Enpp/Carbonic?anhydrase-IN-2
CAS No. 2883495-39-2
Enpp/Carbonic?anhydrase-IN-2 ( —— )
产品货号. M37002 CAS No. 2883495-39-2
Enpp/Carbonic anhydrase-IN-2 (compound 1i) 是一种有效的 Enpp 和 carbonic anhydrase 抑制剂,对 NPP1、NPP2、NPP3、CA-IX, CA-XII 的 IC50 值分别 1.13、 1.07、 0.74、 0.33、 0.68。Enpp/Carbonic anhydrase-IN-2 对癌细胞具有抗增殖活性,对正常细胞具有低细胞毒性。Enpp/Carbonic anhydrase-IN-2 诱导细胞凋亡 (Apoptosis)。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥924 | 有现货 |
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| 10MG | ¥1482 | 有现货 |
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| 25MG | ¥2297 | 有现货 |
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| 50MG | ¥3069 | 有现货 |
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| 100MG | ¥4077 | 有现货 |
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| 200MG | ¥5508 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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| 1 mL x 10 mM in DMSO | ¥960 | 有现货 |
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生物学信息
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产品名称Enpp/Carbonic?anhydrase-IN-2
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述Enpp/Carbonic anhydrase-IN-2 (compound 1i) 是一种有效的 Enpp 和 carbonic anhydrase 抑制剂,对 NPP1、NPP2、NPP3、CA-IX, CA-XII 的 IC50 值分别 1.13、 1.07、 0.74、 0.33、 0.68。Enpp/Carbonic anhydrase-IN-2 对癌细胞具有抗增殖活性,对正常细胞具有低细胞毒性。Enpp/Carbonic anhydrase-IN-2 诱导细胞凋亡 (Apoptosis)。
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产品描述Enpp/Carbonic anhydrase-IN-2 (compound 1i) is a potent Enpp and carbonic anhydrase inhibitor with IC50s of 1.13, 1.07, 0.74, 0.33, 0.68 for NPP1, NPP2, NPP3, CA-IX, CA-XII respectively. Enpp/Carbonic anhydrase-IN-2 shows antiproliferative activity for cancer cells and low cytotoxic against normal cells. Enpp/Carbonic anhydrase-IN-2 induces Apoptosis.
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体外实验Enpp/Carbonic anhydrase-IN-2 (compound 1i) (0-100 μM; ) inhibits some cancer cells growth with IC50s of 0.58, 0.58, 0.63, 0.42, 0.20, 0.72, 0.41, 0.76, 0.94, 0.28, 0.49, 0.59, 0.83 μM for K-562, COLO 205, HCT-116, HCT-15, HT29, KM12, SW-620, SF-539, NCI/ADR-RES, A498, PC-3, MCF7, T-47D cells, respectively.Enpp/Carbonic anhydrase-IN-2 (0-2 μM) shows low cytotoxic against normal breast epithelial cells (HME1) and normal skin fibroblast cells (F180) with IC50s of > 50 μM.Enpp/Carbonic anhydrase-IN-2 (0.58, 1.16 μM) induces apoptosis in a dose-dependent manner at K-562 cells.Cell Proliferation Assay Cell Line:K-562, COLO 205, HCT-116, HCT-15, HT29, KM12, SW-620, SF-539, NCI/ADR-RES, A498, PC-3, MCF7, T-47D cells Concentration:0-100 μM Incubation Time:Result:Inhibited the cell growth with IC50s of 0.58, 0.58, 0.63, 0.42, 0.20, 0.72, 0.41, 0.76, 0.94, 0.28, 0.49, 0.59, 0.83 μM for K-562, COLO 205, HCT-116, HCT-15, HT29, KM12, SW-620, SF-539, NCI/ADR-RES, A498, PC-3, MCF7, T-47D cells, respectively.Apoptosis Analysis Cell Line:K-562 cells Concentration:0.58, 1.16 μM Incubation Time:Result:Induced apoptosis in a dose-dependent manner.
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体内实验——
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同义词——
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通路Membrane Transporter/Ion Channel
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靶点Carbonic Anhydrase
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受体Carbonic Anhydrase | Apoptosis | PDE
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研究领域——
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适应症——
化学信息
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CAS Number2883495-39-2
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分子量429.5
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分子式C23H24FNO4S
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO 中的溶解度 : 100 mg/mL (232.83 mM; 超声助溶 )
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SMILESC(NC1=CC=C(OS(=O)(=O)C2=CC=C(F)C=C2)C=C1)(=O)C34CC5CC(C3)CC(C4)C5
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Afnan I.Shahin, et al. Design and synthesis of new adamantyl derivatives as promising antiproliferative agents. European Journal of Medicinal Chemistry, 2022.
产品手册
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