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SJG-136 是一种 DNA 交联剂,对 pBR322 DNA 的 XL50 值为 45 nM。SJG-136 表现出较强抗肿瘤相关活性,并适用于 DNA 交联形成、基因组损伤应答及肿瘤相关细胞应激通路研究。
别名 SJG 136, NSC-694501, NSC 694501
SJG-136 是一种 DNA 交联剂,对 pBR322 DNA 的 XL50 值为 45 nM。SJG-136 表现出较强抗肿瘤相关活性,并适用于 DNA 交联形成、基因组损伤应答及肿瘤相关细胞应激通路研究。

| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 1 mg | ¥ 1,850 | 10-14周 | |
| 5 mg | ¥ 3,690 | 10-14周 | |
| 10 mg | ¥ 5,290 | 10-14周 | |
| 25 mg | ¥ 7,980 | 10-14周 | |
| 50 mg | ¥ 10,700 | 10-14周 | |
| 1 mL x 10 mM (in DMSO) | ¥ 4,530 | 10-14周 |
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| 产品描述 | SJG-136 is a DNA cross-linking agent with an XL50 value of 45 nM for pBR322 DNA. SJG-136 demonstrates potent antitumor activity and is applicable to investigations involving DNA cross-link formation, genomic damage responses, and tumor-associated cellular stress pathways. |
| 靶点活性 (IC₅₀) | pBR322 DNA:45 nM(XL50) |
| 体外活性 | SJG-136 对卵巢细胞系具有细胞毒性,例如 A2780(IC50:22.5 pM)、A2780cisR(IC50:24 pM)、 CH1(IC50:0.12 nM)、CH1cisR(IC50:0.6 nM)以及 SKOV-3(IC50:9.1 nM)。SJG-136 还能降低一系列犬类癌细胞的存活率(GI50:经 1 小时暴露后范围为 0.33 - >100 nM,连续暴露后为 <0.03 - 17.33 nM)[1][2]。 |
| 体内活性 | SJG-136-induced H2AX phosphorylation shows good correspondence, but less sensitivity, than measurement of foci. SJG-136 displays a more potent antitumor effect against CMeC-1 tumor at 0.30 mg/kg than 0.15 mg/kg either as a single dose or administered once a week for three weeks via dosed intravenously in mice [2]. |
| 别名 | SJG 136, NSC-694501, NSC 694501 |
| 分子量 | 556.61 |
| 分子式 | C31H32N4O6 |
| CAS No. | 232931-57-6 |
| Smiles | O=C1C=2C(=CC(OCCCOC3=C(OC)C=C4C(=C3)N=C[C@]5(N(C4=O)CC(=C)C5)[H])=C(OC)C2)N=C[C@]6(N1CC(=C)C6)[H] |
| 密度 | 1.36g/cm3 |
| 存储 | Keep away from direct sunlight,Keep away from moisture Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. 实际储存温度请以COA为准 | |||||||||||||||||||||||||
| 溶解度信息 | DMSO: 26.66 mg/mL (47.9 mM), Sonication is recommended. | |||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||
DMSO
该溶液配制表仅适用于固体产品。对于液体产品,请根据标明的浓度或密度计算稀释方案。 | ||||||||||||||||||||||||||
对于不同动物的给药剂量换算,您也可以参考 更多