NM-3(异香豆素) T33701
品牌 | 厂商性质 | 产地 | 货期 |
---|---|---|---|
TargetMol | 生产商 | 美国 | 现货 |
性能特点
生化试剂,可用于动物细胞实验
规格 | CAS号 | 价格 | 操作 |
---|---|---|---|
500 mg | 181427-78-1 | ¥27,800.00 | 询底价 |
1 mL | 181427-78-1 | ¥2,930.00 | 询底价 |
100 mg | 181427-78-1 | ¥13,800.00 | 询底价 |
1 mg | 181427-78-1 | ¥1,330.00 | 询底价 |
50 mg | 181427-78-1 | ¥9,870.00 | 询底价 |
5 mg | 181427-78-1 | ¥3,330.00 | 询底价 |
10 mg | 181427-78-1 | ¥4,850.00 | 询底价 |
25 mg | 181427-78-1 | ¥7,630.00 | 询底价 |
Product Introduction
Bioactivity
英文名: NM-3
描述: NM-3 是一种可口服的抗血管生成的抑制剂,具有抗肿瘤活性。NM-3在体外和体内可当作辐射调节剂使用。NM-3抑制血管内皮生长因子(VEGF),从而抑制内皮细胞的增殖。NM-3与活性氧的机制诱导细胞凋亡有关。
体外活性: NM-3(100 ng/ml)对人脐静脉内皮细胞(HUVECs)具有细胞毒性,但在克隆存活实验中,对Lewis肺癌细胞(LLC)和食管腺癌细胞Seg-1(1,000 ng/ml;4h)则无此作用。[1]
体内活性: C57BL/6 female mice bearing LLC tumors were given injections for 4 consecutive days with NM-3 (25 mg/kg/day) and treated with IR (20 Gy) for 2 consecutive days. Combined treatment with NM-3 and IR significantly reduced mean tumor volume compared with either treatment alone. An increase in local tumor control was also observed in LLC tumors in mice receiving NM-3/IR therapy. When athymic nude mice bearing Seg-1 tumor xenografts were treated with NM-3 (100 mg/kg/day for 4 days) and 20 Gy (four 5 Gy fractions), significant tumor regression was observed after combined treatment (NM-3 and IR) compared with IR alone. Importantly, no increase in systemic or local tissue toxicity was observed after combined treatment (NM-3 and IR) when compared with IR alone. The bioavailability and nontoxic profile of NM-3 suggests that the efficacy of this agent should be tested in clinical radiotherapy.[1]
存储条件: Powder: -20°C for 3 years | In solvent: -80°C for 1 year
溶解度: DMSO : 27.5 mg/mL (104.08 mM)
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相关库: Mitochondria-Targeted Compound Library | Anti-Cancer Compound Library | NF-κB Signaling Compound Library | Bioactive Compounds Library Max | Inhibitor Library | Anti-Cancer Active Compound Library | Bioactive Compound Library
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注:该产品未在中华人民共和国食品药品监督管理部门申请医疗器械注册和备案,不可用于临床诊断或治疗等相关用途