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287194-40-5

中文名稱 287194-40-5
英文名稱 DEHYDROXYMETHYLEPOXYQUINOMICIN
CAS 287194-40-5
分子式 C13H11NO5
分子量 261.23
MOL 文件 287194-40-5.mol
更新日期 2024/11/15 18:20:32
287194-40-5 結構式 287194-40-5 結構式

基本信息

中文別名
(-)-DHMEQ
NF-ΚB抑制劑((+)-DHMEQ)
2-羥基-N-(((1S,2S,6S)-2-羥基-5-氧代-7-氧雜雙環(huán)[4.1.0]庚-3-烯-3-基)苯甲酰胺
英文別名
DHMEQ
DHM2EQ
DEHYDROXYMETHYLEPOXYQUINOMICIN
Dehydroxymethylepoxyquinomicin (DHMEQ)
(-)-DHMEQ?(dehydroxymethylepoxyquinomicin)
2-hydroxy-N-[(1S,2S,6S)-2-hydroxy-5-oxo-7-oxabicyclo[4.1.0]hept-3-en-3-yl]benzaMide
Benzamide, 2-hydroxy-N-[(1S,2S,6S)-2-hydroxy-5-oxo-7-oxabicyclo[4.1.0]hept-3-en-3-yl]-

物理化學性質

熔點187 °C
沸點617.2±55.0 °C(Predicted)
密度1.58±0.1 g/cm3(Predicted)
儲存條件-20°C儲存
溶解度DMSO : ≥ 32 mg/mL (122.50 mM)
酸度系數(pKa)8.43±0.30(Predicted)
形態(tài)Solid
顏色Off-white to gray

安全數據

危險性符號(GHS)有害 (GHS07)
GHS07
警示詞警告
危險性描述H302-H315-H319-H335

常見問題列表

生物活性
(-)-DHMEQ (Dehydroxymethylepoxyquinomicin) 是一種有效,選擇性且不可逆的 NF-κB 抑制劑,與半胱氨酸殘基共價結合。(-)-DHMEQ 抑制 NF-κB 的核易位,并顯示抗炎和抗癌活性。
靶點

RelA

RelB

體外研究

(-)-DHMEQ (Dehydroxymethylepoxyquinomicin; 2-10 μg/mL; 12-48 hours) treatment significantly reduces the viability of all cell lines in a dose- and time-dependent manner, whereas the effect is not significant in a control cell line K562 without constitutive NF-κB activity.
(-)-DHMEQ (10 μg/mL; 0-48 hours; TL-Om1, MT-1 and K562 cells) treatment significantly increases the Annexin V-positive cells in MT-1 and TL-Om1 cell lines.
(-)-DHMEQ (10 μg/mL; 4-16 hours; MT-1 cells) treatment down-regulates Bcl-xL, Bcl-2, c-myc, cyclin D1, Rb, and p53, and up-regulates proapoptotic genes such as caspase-3, -8, and-9.
(-)-DHMEQ treatment increases cells in G0 /G1 phase in a time-dependent manner, demonstrating antiproliferative effects of (-)-DHMEQ.
(-)-DHMEQ binds to p65, cRel, RelB, and p50, but not to p52 at specific cysteine residues. (-)-DHMEQ inhibits not only DNA-binding of RelB, but also its interaction to importin. (-)-DHMEQ also induces instability of RelB.

Cell Proliferation Assay

Cell Line: TL-Om1, MT-1, KK-1, ST-1 and K562 cells
Concentration: 2 μg/mL, 5 μg/mL, 10 μg/mL
Incubation Time: 12 hours, 24 hours, 48 hours
Result: Significantly reduced the viability of all cell lines in a dose- and time-dependent manner.

Apoptosis Analysis

Cell Line: TL-Om1, MT-1 and K562 cells
Concentration: 10 μg/mL
Incubation Time: 0 hours, 24 hours, 48 hours
Result: Annexin V-positive cells were significantly increased after 24 to 48 hours.

Western Blot Analysis

Cell Line: MT-1 cells
Concentration: 10 μg/mL
Incubation Time: 4 hours, 8 hours, 16 hours
Result: Annexin V-positive cells were significantly increased after 24 to 48 hours.
體內研究

(-)-DHMEQ (Dehydroxymethylepoxyquinomicin; 4 mg/kg or 12 mg/kg; intraperitoneal injection; on day 0 and 3 times a week; for one month; SCID mice) treatment shows a significant increase in the survival rate in mice.

Animal Model: Male C.B17-scid/scid (5 weeks old) mice injected with MT-2 cells
Dosage: 4 mg/kg or 12 mg/kg
Administration: Intraperitoneal injection; on day 0 and 3 times a week; for one month
Result: Showed a significant increase in the survival rate in mice.
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