DPTIP
CAS No. 351353-48-5
DPTIP ( —— )
产品货号. M28511 CAS No. 351353-48-5
DPTIP 是中性鞘磷脂酶 2 的有效抑制剂,IC50 值为 30 nM。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ¥587 | 有现货 |
|
| 5MG | ¥881 | 有现货 |
|
| 10MG | ¥1473 | 有现货 |
|
| 25MG | ¥2911 | 有现货 |
|
| 50MG | ¥4269 | 有现货 |
|
| 100MG | ¥5922 | 有现货 |
|
| 500MG | 获取报价 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
| 1 mL x 10 mM in DMSO | ¥946 | 有现货 |
|
生物学信息
-
产品名称DPTIP
-
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
-
产品简述DPTIP 是中性鞘磷脂酶 2 的有效抑制剂,IC50 值为 30 nM。
-
产品描述DPTIP is an effective inhibitor of neutral sphingomyelinase 2 with an IC50 value of 30 nM.(In Vitro):DPTIP (30 μM) decreases exosome release by 50% in astrocytes. DPTIP(0.03-30 μM) dose-dependently blocks EV secretion.(In Vivo):In mice, DPTIP potently (10?mg/kg; i.p.) inhibits IL-1β-induced astrocyte-derived EV release. Brain concentrations of DPTIP are above its IC50 for neutral sphingomyelinase 2 inhibition for at least 4?h after the administration of DPTIP.
-
体外实验DPTIP blocks EV secretion in a dose dependent manner (0.03-30 μM), and at 30 μM, this compound could decrease exosome release by 50% in astrocytes.
-
体内实验DPTIP potently (10?mg/kg IP) inhibits IL-1β-induced astrocyte-derived EV release. Animal Model:Mice.Dosage:10?mg/kg.Administration:IP 0.5?h prior to IL-1β striatal injection.Result:Brain concentrations of DPTIP are above its IC50 for nSMase2 inhibition for at least 4?h after compound administration.The number of astrocyte-derived EVs was reduced by 51?±?13% 2?h post IL-1β administration.
-
同义词——
-
通路Metabolic Enzyme/Protease
-
靶点Phospholipase
-
受体——
-
研究领域——
-
适应症——
化学信息
-
CAS Number351353-48-5
-
分子量378.44
-
分子式C21H18N2O3S
-
纯度>98% (HPLC)
-
溶解度In Vitro:?DMSO : 250 mg/mL (660.61 mM)
-
SMILESOC=1C(OC)=CC(=CC1OC)C2=NC(C=3C=CC=CC3)=C(N2)C=4SC=CC4
-
化学全称——
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
产品手册
关联产品
-
Rilapladib
一种有效的、选择性的口服脂蛋白相关磷脂酶 A2 (Lp-PLA2) 抑制剂,IC50 为 0.23 nM。
-
Efipladib
Efipladib (PLA 902) 是一种有效的、选择性的、口服活性的 cPLA2α 抑制剂,抑制 LTB4 的 IC50 为 20 nM。
-
VU0155069
VU0155069 (CAY10593),化合物 69 是一种选择性磷脂酶 D1 (PLD1) 抑制剂,IC50 值为 46 nM。VU0155069 (CAY10593) 在 transwell 测定中强烈抑制几种癌细胞系的侵袭性迁移。
021-51111890
购物车()
sales@molnova.cn

