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1395084-25-9

中文名稱 (E)-4-((2-AMINO-4-HYDROXY-5-METHYLPHENYL)DIAZENYL)-N-(PYRIDIN-2-YL)BENZENESULFONAMIDE
英文名稱 MS436
CAS 1395084-25-9
分子式 C18H17N5O3S
分子量 383.42
MOL 文件 1395084-25-9.mol
更新日期 2024/12/24 19:29:54
1395084-25-9 結(jié)構(gòu)式 1395084-25-9 結(jié)構(gòu)式

基本信息

中文別名
BROMODOMAIN抑制劑(MS436)
4-[(1E)-2-(2-氨基-4-羥基-5-甲基苯基)偶氮]-N-2-吡啶基苯磺酰胺
英文別名
MS436
CS-1882
MS436(95%)
MS 436, >=98%
MS-436
MS 436
MS436 USP/EP/BP
(E)-4-[2-(2-Amino-4-hydroxy-5-methylphenyl)diazenyl]-N-2-pyridinylbenzenesulfonamide
(E)-4-((2-AMINO-4-HYDROXY-5-METHYLPHENYL)DIAZENYL)-N-(PYRIDIN-2-YL)BENZENESULFONAMIDE
4-[(1E)-2-(2-Amino-4-hydroxy-5-methylphenyl)diazenyl]-N-2-pyridinylbenzenesulfonamide
Benzenesulfonamide, 4-[(1E)-2-(2-amino-4-hydroxy-5-methylphenyl)diazenyl]-N-2-pyridinyl-
所屬類別
生物化工:Epigenetic Reader Domain 抑制劑

物理化學(xué)性質(zhì)

沸點(diǎn)673.7±65.0 °C(Predicted)
密度1.42±0.1 g/cm3(Predicted)
儲存條件-20°C儲存
溶解度insoluble in H2O; insoluble in EtOH; ≥19.15 mg/mL in DMSO
酸度系數(shù)(pKa)9.25±0.36(Predicted)
形態(tài)固體
顏色Pink to red
(E)-4-((2-AMINO-4-HYDROXY-5-METHYLPHENYL)DIAZENYL)-N-(PYRIDIN-2-YL)BENZENESULFONAMIDE價格(試劑級)
報價日期產(chǎn)品編號產(chǎn)品名稱CAS號包裝價格
2024/11/11XW1395084259014-[(1E)-2-(2-氨基-4-羥基-5-甲基苯基)偶氮]-N-2-吡啶基苯磺酰胺1395084-25-950MG3696元
2024/11/08HY-13959(E)-4-((2-AMINO-4-HYDROXY-5-METHYLPHENYL)DIAZENYL)-N-(PYRIDIN-2-YL)BENZENESULFONAMIDE
MS436
1395084-25-95mg750元
2024/11/08HY-13959(E)-4-((2-AMINO-4-HYDROXY-5-METHYLPHENYL)DIAZENYL)-N-(PYRIDIN-2-YL)BENZENESULFONAMIDE
MS436
1395084-25-910mM * 1mLin DMSO825元

常見問題列表

生物活性
MS436 是一種 bromodomain 抑制劑,有效作用于 BRD4 BrD1,Ki 為 30-50 nM,比作用于 BrD2 選擇性高 10 倍。
靶點(diǎn)

Ki: 30-50 nM (BRD4 bromodomain)

體外研究

MS436, through a set of water-mediated interactions, exhibits low nanomolar affinity (estimated K i of 30-50 nM) with preference for the first bromodomain over the second. MS436 effectively inhibits BRD4 activity in NF-κB-directed production of NO and pro-inflammatory cytokine interleukin-6 in murine macrophages. MS436 represents a new class of bromodomain inhibitors and will facilitate further investigation of the biological functions of the two bromodomains of BRD4 in gene expression. MS436 exhibits potent affinity of an estimated K i =30-50 nM for the BRD4 BrD1 and a 10-fold selectivity over the BrD2, which is achieved through a unique set of water-mediated intermolecular interactions.

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