产品
编 号：F465080
分子式：C21H23N3O4S
分子量：413.49
分子式：C21H23N3O4S
分子量：413.49
产品类型
规格
价格
是否有货
10mM*1mL in DMSO
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2mg
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5mg
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10mg
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50mg
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100mg
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结构图
CAS No: 803712-79-0
产品详情
生物活性：
Obatoclax Mesylate (GX15-070 Mesylate), a BH3 mimetic, is a pan-BCL-2 family proteins inhibitor with a Ki of 220 nM for BCL-2. Obatoclax Mesylate induces autophagy-dependent cell death and targets cyclin D1 for proteasomal degradation. Obatoclax Mesylate has anti-cancer and broad-spectrum antiparasitic activity.
体内研究：
Obatoclax Mesylate (GX15-070 Mesylate; 1.15-5 mg/kg; intravenously injected; five consecutive days) exhibits potent antitumor activity in xenograft mouse models in a dose-dependent manner. Animal Model:6-8 weeks old female BALB/C nude mice bearing subcutaneous tumors
Dosage:1.15, 2.5, 5 mg/kg
Administration:Intravenously injected (through lateral tail vein); five consecutive days (i.e. 5 injections)
Result:Exhibited potent antitumor activity in xenograft mouse models in a dose-dependent manner.
体外研究：
Obatoclax Mesylate (GX15-070 Mesylate) inhibits BCL-2, BCL-XL, MCL-1, BCL-w, A1, and BCL-b with Ki values≈1-7 μM. ?Obatoclax Mesylate (50-200 nM; 24-72 hours) induces a dose- and time-dependent reduction of cell numbers in all human colorectal cancer cell lines. In particular, the IC50 of cell proliferation at 72 h are 25.85, 40.69, and 40.01 nM for HCT116, HT-29, and LoVo cells, respectively. ?Obatoclax Mesylate (400 nM; for 24 hours) induces autophagy in OSCC cells. ?Obatoclax Mesylate (50-200 nM; for 24 hours) provokes a dose-dependent increase in the G1-phase cell populations.?Obatoclax Mesylate (25-200 nM; for 24 hours) indicates a marked drop in cyclin D1 levels as low as 50 nM.?Obatoclax Mesylate induces T286 phosphorylation-dependent or -independent cyclin D1 degradation.?in HCT116 and LoVo cells, the steady-state levels of p-Cyclin D (T286) began to decline once exposed to obatoclax Mesylate (200 nM; 1, 3, 6, 12, 24 hours). Obatoclax Mesylate inhibits GSK3β but activates p38MAPK, while barely affecting ERK1/2 activity in HT-29 cells. ?Obatoclax Mesylate (50-450 nM) potently inhibits the clonogenic potential of oral cancer cells.
Obatoclax Mesylate (GX15-070 Mesylate), a BH3 mimetic, is a pan-BCL-2 family proteins inhibitor with a Ki of 220 nM for BCL-2. Obatoclax Mesylate induces autophagy-dependent cell death and targets cyclin D1 for proteasomal degradation. Obatoclax Mesylate has anti-cancer and broad-spectrum antiparasitic activity.
体内研究：
Obatoclax Mesylate (GX15-070 Mesylate; 1.15-5 mg/kg; intravenously injected; five consecutive days) exhibits potent antitumor activity in xenograft mouse models in a dose-dependent manner. Animal Model:6-8 weeks old female BALB/C nude mice bearing subcutaneous tumors
Dosage:1.15, 2.5, 5 mg/kg
Administration:Intravenously injected (through lateral tail vein); five consecutive days (i.e. 5 injections)
Result:Exhibited potent antitumor activity in xenograft mouse models in a dose-dependent manner.
体外研究：
Obatoclax Mesylate (GX15-070 Mesylate) inhibits BCL-2, BCL-XL, MCL-1, BCL-w, A1, and BCL-b with Ki values≈1-7 μM. ?Obatoclax Mesylate (50-200 nM; 24-72 hours) induces a dose- and time-dependent reduction of cell numbers in all human colorectal cancer cell lines. In particular, the IC50 of cell proliferation at 72 h are 25.85, 40.69, and 40.01 nM for HCT116, HT-29, and LoVo cells, respectively. ?Obatoclax Mesylate (400 nM; for 24 hours) induces autophagy in OSCC cells. ?Obatoclax Mesylate (50-200 nM; for 24 hours) provokes a dose-dependent increase in the G1-phase cell populations.?Obatoclax Mesylate (25-200 nM; for 24 hours) indicates a marked drop in cyclin D1 levels as low as 50 nM.?Obatoclax Mesylate induces T286 phosphorylation-dependent or -independent cyclin D1 degradation.?in HCT116 and LoVo cells, the steady-state levels of p-Cyclin D (T286) began to decline once exposed to obatoclax Mesylate (200 nM; 1, 3, 6, 12, 24 hours). Obatoclax Mesylate inhibits GSK3β but activates p38MAPK, while barely affecting ERK1/2 activity in HT-29 cells. ?Obatoclax Mesylate (50-450 nM) potently inhibits the clonogenic potential of oral cancer cells.
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