Lalistat 1

• 常用名: Lalistat 1
• 英文名: Lalistat 1
• CAS号: 501104-16-1
• 分子量: 298.36
• 密度: N/A
• 沸点: N/A
• 分子式: C₁₂H₁₈N₄O₃S
• 熔点: N/A
• 闪点: N/A

Lalistat 1用途

Lalistat 1 是一种有效的、选择性的、竞争性的溶酶体酸性脂肪酶抑制剂,其 IC50 为 68 nM。Lalistat 1 是流感病毒的免疫球蛋白 A1 蛋白酶 (IgA1P)  的抑制剂,对其他丝氨酸水解酶,如胰蛋白酶或内酰胺酶等影响较小。Lalistat 1 可用于 C 型尼曼氏病 (NPC) 的相关研究。

Lalistat 1名称

• 英文名: Lalistat 1

Lalistat 1生物活性

• 描述: Lalistat 1 是一种有效的、选择性的、竞争性的溶酶体酸性脂肪酶抑制剂,其 IC50 为 68 nM。Lalistat 1 是流感病毒的免疫球蛋白 A1 蛋白酶 (IgA1P) 的抑制剂,对其他丝氨酸水解酶,如胰蛋白酶或内酰胺酶等影响较小。Lalistat 1 可用于 C 型尼曼氏病 (NPC) 的相关研究。
• 相关类别:
  研究领域 >> 感染
  研究领域 >> 神经疾病
  信号通路 >> 抗感染 >> 细菌
• 靶点实验:

  IC50: 68 nM ( human LAL)[1]

• 体外研究: 在Elisa试验中,Lalistat 1(0-100μM)对临床分离株的不同非分型流感嗜血杆菌(NTHi)IgAP变体具有活性。它显示了对IgA1P B1和B2的剂量依赖性抑制,但在较高的抑制剂浓度下,与这些变体的高表达水平一致。在50μM处观察到几乎完全抑制IgA1P B1和B2,在100μM处完全抑制[1]。
• 参考文献:

  [1]. Anton I Rosenbaum , et al. Thiadiazole carbamates: potent inhibitors of lysosomal acid lipase and potential Niemann-Pick type C disease therapeutics. J Med Chem . 2010 Jul 22;53(14):5281-9.

  [2]. Livia Shehaj, et al. Small-Molecule Inhibitors of Haemophilus influenzae IgA1 Protease.ACS Infect Dis. 2019 Jul 12;5(7):1129-1138.

Lalistat 1物理化学性质

• 分子式: C₁₂H₁₈N₄O₃S
• 分子量: 298.36
• InChIKey: XAWUWPUYJUOUOF-UHFFFAOYSA-N
• SMILES: O=C(Oc1nsnc1N1CCCCC1)N1CCOCC1
• 储存条件: -20°C，干燥，密封

Lalistat 1安全信息

• 危害码 (欧洲): Xi

Lalistat 1靶点实验

查看更多实验

实验名称：Primary cell-based high-throughput screening assay for identification of compounds th... 来源：Johns Hopkins Ion Channel Center 靶标：regulator of G-protein signaling 4 isoform 2 [Homo sapiens] External Id：JHICC_RGS_Act_HTS

实验名称：Luminescence-based cell-based primary high throughput screening assay to identify ago... 来源：The Scripps Research Institute Molecular Screening Center 靶标：mu-type opioid receptor isoform MOR-1 [Homo sapiens] External Id：OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN

实验名称：QFRET-based biochemical primary high throughput screening assay to identify exosite i... 来源：The Scripps Research Institute Molecular Screening Center 靶标：disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens] External Id：ADAM17_INH_QFRET_1536_1X%INH PRUN

实验名称：Fluorescence-based cell-based primary high throughput screening assay to identify ago... 来源：The Scripps Research Institute Molecular Screening Center 靶标：muscarinic acetylcholine receptor M1 [Homo sapiens] External Id：CHRM1_AG_FLUO8_1536_1X%ACT PRUN

实验名称：uHTS identification of small molecule activators of the adaptive arm of the Unfolded ... 来源：Burnham Center for Chemical Genomics 靶标：N/A External Id：BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay

实验名称：High throughput fluorescence intensity-based biochemical assay to screen for small mo... 来源：University of Pittsburgh Molecular Library Screening Center 靶标：furin (paired basic amino acid cleaving enzyme), isoform CRA_a [Homo sapiens] External Id：MH080376 Biochemical HTS for Inhibitors of the Proprotein Convertase Furin.

实验名称：Fluorescence polarization to screen for inhibitor that competite the binding of FadD2... 来源：Broad Institute 靶标：FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE) External Id：2147-01_Inhibitor_SinglePoint_HTS_Activity

实验名称：Primary Screen Inhibitors of CD40 Signaling in BL2 Cells Measured in Cell-Based Syste... 来源：Broad Institute 靶标：N/A External Id：7124-01_Inhibitor_SinglePoint_HTS_Activity

实验名称：Dicer-mediated maturation of pre-microRNA 来源：Center for Chemical Genomics, University of Michigan 靶标：N/A External Id：TargetID_659_CEMA

实验名称：A screen for small molecules that modulate mitochondrial supercomplex formation 来源：ICCB-Longwood/NSRB Screening Facility, Harvard Medical School 靶标：N/A External Id：HMS1482

共128条，当前第1页，共13页

1

2

3

4

5