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网站主页 化合物LMPTP INHIBITOR 1 HYDROCHLORIDE 化合物 LMPTP INHIBITOR 1 hydrochloride
  • 化合物 LMPTP INHIBITOR 1 hydrochloride|T4491|TargetMol

化合物 LMPTP INHIBITOR 1 hydrochloride|T4491|TargetMol

LMPTP INHIBITOR 1 hydrochloride
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上海 更新日期:2026-05-08

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产品详情:

中文名称:
化合物 LMPTP INHIBITOR 1 hydrochloride
英文名称:
LMPTP INHIBITOR 1 hydrochloride
CAS号:
2310135-38-5
品牌:
TargetMol
产地:
美国
保存条件:
Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature.
纯度规格:
99.89%
产品类别:
抑制剂
货号:
T4491

Product Introduction

Bioactivity

名称LMPTP INHIBITOR 1 hydrochloride
描述LMPTP INHIBITOR 1 hydrochloride is a selective inhibitor of low molecular weight protein tyrosine phosphatase ( LMPTP ), with an IC 50 of 0.8 μM for LMPTP-A.
细胞实验Human HepG2 cells are cultured in Eagle's Minimal Essential Medium (ATCC) containing 10% fetal bovine serum (FBS), 100 U/mL penicillin and 100 μg/mL streptomycin. The absence of Mycoplasma contamination in HepG2 cultures is confirmed using the Lonza MycoAlert Mycoplasma Detection Kit. Cells are treated with 10 μM LMPTP inhibitor 1 in serum-starvation media (0.1% FBS) overnight, following which cells are stimulated with 10 nM bovine insulin for 5 min at 37°C. For detection of IR tyrosine phosphorylation by immunoprecipitation/Western blotting, cells are lysed in radioimmunoprecipitation assay buffer containing 1 mM phenylmethylsulfonyl fluoride, 10 μg/mL aprotinin/leupeptin, 10 mM sodium orthovanadate, 5 mM sodium fluoride, and 2 mM sodium pyrophosphate, and the IR is immunoprecipitated using the anti-IRβ Ab. IR tyrosine phosphorylation of immunoprecipitates is determined by Western blotting with the anti-pIR/pIGFR-Y1162/Y1163 Ab [1].
激酶实验Phosphatase assays are performed in buffer containing 50 mM Bis-Tris, pH 6.0, 1 mM DTT and 0.01% Triton X-100 at 37°C. For assays conducted with 3-O-methylfluorescein phosphate (OMFP) as substrate, fluorescence is monitored continuously at λex = 485 and λem = 525 nm. For assays conducted with para-nitrophenyl phosphate (pNPP) as substrate, the reaction is stopped by addition of 2X reaction volume of 1 M NaOH, and absorbance is measured at 405 nm. IC50 values are determined from plots of LMPTP inhibitor 1 concentration versus percentage of enzyme activity. For inhibitor selectivity assays, each PTP is incubated with either 0.4 mM OMFP or 5 mM pNPP in the presence of 40 μM LMPTP inhibitor 1 or DMSO. Equal units of enzyme activity, comparable to the activity of 10 nM human LMPTP-A, are used. For the inhibitor reversibility assay, 50 nM human LMPTP-A is pre-incubated with 10 μM LMPTP inhibitor 1 or DMSO for 5 min. The enzyme is diluted 100X in phosphatase assay buffer containing 0.4 mM OMFP and fluorescence is measured at the indicated time points [1].
动物实验LMPTP inhibitor 1 is administered to male B6 or Acp1fl/fl albumin-Cre+ DIO mice at 0.05% w/w in high-fat diet (HFD) rodent chow. Control groups consist of male B6 or Acp1fl/fl albumin-Cre+ littermate mice administered HFD rodent chow alone. Mice are allowed food and water ad libitum and weighed daily. Randomization is not used in these experiments; rather littermate mice are assigned to treatment or control groups in a manner to maintain similar mean body weights between the 2 groups at the start of the study. Insulin-induced liver IR phosphorylation, IPGTT, and fasting insulin levels are assessed after treatment. Diabetic (displaying overnight [13 hr] fasting blood glucose levels ≥140 mg/dL) B6 DIO mice are used in experiments to assess IPGTT and fasting insulin levels [1].
体外活性LMPTP INHIBITOR 1 (hydrochloride) 是一种对低分子量蛋白质酪氨酸磷酸酶具有选择性抑制作用的抑制剂,对LMPTP-A的IC 50值为0.8 μM。LMPTP INHIBITOR 1 对LMPTP-A的抑制效果较之于LMPTP-B更为强大。LMPTP抑制剂1还在人类HepG2肝细胞中,通过胰岛素刺激后增强了HepG2 IR的磷酸化[1]。
体内活性LMPTP inhibitor 1 具有口服生物可用性,0.03% w/w 的处理约产生 680 nM 的平均血清浓度,而0.05% w/w 的处理则产生 >3 μM;该物质还能逆转肥胖小鼠的糖尿病。LMPTP inhibitor 1(0.05% w/w)抑制 LMPTP 活性,显著改善糖尿病 DIO 小鼠的葡萄糖耐受性并降低空腹胰岛素水平,但不影响体重[1]。
存储条件Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature.
溶解度DMSO : 9 mg/mL (18.71 mM), Sonication is recommended.
关键字LMPTP-A | LMPTP INHIBITOR 1 Hydrochloride
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相关库NO PAINS 化合物库
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LMPTP INHIBITOR 1 hydrochloride (1908414-82-3(free base))|TargetMol

公司简介

TargetMol Chemicals Inc. 总部位于马萨诸塞州波士顿,致力于为全球生化领域科学家的研究提供专业的产品和服务。TargetMol?品牌的客户群分布于40多个国家和地区,已发展成为全球知名的化合物库和小分子化合物研究供应商。 TargetMol?可提供160多种满足不同需求的化合物库,以及多种类型的生化试剂产品,包括12000多种抑制剂、16000多种天然产物和各类多肽、抗体、生命科学试剂盒等,此外,我们还建设有CADD(计算机辅助药物设计)研究中心、药理实验室、药化合成平台三大技术中心,全方位满足客户的定制需求。 凭借我们优质的产品和服务、快速高效的全球供应链和专业的技术支持,我们将有效帮助您缩短研发周期,取得更成功的结果。

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