DX-8951衍生物
- CAS号:1599440-33-1
- 英文名:Dxd
- 中文名:DX-8951衍生物
- CBNumber:CB74796647
- 分子式:C26H24FN3O6
- 分子量:493.48
- MOL File:1599440-33-1.mol
- 沸点 :957.9±65.0 °C(Predicted)
- 密度 :1.57±0.1 g/cm3(Predicted)
- 储存条件 :Store at -20°C
- 溶解度 :DMSO:40.0(Max Conc. mg/mL);81.06(Max Conc. mM)
- 形态 :Solid
- 酸度系数(pKa) :11.18±0.40(Predicted)
DX-8951衍生物性质、用途与生产工艺
- 生物活性 Dxd (Exatecan derivative for ADC) 是一种有效的 DNA topoisomerase I 抑制剂,IC50 值为 0.31 μM,可用作靶作用于 HER2 的 抗体偶联药物 ADC (DS-8201a) 的有效载荷。
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靶点
Topoisomerase I
0.31 μM (IC 50 )
Camptothecins
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体外研究
Dxd (Exatecan derivative for ADC) is a potent DNA topoisomerase I inhibitor, with an IC 50 of 0.31 μM, used as a conjugated drug of HER2-targeting ADC (DS-8201a). Dxd is cytotoxic to human cancer cell lines of KPL-4, NCI-N87, SK-BR-3, and MDA-MB-468 with IC 50 s of 1.43 nM-4.07 nM, but the control IgG-ADC (Dxd is the payload) shows no inhibition on the four cell lines (with HER2 expression). DS-8201a (Dxd is the payload) displays significant suppression on the HER2-positive KPL-4, NCI-N87, and SK-BR-3 cell lines, with IC 50 values of 26.8, 25.4, and 6.7 ng/mL, respectively, but with no such inhibition on MDA-MB-468 (IC 50 , >10,000 ng/mL).
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体内研究
DS-8201a (Dxd is the payload, 10 mg/kg, i.v.) shows potent antitumor activity in HER2-positive models with KPL4, JIMT-1, and Capan-1 and in HER2 low-expressing ST565 and ST313 models with HER2 IHC 1+/FISH-negative expression.
- 更新日期:2024/11/08
- 产品编号:HY-13631D
- 产品名称:Dxd
- CAS编号:
- 包装:1 mg
- 价格:1142元
- 更新日期:2024/11/08
- 产品编号:HY-13631D
- 产品名称:DX-8951衍生物 Dxd
- CAS编号:1599440-33-1
- 包装:5mg
- 价格:1400元
- 公司名称:BTC pharm India
- 联系电话: +918790379245
- 电子邮件:banny.janga@btcpharm.com
- 国家:印度
- 产品数:1262
- 优势度:58