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ML348

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纯度: 99.88%

货号 T3439Cas号 899713-86-1

别名 GNF-Pf-1127

ML348 (GNF-Pf-1127) 是一个选择性的、可逆的酰基蛋白硫酯酶 1 (APT1)/溶血磷脂酶 1 (LYPLA1) 抑制剂,IC50=210 nM。

ML348
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ML348

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Rating icon 很棒

纯度: 99.88%

货号 T3439 别名 GNF-Pf-1127Cas号 899713-86-1

ML348 (GNF-Pf-1127) 是一个选择性的、可逆的酰基蛋白硫酯酶 1 (APT1)/溶血磷脂酶 1 (LYPLA1) 抑制剂,IC50=210 nM。

规格价格库存数量
1 mg
¥ 258
现货
2 mg
¥ 378
现货
5 mg
¥ 647
现货
10 mg
¥ 955
现货
25 mg
¥ 1,980
现货
50 mg
¥ 2,950
现货
100 mg
¥ 4,350
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200 mg
¥ 6,150
现货
500 mg
¥ 9,130
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产品介绍


ML348 AI Summary
ML348 demonstrates a variety of biological activities and potencies across different assays. It shows moderate inhibition of Plasmodium falciparum 3D7 (drug-susceptible) with an EC50 value of 4040.0 nM but has no significant effect on the drug-resistant W2 strain. It exhibits substantial cytotoxicity against the human hepatocellular carcinoma cell line Huh7 with a CC50 value greater than 100000.0 nM and does not induce or inhibit activity in the Inhibition Frequency Index (IFI) assay. The compound acts as a delayed death inhibitor of the malarial parasite plastid with a potency of 1651.1 nM, and enhances SMN2 splice variant expression with a potency of 14125.4 nM. It inhibits multiple targets including Cruzain (39810.7 nM), ALDH1A1 (39810.7 nM), ELG1-dependent DNA repair in HEK293T cells (29092.9 nM), and human tyrosyl-DNA phosphodiesterase 1 (TDP1) with potencies of 23109.3 nM (absence of CPT) and 20596.2 nM (presence of CPT). It exhibits lower potencies as an agonist of gsp (50118.7 nM) and inhibitor of the HIV-1 protein Vpr (63095.7 nM). Notably, 585472 inhibits APT1 with a Ki of 300.0 nM but shows no significant inhibition of APT2 (Ki > 10000.0 nM). With regards to antiviral activities, ML348 shows inhibition of SARS-CoV-2 induced cytotoxicity in Caco-2 cells with a mild inhibition of -1.38% at 10 µM after 48 hours. It also exhibits SARS-CoV-2 3CL-Pro protease inhibition, achieving 7.63% and 13.55% inhibition at 20 µM. Additionally, it demonstrates varying levels of inhibition against SARS-CoV-2 cytotoxicity in VERO-6 cells. In enzymatic assays, the compound shows inhibitory action on human HDAC6, with inhibition percentages of 18.28% for a commercial peptide substrate and 6.92% for a custom peptide substrate. ML348 presents a broad spectrum of biological activities with potential implications in antimalarial, antiviral, and cancer therapeutic research..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
ML348 (GNF-Pf-1127) is a selective and reversible lysophospholipase 1 (LYPLA1) inhibitor (IC50 = 210 nM).
靶点活性
LYPLA1:210 nM
别名GNF-Pf-1127
化学信息
分子量415.79
分子式C18H17ClF3N3O3
CAS No.899713-86-1
SmilesFC(F)(F)c1ccc(Cl)c(NC(=O)CN2CCN(CC2)C(=O)c2ccco2)c1
密度1.422 g/cm3 (Predicted)
储存&溶解度
存储In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
溶解度信息
DMSO: 83.33 mg/mL (200.41 mM), Sonication is recommended.
体内实验配方
10% DMSO+90% Corn Oil: 3.3 mg/mL (7.94 mM), Sonication is recommended.
请按顺序添加溶剂,在添加下一种溶剂之前,尽可能使溶液澄清。如有必要,可通过加热、超声、涡旋处理进行溶解。工作液建议现配现用。以上配方仅供参考,体内配方并不是绝对的,请根据不同情况进行调整。
溶液配制表
DMSO
1mg5mg10mg50mg
1 mM2.4051 mL12.0253 mL24.0506 mL120.2530 mL
5 mM0.4810 mL2.4051 mL4.8101 mL24.0506 mL
10 mM0.2405 mL1.2025 mL2.4051 mL12.0253 mL
20 mM0.1203 mL0.6013 mL1.2025 mL6.0127 mL
50 mM0.0481 mL0.2405 mL0.4810 mL2.4051 mL
100 mM0.0241 mL0.1203 mL0.2405 mL1.2025 mL

计算器

  • 摩尔浓度 计算器
  • 稀释 计算器
  • 配液 计算器
  • 分子量 计算器

体内实验配液计算器

请在以下方框中输入您的动物实验信息后点击计算,可以得到母液配置方法和体内配方的制备方法:
比如您的给药剂量是10 mg/kg,每只动物体重20 g,给药体积100 μL, 一共给药动物10只,您使用的配方为 10% DMSO + 40% PEG300 + 5% Tween 80 + 45% Saline / PBS / ddH2O, 那么您的工作液浓度为2 mg/mL
母液配置方法:2 mg 药物溶于 100 μL DMSO ( 母液浓度为 20 mg/mL ), 如您需要配置的浓度超过该产品的溶解度,请先与我们联系。
体内配方的制备方法:100 μL DMSO 母液, 添加 400 μL PEG300 混匀澄清, 再加 50 μL Tween 80, 混匀澄清, 再加 450 μL Saline / PBS / ddH2O 混匀澄清
以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。
方案所需的各类助溶剂如: DMSOPEG300PEG400Tween 80SBE-β-CD玉米油等, 均可在TargetMol网站点击购买。
1 请输入动物实验的基本信息
mg/kg
g
μL
2 请输入动物体内配方组成,不同的产品配方组成不同,如有配方需求,可先联系我们提供正确的体内配方。
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

剂量转换

对于不同动物的给药剂量换算,您也可以参考 更多

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