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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
Powder:2-8℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year
- 保质期:
Powder:2-8℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year
- 英文名:
ADH-1 Trifluoroacetate
- 库存:
现询
- 供应商:
北京索莱宝科技有限公司
- CAS号:
1135237-88-5
- 规格:
5mg
| 基本信息 | |
| CAS | No.1135237-88-5 |
| 中文名称 | ADH-1TFA盐 |
| 英文名称 | ADH-1 Trifluoroacetate |
| 别名 | ;ADH-1Peptidetrifluroacetate;ADH-1trifluroacetate;UNII-4OJ57R316O; |
| 分子式 | C24H35F3N8O8S2 |
| 分子量 | 684.71 |
| 溶解性 | Soluble in DMSO(Need ultrasonic) |
| 纯度 | ≥98% |
| 外观(性状) | White to off-white Solid |
| 储存条件 | Powder:2-8℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year |
| SMILES | C[C@H]1C(=O)N[C@H](C(=O)N[C@@H](CSSC[C@@H](C(=O)N[C@H](C(=O)N1)CC2=CN=CN2)NC(=O)C)C(=O)N)C(C)C.C(=O)(C(F)(F)F)O |
| InChIKey | RMLOJFSXNMROLS-BMLUHVGESA-N |
| InChI | InChI=1S/C22H34N8O6S2.C2HF3O2/c1-10(2)17-22(36)29-15(18(23)32)7-37-38-8-16(27-12(4)31)21(35)28-14(5-13-6-24-9-25-13)20(34)26-11(3)19(33)30-17;3-2(4,5)1(6)7/h6,9-11,14-17H,5,7-8H2,1-4H3,(H2,23,32)(H,24,25)(H,26,34)(H,27,31)(H,28,35)(H,29,36)(H,30,33);(H,6,7)/t11-,14-,15-,16-,17-;/m0./s1 |
| PubChem CID | 24203776 |
| 靶点 | N-cadherin |
| 通路 | Others |
| 背景说明 | 是选择性和竞争性的N-钙粘蛋白(N-cadherin )拮抗剂。 |
| 生物活性 | ADH-1 Trifluoroacetate 是一种 N-粘连蛋白拮抗剂,可抑制 N-粘连蛋白介导的细胞粘附。[1-3] |
| In Vitro | ADH-1 trifluoroacetate induced apoptosis in a concentration dependent and N-cadherin dependent manner in pancreatic cancer cells.[1] The cytotoxic activity has been detected in human umbilical vein endothelial cells,PC3,and Tsu-Pr1 cells,when ADH1 exposure was evaluated at 500 micromol/l or above.[2] |
| 细胞实验 | ADH-1 trifluoroacetate treatment resulted in significant reductions in tumor growth and lung metastasis in a mouse model for pancreatic cancer.[1] Combination of ADH-1 with TMZ ILI did not improve tumor response in A375 tumors. ADH-1 increased vascular permeability without effecting tumor interstitial fluid pressure,leading to increased delivery of LPAM but not TMZ.[3] |
| 数据来源文献 | [1]. Shintani Y,et al. ADH-1 suppresses N-cadherin-dependent pancreatic cancer progression. Int J Cancer. 2008 Jan 1;122(1):71-7. [2]. Li H,Price DK,et al. ADH1,an N-cadherin inhibitor,evaluated in preclinical models of angiogenesis and androgen-independent prostate cancer. Anticancer Drugs. 2007 Jun;18(5):563-8. [3]. Turley RS,et al. Targeting N-cadherin increases vascular permeability and differentially activates AKT in melanoma. Ann Surg. 2015 Feb;261(2):368-77. |
| 单位 | 瓶 |
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