MAT2A-IN-12

• 常用名: MAT2A-IN-12
• 英文名: MAT2A-IN-12
• CAS号: 631897-75-1
• 分子量: 319.35
• 密度: N/A
• 沸点: N/A
• 分子式: C₂₀H₁₇NO₃
• 熔点: N/A
• 闪点: N/A

MAT2A-IN-12用途

MAT2A Allosteric inhibitor 2 是一种有效的、选择性的 MAT2A 变构抑制剂,其 IC50 为 5 nM。MAT2A Allosteric inhibitor 2 在增殖试验 (MTAP-/-细胞系) 中显示纳摩尔活性 (IC50=5 μM)。

MAT2A-IN-12名称

• 英文名: MAT2A-IN-12

MAT2A-IN-12生物活性

• 描述: MAT2A Allosteric inhibitor 2 是一种有效的、选择性的 MAT2A 变构抑制剂,其 IC50 为 5 nM。MAT2A Allosteric inhibitor 2 在增殖试验 (MTAP-/-细胞系) 中显示纳摩尔活性 (IC50=5 μM)。
• 相关类别:
  研究领域 >> 癌症
• 参考文献:

  [1]. Tuomo Kalliokoski, et al. Discovery of novel methionine adenosyltransferase 2A (MAT2A) allosteric inhibitors by structure-based virtual screening. Bioorg Med Chem Lett . 2023 Oct 1;94:129450

MAT2A-IN-12物理化学性质

• 分子式: C₂₀H₁₇NO₃
• 分子量: 319.35
• InChIKey: BWMRZPZVODSGTH-UHFFFAOYSA-N
• SMILES: COc1ccc2oc3cc(C)[n+]([O-])c(-c4ccc(C)cc4)c3c2c1

MAT2A-IN-12靶点实验

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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

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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：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：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

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