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39777-61-2

中文名稱(chēng) (1E,4E)-1,5(2 -甲氧基苯基)-1,4-戊二烯-3-酮
英文名稱(chēng) (1E,4E)-1,5-Bis(2-Methoxyphenyl)penta-1,4-dien-3-one
CAS 39777-61-2
分子式 C19H18O3
分子量 294.34
MOL 文件 39777-61-2.mol
更新日期 2024/05/29 21:49:36
39777-61-2 結(jié)構(gòu)式 39777-61-2 結(jié)構(gòu)式

基本信息

中文別名
(1E,4E)-1,5-二(2-甲氧基)-1,4-二烯基-3-戊酮
(1E,4E)-1,5(2 -甲氧基苯基)-1,4-戊二烯-3-酮
英文別名
RPN77612
TFEB activator 1
Curcumin analog C1
Curcumin analog compound C1
Curcumin analog C1(TFEB activator 1 )
(1E,4E)-1,5-Bis(2-Methoxyphenyl)penta-1
1,5-Bis-(2-methoxy-phenyl)-penta-1,4-dien-3-one
(1E,4E)-1,5-Bis(2-Methoxyphenyl)penta-1,4-dien-3-one
(1E,4E)-1,5-Bis(2-methoxyphenyl)-1,4-pentadien-3-one
1,4-Pentadien-3-one, 1,5-bis(2-Methoxyphenyl)-, (1E,4E)-
所屬類(lèi)別
生物:抑制劑激活劑

物理化學(xué)性質(zhì)

熔點(diǎn)120-122 °C(Solv: ethanol (64-17-5); water (7732-18-5))
沸點(diǎn)467.2±40.0 °C(Predicted)
密度1.128±0.06 g/cm3(Predicted)
儲(chǔ)存條件Sealed in dry,2-8°C
溶解度DMSO: 125 mg/mL (424.68 mM)
形態(tài)固體
顏色Light yellow to yellow

安全數(shù)據(jù)

危險(xiǎn)性符號(hào)(GHS)GHS hazard pictograms
GHS07
警示詞警告
危險(xiǎn)性描述H302-H319-H315-H335

常見(jiàn)問(wèn)題列表

生物活性
Curcumin analog C1 (Curcumin analog Compound C1)是有效的 transcription factor EB (TFEB) 激活劑,有望用于預(yù)防或治療阿爾茨海默氏病。
靶點(diǎn)
TargetValue
TFEB
()
體外研究

TFEB activator 1 (Compound C1) activates TFEB (transcription factor EB) by directly binding to TFEB and promotes its entry into the nucleus, without affecting TFEB phosphorylation or inhibiting the activities of MTOR and MAPK1/ERK2-MAPK3/ERK1.
TFEB activator 1 (1 μM; for 12 h) significantly increases the levels of LC3B-II, the lipidated and phagophore- or autophagosome-associated form of MAP1LC3B/LC3B (microtubule-associated protein 1 light chain 3 β) in N2a cells.
TFEB activator 1 (0.2-1 μM) dose-dependently increases the levels of LC3-II and SQSTM1/p62 (sequestosome 1) in N2a cells.

Western Blot Analysis

Cell Line: N2a cells
Concentration: 0, 0.2, 0.4, 0.6, 0.8 and 1 μM
Incubation Time: 12 hours
Result: Treatment dose-dependently increased the levels of LC3-II and SQSTM1/p62 (sequestosome 1).
體內(nèi)研究

The medium lethal dose (LD 50 ) value of TFEB activator 1 (Compound C1) is 175 mg/kg in the acute toxicity assay (single-dose i.v. tail vein injection; in rats) .
Short-term oral administration of TFEB activator 1 (low dosage 10 mg/kg and high dosage 25 mg/kg; for 24 h) dose-dependently increases the expression of LC3B-II and TFEB in the liver, frontal cortex and striatum of the brain.
Chronic administration of TFEB activator 1 (10 mg/kg per day; orally administered by gavage) activates TFEB and enhances autophagy in rat brains.

Animal Model: Adult male Sprague-Dawley (SD) rats weighing 350 to 400 g
Dosage: 10 mg/kg and 25 mg/kg
Administration: Short-term oral administration; for 24 hours
Result: Activated TFEB and enhanced autophagy and lysosome biogenesis in rat brain.
Animal Model: Adult male Sprague-Dawley (SD) rats weighing 350 to 400 g
Dosage: 10 mg/kg
Administration: Chronic oral administration; daily; for 21 days
Result: Activated TFEB and enhanced autophagy in rat brains.
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