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返回ChemicalBook首頁>CAS數(shù)據(jù)庫列表>1210945-69-9

1210945-69-9

中文名稱 CS-1273
英文名稱 EG00229
CAS 1210945-69-9
分子式 C19H20F3N7O7S3
分子量 611.59
MOL 文件 1210945-69-9.mol
更新日期 2023/11/10 17:22:03
1210945-69-9 結(jié)構(gòu)式 1210945-69-9 結(jié)構(gòu)式

基本信息

中文別名
化合物 T11153
英文別名
CS-1273
EG00229
EG 00229 Trifluoroacetate
所屬類別
生物化工:激動劑抑制劑

物理化學(xué)性質(zhì)

儲存條件-20°C儲存
溶解度溶于二甲基亞砜
形態(tài)粉末
顏色Light yellow to yellow
CS-1273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
2026/06/05HY-10799EG002291210945-69-91 mg636元
2026/06/05HY-10799CS-1273
EG00229
1210945-69-95mg1400元
2026/06/05HY-10799CS-1273
EG00229
1210945-69-910mM * 1mLin DMSO1884元

常見問題列表

生物活性
EG00229 是一種神經(jīng)纖維蛋白 1 受體 (NRP1) 拮抗劑。EG00229 選擇性抑制 VEGF-A 與 NRP1 b1 域的結(jié)合, IC50 為 3μM,但對 VEGFA 與 VEGFR-1 和 VEGFR-2 的結(jié)合沒有影響。
靶點

IC50: 8 μM ( 125 I-VEGF-A binding to PAE/NRP1); 3 μM (bt-VEGF-A binding to purified NRP1 b1 domain).

體外研究

EG00229 (Compound 2; 0-100 μM; 48 hours; A549 cells) treatment causes a significant reduction in cell viability over a 48 hours incubation.
EG00229 (Compound 2) demonstrates inhibition of VEGF-A binding to NRP1 and attenuates VEGFR2 phosphorylation in endothelial cells. Inhibition of migration of endothelial cells is also observed in HUVECs.
EG00229 (Compound 2) selectively inhibits radiolabeled 125 I-VEGF-A binding to porcine aortic endothelial (PAE)/NRP1, but not VEGFR2-expressing cells, with an IC 50 of 8 μM. EG00229 also inhibits VEGF-A binding to lung carcinoma A549 and prostate carcinoma DU145 cells, which express NRP1, but not VEGFR1 and VEGFR2, with similar potency. Binding of VEGF-A to human umbilical vein endothelial cells (HUVECs), which express VEGFR2, VEGFR1, and NRP1, is also inhibited by EG00229 with an IC 50 of 23 μM.

Cell Viability Assay

Cell Line: A549 cells
Concentration: 0 μM, 10 μM, 30 μM, 100 μM
Incubation Time: 48 hours
Result: Caused a significant reduction in cell viability.
體內(nèi)研究

EG00229 (0-10 mg/kg; intraperitoneal injection; three times per week; for 4 weeks; NSG mice) treatment substantially reduces tumor growth and visible vascularization.

Animal Model: 6-week old female NOD scid IL2 receptor gamma chain knockout mice (NSG mice) with ECS cells
Dosage: 0 mg/kg, 10 mg/kg
Administration: Intraperitoneal injection; three times per week; for 4 weeks
Result: Reduces tumor growth and visible vascularization.
"1210945-69-9" 相關(guān)產(chǎn)品信息
1210945-69-9 1018927-63-3
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