Naftopidil
CAS No. 57149-07-2
Naftopidil ( Naftopidil | BM-15275 | KT-611 | BM 15275 | KT 611 | BM15275 | KT611 | Flivas )
产品货号. M15085 CAS No. 57149-07-2
Naftopidil(INN,商品名为 Flivas)是一种抗高血压化合物,可作为选择性 α1-肾上腺素受体拮抗剂或 α 阻滞剂。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 100MG | ¥138 | 有现货 |
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| 500MG | ¥293 | 有现货 |
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| 1G | ¥475 | 有现货 |
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| 1 mL x 10 mM in DMSO | ¥375 | 有现货 |
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生物学信息
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产品名称Naftopidil
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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Naftopidil(INN,商品名为 Flivas)是一种抗高血压化合物,可作为选择性 α1-肾上腺素受体拮抗剂或 α 阻滞剂。
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产品描述Naftopidil (INN, marketed under the brand name Flivas) is an antihypertensive drug which acts as a selective α1-adrenergic receptor antagonist or alpha blocker.(In Vitro):Naftopidil suppresses human prostate tumor growth by altering interactions between tumor cells and stroma.Naftopidil (10 μM for PCa cells, 0.1-10 μM for PrSC; 3 days) shows growth inhibitory effects on PCa cells and PrSC.Naftopidil (50 μM for E9 cells, 25 μM for PrSC; 48 hours) increases the level of cell-cycle regulatory protein p27 in E9 cells, but not PrSC.(In Vivo):Naftopidil (10 mg/kg; p.o; daily; for 28 days) decreases microvessel density (MVD) in E9+PrSC tumors mice model.
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体外实验Naftopidil suppresses human prostate tumor growth by altering interactions between tumor cells and stroma.Naftopidil (10 μM for PCa cells, 0.1-10 μM for PrSC; 3 days) shows growth inhibitory effects on PCa cells and PrSC.Naftopidil (50 μM for E9 cells, 25 μM for PrSC; 48 hours) increases the level of cell-cycle regulatory protein p27 in E9 cells, but not PrSC.Cell Proliferation Assay Cell Line:PCa cells, PrSC Concentration:10 μM (PCa cells); 0.1 μM, 1 μM, 10 μM (PrSC)Incubation Time:3 days Result:Exhibited growth inhibitory effects on PCa cells and PrSC in dose-dependent manners.Western Blot Analysis Cell Line:PCa cells, PrSC Concentration:50 μM (E9 cells), 25 μM (PrSC)Incubation Time:48 hours Result:Increased the level of cell-cycle regulatory protein p27 in E9 cells, but not PrSC.
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体内实验Naftopidil (10 mg/kg; p.o; daily; for 28 days) decreases microvessel density (MVD) in E9+PrSC tumors mice model. Animal Model:Male athymic mice (7-8 weeks), with E9+PrSC xenograft Dosage:10 mg/kg Administration:Oral administration, daily, for 28 days Result:Decreased tumor weights.
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同义词Naftopidil | BM-15275 | KT-611 | BM 15275 | KT 611 | BM15275 | KT611 | Flivas
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通路Endocrinology/Hormones
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靶点Adrenergic Receptor
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受体α1A-adrenergic receptor| α1B-adrenergic receptor| α1D-adrenergic receptor
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研究领域Cardiovascular Disease
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适应症——
化学信息
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CAS Number57149-07-2
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分子量392.49
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分子式C24H28N2O3
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纯度>98% (HPLC)
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溶解度DMSO: 79 mg/mL (201.27 mM)
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SMILESOC(COC1=C2C=CC=CC2=CC=C1)CN3CCN(C4=CC=CC=C4OC)CC3
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化学全称1-(4-(2-methoxyphenyl)piperazin-1-yl)-3-(naphthalen-1-yloxy)propan-2-ol
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. Sakai H, et al. Hinyokika Kiyo. 2011 Jan;57(1):7-13.
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