mild, warm-herbaceous, sweet odor
БРН 2056098
InChI InChI=1S/C17H24O3/c1-3-4-5-6-7-8-15(18)11-9-14-10-12-16(19)17(13-14)20-2/h7-8,10,12-13,19H,3-6,9,11H2,1-2H3
ИнЧИКей OQWKEEOHDMUXEO-BQYQJAHWSA-N
SMILES C(C1=CC=C(O)C(OC)=C1)CC(=O)C=CCCCCC
LogP 3.789 (est)
Справочник по базе данных CAS 555-66-8(CAS DataBase Reference)
FDA UNII 83DNB5FIRF
Справочник по химии NIST 6-shogaol(555-66-8)
UNSPSC Code 85151701
NACRES NA.25
Заявления об опасности и безопасности
Коды опасности Xn
Заявления о рисках 22
WGK Германия 3
NFPA 704:
3
0 0

рисовальное письмо(GHS)

  • рисовальное письмо(GHS)

    GHS hazard pictograms

  • сигнальный язык

    предупреждение

  • вредная бумага

    H302:Вредно при проглатывании.

  • оператор предупредительных мер

    P261:Избегать вдыхания пыли/ дыма/ газа/ тумана/ паров/ аэрозолей.

    P280:Использовать перчатки/ средства защиты глаз/ лица.

    P301+P312:ПРИ ПРОГЛАТЫВАНИИ: Обратиться за медицинской помощью при плохом самочувствии.

    P302+P352:ПРИ ПОПАДАНИИ НА КОЖУ: Промыть большим количеством воды.

    P305+P351+P338:ПРИ ПОПАДАНИИ В ГЛАЗА: Осторожно промыть глаза водой в течение нескольких минут. Снять контактные линзы, если Вы ими пользуетесь и если это легко сделать. Продолжить промывание глаз.

6-Shogaol химические свойства, назначение, производство

Химические свойства

White crystalline powder. B.P. higher than 300℃. Very slightly soluble in water, soluble in alcohol and oils.

Использование

[6]-Shogaol is an aromatic constituent of ginger and the chain-dehydroxylated analog of [6]-Gingerol. [6]-Shogaol has activity very similar to [6]-Gingerol and produced an inhibition of spontaneous motor activity, antipyretic and analgesic effects, and prolonged hexobarbital-induced sleeping time. [6]-Shogaol also has potent antitussive activity and affected the cortical EEG.

прикладной

Shogaol has little or no application in perfumery, and very little interest to the flavor industry, but it is included in this work mainly for the purpose of elucidating the problems apparently existing around the description of the odorand flavor of "Zingerone".

разработк И противоопухолевых препаратов

6-Shogaol is the dehydrated product of 6-gingerol, extracted from the rhizome ofginger. Treatment of HCC cell line with 6-shogaol resulted in cells with apoptoticphenotypes, which showed signs of cell and nuclear shrinkage as well as substantialchromatin condensation. De-phosphorylation of PERK and activation of theexpression of CHOP initiate caspase cascade reaction inducing apoptosis inHCC. Two-dimensional gel electrophoretic analysis of proteome revealed that in response to the treatment with 6-shogaol, a significant stimulation was observed inproteins related to the ER stress, signifying that apoptosis induced by 6-shogoal didinvolve ER stress. Cells showed marked rise in the UPR target expression, HSP70,Grp94, Grp78/Bip and the other ER chaperones on exposure to 6-shogoal in a time-dependentmanner, which elicited activation of caspase-3 and degradation of polyADP ribose polymerase (PARP). Various ER chaperone proteins improve adaptationof cancer cells to hypoxic environment and aid in developing resistance againstanticancer therapy (Zorzi and Bonvini 2011; Urra et al. 2016). Screening of specificinhibitors of Grp78 as antitumour agents (Hu et al. 2012; Liu et al. 2013; Venkatesanet al. 2015) implies that inhibition of Grp78/Bip is a very promising anticancerstrategy. HCC cells are selectively killed by 6-shogaol in the absence of anynoticeable toxic consequence on normal healthy cells and very little toxicity asstudied on SMMC7721 xenograft mice. Administration of 6-shogaol and salubrinaltogether for distinct time intervals resulted in significant increase in ER stress in thecell. It appears that 6-shogaol in combination with salubrinal has great therapeuticvalue against various malignancies including HCC (Hu et al. 2012).

6-Shogaol запасные части и сырье

запасной предмет

6-Shogaol поставщик

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