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1137359-47-7

中文名稱 BRD7552
英文名稱 ethyl 4-(((2R,3R,4S,5R,6S)-4,5-bis(benzo[d][1,3]dioxol-5-ylcarbamoyloxy)-2-(hydroxymethyl)-6-methoxy-tetrahydro-2H-pyran-3-yloxy)carbonyl)benzoate
CAS 1137359-47-7
分子式 C33H33N3O15
分子量 711.63
MOL 文件 1137359-47-7.mol
更新日期 2024/10/28 11:14:31
1137359-47-7 結(jié)構(gòu)式 1137359-47-7 結(jié)構(gòu)式

基本信息

中文別名
4-(((((2R,3R,4S,5R,6S)-4,5-雙((苯并[D][1,3]二氧戊環(huán)-5-基氨基甲?;?氧基)-2-(羥甲基)-6-甲氧基四氫-2H-吡喃-3-基)氧基)羰基)氨基)苯甲酸乙酯
英文別名
CS-1560
BRD7552
BRD7552 >=98% (HPLC)
BRD 7552
BRD-7552
BRD7552
Methyl [2,3-O-bis(Benzo[1,3]dioxol-5-yl-carbamoyl)]-4-O-(4-ethoxycarbonyl-phenylcarbamoyl)-α-D-glucopyranoside
α-D-Glucopyranoside, methyl, 2,3-bis(N-1,3-benzodioxol-5-ylcarbamate) 4-[N-[4-(ethoxycarbonyl)phenyl]carbamate]
ethyl 4-(((2R,3R,4S,5R,6S)-4,5-bis(benzo[d][1,3]dioxol-5-ylcarbamoyloxy)-2-(hydroxymethyl)-6-methoxy-tetrahydro-2H-pyran-3-yloxy)carbonyl)benzoate
所屬類別
生物化工:激動劑抑制劑

物理化學性質(zhì)

沸點757.6±60.0 °C(Predicted)
密度1.53±0.1 g/cm3(Predicted)
儲存條件-20°C儲存
溶解度DMF: 25 mg/ml; DMF:PBS (pH 7.2) (1:5): 0.2 mg/ml; DMSO: 20 mg/ml; Ethanol: 10 mg/ml
酸度系數(shù)(pKa)11.81±0.20(Predicted)
形態(tài)結(jié)晶固體
顏色White to off-white

常見問題列表

生物活性
BRD7552 是一種 PDX1 轉(zhuǎn)錄因子誘導劑,它上調(diào)了人類原代胰島和導管細胞中 PDX1 的表達,并誘導 PDX1 啟動子的表觀遺傳變化與轉(zhuǎn)錄激活一致。BRD7552 增加胰島素表達。PDX1 是參與胰腺發(fā)育和β細胞功能的關鍵轉(zhuǎn)錄因子。
體外研究

BRD7552 (0-5 μM; 5 days) induces a dose-dependent increase in PDX1 protein levels after BRD7552 treatment in PANC-1 cells.
BRD7552 acts in a FOXA2-dependent manner to increase PDX1 expression in human ductal cells. Nine-day treatment of PANC-1 cells with BRD7552 (0-10 μM) causes a dose-dependent increase in insulin mRNA expression. BRD7552 induces insulin expression in PANC-1 cells. BRD7552 increases H3 acetylation and H3K4me3 and decreases H3K9me3, results that are consistent with transcriptional activation of PDX1. The epigenetic changes induced by BRD7552 are consistent with transcriptional activation, and BRD7552 acts in a FOXA2-dependent manner.

Western Blot Analysis

Cell Line: PANC-1 cells
Concentration: 1.25, 2.5, 5 μM
Incubation Time: 5 days
Result: Induced a dose-dependent increase in PDX1 protein levels.
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