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ML-031

更新时间:2025-08-22 11:59:53

ML-031结构式
ML-031结构式
品牌特惠专场
常用名 ML-031 英文名 ML031
CAS号 852230-33-2 分子量 324.374
密度 1.2±0.1 g/cm3 沸点 568.8±50.0 °C at 760 mmHg
分子式 C19H20N2O3 熔点 N/A
MSDS N/A 闪点 297.8±30.1 °C

 ML-031用途


CYM-5482是一种有效的选择性激动剂鞘氨醇1-磷酸受体2(S1PR2),IC50和EC50分别为1.0和1.03μM。CYM-5482具有研究癌症疾病的潜力【1】。

 ML-031名称

中文名 ML-031
英文名 1-[2-(1-Benzyl-2,5-dimethyl-1H-pyrrol-3-yl)-2-oxoethyl]-2,5-pyrro lidinedione
英文别名 更多

 ML-031生物活性

描述 CYM-5482是一种有效的选择性激动剂鞘氨醇1-磷酸受体2(S1PR2),IC50和EC50分别为1.0和1.03μM。CYM-5482具有研究癌症疾病的潜力【1】。
相关类别
参考文献

[1]. Satsu H, et al. A sphingosine 1-phosphate receptor 2 selective allosteric agonist. Bioorg Med Chem. 2013;21(17):5373-5382.

 ML-031物理化学性质

密度 1.2±0.1 g/cm3
沸点 568.8±50.0 °C at 760 mmHg
分子式 C19H20N2O3
分子量 324.374
闪点 297.8±30.1 °C
精确质量 324.147400
PSA 59.38000
LogP 1.95
InChIKey JRESCQKIRPOOEM-UHFFFAOYSA-N
SMILES Cc1cc(C(=O)CN2C(=O)CCC2=O)c(C)n1Cc1ccccc1
蒸汽压 0.0±1.6 mmHg at 25°C
折射率 1.617
储存条件 -20°C,密闭,干燥

 ML-031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:A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS979
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: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
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 ML-031英文别名

1-[2-(1-Benzyl-2,5-dimethyl-1H-pyrrol-3-yl)-2-oxoethyl]-2,5-pyrrolidinedione
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