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ML348

Synonyms: GNF-Pf-1127
货号 T3439Cas号 899713-86-1 一键复制产品信息 纯度: 99.88%
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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

一键复制产品信息
Rating icon 很棒

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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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
现货
200 mg
¥ 6,150
现货
500 mg
¥ 9,130
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纯度: 99.87%
颜色: 白色

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
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
该溶液配制表仅适用于固体产品。对于液体产品,请根据标明的浓度或密度计算稀释方案。

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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