ML-030

• 常用名: ML-030
• 英文名: ML-030
• CAS号: 1013750-77-0
• 分子量: 412.462
• 密度: 1.4±0.1 g/cm3
• 沸点: 633.2±65.0 °C at 760 mmHg
• 分子式: C₂₀H₂₀N₄O₄S
• 熔点: N/A
• 闪点: 336.7±34.3 °C

ML-030用途

ML-030 是一种有效的 PDE4 抑制剂,对 PDE4A,PDE4A1,PDE4B1,PDE4B2,PDE4C1 和 PDE4D2 的 IC50 值分别为 6.7 nM,12.9 nM,48.2 nM,37.2 nM,452 nM 和 49.2 nM。

ML-030名称

• 中文名: ML-030
• 英文名: 3-(2,5-Dimethoxyphenyl)-6-(3,4-dimethoxyphenyl)-7H-[1,2,4]triazol o[3,4-b][1,3,4]thiadiazine

ML-030生物活性

• 描述: ML-030 是一种有效的 PDE4 抑制剂,对 PDE4A,PDE4A1,PDE4B1,PDE4B2,PDE4C1 和 PDE4D2 的 IC50 值分别为 6.7 nM,12.9 nM,48.2 nM,37.2 nM,452 nM 和 49.2 nM。
• 相关类别:
  信号通路 >> 代谢酶/蛋白酶 >> 磷酸二酯酶(PDE)
  研究领域 >> 炎症/免疫
• 靶点实验:

  IC50: 6.7 nM (PDE4A), 12.9 nM (PDE4A1), 48.2 nM (PDE4B1), 37.2 (PDE4B2) nM, 452 (PDE4C1) nM, 49.2 (PDE4D2) nM[1]

• 体外研究: ML-030在基于细胞的分析中有效,EC50值为18.7 nM [1]。
• 参考文献:

  [1]. Skoumbourdis AP, et al. Exploration and optimization of substituted triazolothiadiazines and triazolopyridazines as PDE4 inhibitors. Bioorg Med Chem Lett. 2009 Jul 1;19(13):3686-92.

ML-030物理化学性质

• 密度: 1.4±0.1 g/cm3
• 沸点: 633.2±65.0 °C at 760 mmHg
• 分子式: C₂₀H₂₀N₄O₄S
• 分子量: 412.462
• 闪点: 336.7±34.3 °C
• 精确质量: 412.120514
• PSA: 105.29000
• LogP: 3.56
• InChIKey: DZAUSKKPHXFGNN-UHFFFAOYSA-N
• SMILES: COc1ccc(OC)c(-c2nnc3n2N=C(c2ccc(OC)c(OC)c2)CS3)c1
• 蒸汽压: 0.0±1.9 mmHg at 25°C
• 折射率: 1.650
• 储存条件: 2-8℃

ML-030靶点实验

查看更多实验

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：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：Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect... 来源：Broad Institute 靶标：N/A External Id：Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity

实验名称：Fluorescence-based cell-based primary high throughput screening assay to identify pos... 来源：The Scripps Research Institute Molecular Screening Center 靶标：muscarinic acetylcholine receptor M1 [Homo sapiens] External Id：CHRM1_PAM_FLUO8_1536_1X%ACT PRUN

实验名称：Primary qHTS for Identification of Calcium Integrin Binding Protein 1 (CIB1) Competit... 来源：NCGC External Id：CIB1-p1-p2

实验名称：Fluorescence polarization-based biochemical high throughput primary assay to identify... 来源：The Scripps Research Institute Molecular Screening Center 靶标：RecName: Full=Sialate O-acetylesterase; AltName: Full=H-Lse; AltName: Full=Sialic acid-specific 9-O-acetylesterase; Flags: Precursor [Homo sapiens] External Id：SIAE_INH_FP_1536_1X%INH PRUN

实验名称：Absorbance-based primary biochemical high throughput screening assay to identify acti... 来源：The Scripps Research Institute Molecular Screening Center 靶标：caspase-3 preproprotein [Homo sapiens] External Id：PROCASPASE3_ACT_EPIABS_1536_1X%ACT PRUN

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ML-030英文别名

• 3-(2,5-Dimethoxyphenyl)-6-(3,4-dimethoxyphenyl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazine
• ML-030