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S85659

Genz-644282

源叶(MedMol) ≥98%
  • 英文名:
  • 2,3-dimethoxy-12-(2-(methylamino)ethyl)-[1,3]dioxolo[4',5':4,5]benzo[1,2-h]benzo[c][1,6]naphthyridin-13(12H)-one
  • 别名:
  • GENZ644282; GENZ-644282; GENZ 644282; SAR402674; SAR 402674; SAR-402674.
  • CAS号:
  • 529488-28-6
  • 分子式:
  • C22H21N3O5
  • 分子量:
  • 407.42
品牌货号产品规格价格(RMB) 库存(上海) 北京 武汉 南京 数量计量单位 加入购物车...
源叶(MedMol) S85659-5mg ≥98% ¥256.00元 4 - - - EA 加入购物车
源叶(MedMol) S85659-10mg ≥98% ¥472.00元 1 - - - EA 加入购物车
源叶(MedMol) S85659-25mg ≥98% ¥1175.00元 1 - - - EA 加入购物车
源叶(MedMol) S85659-50mg ≥98% ¥2340.00元 1 - - - EA 加入购物车
源叶(MedMol) S85659-100mg ≥98% ¥4650.00元 1 - - - EA 加入购物车
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  • 提示:详情请下载说明书。
  • 产品描述: Genz-644282, a novel non-camptothecin topoisomerase I inhibitor for cancer treatment
  • 靶点: Topoisomerase
  • 体外研究:
    Human bone marrow CFU-GM was more sensitive to the Top1 inhibitors than was mouse bone marrow CFU-GM. The ratio of mouse to human IC(90) values was more than 10 for the camptothecins and less than 10 for Genz-644282, which had more potency as a cytotoxic agent toward human tumor cells in culture than the camptothecins in the colony-forming and 72-hour proliferation assays. Genz-644282 has superior or equal antitumor activity in the human tumor xenografts than the standard drug comparators
  • 体内研究:
    In vivo, Genz-644282 at its MTD (4 mg/kg) induced maintained complete responses (MCR) in 6/6 evaluable solid tumor models. At 2 mg/kg Genz-644282 induced CR or MCR in 3/3 tumor models relatively insensitive to topotecan, but there were no objective responses at 1 mg/kg. Further testing at 2 mg/kg showed that Genz-644282 induced objective regressions in 7 of 17 (41%) models. There was a significant correlation between predictive response scores based on Affymetrix U133Plus2 baseline tumor expression profiles and the observed in vivo responses to Genz-644282
  • 细胞实验: Colony-forming assays were conducted with mouse and human bone marrow and eight human tumor cell lines. In addition, 29 human tumor cell lines representing a range of histology and potential resistance mechanisms were assayed for sensitivity to Genz-644282 in a 72-hour exposure assay. The efficacy of Genz-644282 was compared with standard anticancer drugs (i.e., irinotecan, docetaxel, and dacarbazine) in human tumor xenografts of colon cancer, renal cell carcinoma, non-small cell lung cancer, and melanoma.
  • 动物实验: Genz-644282 was tested against the PPTP in vitro panel (0.1 nM to 1 μM), and in vivo using three times per week × 2 schedule repeated at day 21 at its maximum tolerated dose (MTD) of 4 mg/kg. Subsequently Genz-644282 was tested at 4, 3, 2, and 1 mg/kg in 3 models to assess the dose-response relationship. mRNA gene signatures predictive for Genz-644282 response in vitro were applied to select 15 tumor models that were evaluated prospectively.
  • 参考文献:
    1. Kurtzberg L S , Roth S , Krumbholz R , et al. Genz-644282, a Novel Non-Camptothecin Topoisomerase I Inhibitor for Cancer Treatment[J]. Clinical Cancer Research, 2011, 17(9):2777-2787. 2. Houghton P J , Lock R , Carol H , et al. Testing of the Topoisomerase 1 Inhibitor Genz644282 by the Pediatric Preclinical Testing Program[J]. Pediatric Blood & Cancer, 2012, 58(2):200-209.
  • 溶解性: Soluble  in  DMSO
  • 保存条件: -20℃
  • 配置溶液浓度参考:
    1mg 5mg 10mg
    1 mM 2.454 ml 12.272 ml 24.545 ml
    5 mM 0.491 ml 2.454 ml 4.909 ml
    10 mM 0.245 ml 1.227 ml 2.454 ml
    50 mM 0.049 ml 0.245 ml 0.491 ml
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