SB756050结构式
|
常用名 | SB756050 | 英文名 | SB756050 |
|---|---|---|---|---|
| CAS号 | 447410-57-3 | 分子量 | 500.586 | |
| 密度 | 1.3±0.1 g/cm3 | 沸点 | 653.1±65.0 °C at 760 mmHg | |
| 分子式 | C21H28N2O8S2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 348.8±34.3 °C |
SB756050用途SB756050是选择性的 TGR5 激动剂,目前正处于临床一期实验用于治疗二型糖尿病。 |
| 中文名 | SB756050 |
|---|---|
| 英文名 | SB756050 |
| 英文别名 | 更多 |
| 描述 | SB756050是选择性的 TGR5 激动剂,目前正处于临床一期实验用于治疗二型糖尿病。 |
|---|---|
| 相关类别 | |
| 体外研究 | TGR5是一种胆汁酸受体,是治疗2型糖尿病(T2D)的潜在靶点[1]。 |
| 体内研究 | SB756050耐受性良好;它易于吸收,表现出非线性药代动力学,血浆暴露量高于100mg时剂量成比例增加小于1mg,并且当与西他列汀共同给药时,暴露没有显着变化。 SB756050在剂量组和剂量之间表现出高度可变的药效学效应,在两个最低剂量下观察到葡萄糖增加,并且在两个最高剂量下观察到葡萄糖没有减少。 SB756050þ西他列汀的葡萄糖效应与单独的西他列汀相当,即使肠激素血浆谱不同[1]。 |
| 参考文献 |
| 密度 | 1.3±0.1 g/cm3 |
|---|---|
| 沸点 | 653.1±65.0 °C at 760 mmHg |
| 分子式 | C21H28N2O8S2 |
| 分子量 | 500.586 |
| 闪点 | 348.8±34.3 °C |
| 精确质量 | 500.128693 |
| LogP | 4.70 |
| InChIKey | GJUFPAZNBPFNRI-UHFFFAOYSA-N |
| SMILES | COc1ccc(S(=O)(=O)N2CCCN(S(=O)(=O)c3ccc(OC)c(OC)c3)CC2)cc1OC |
| 外观性状 | white solid |
| 蒸汽压 | 0.0±2.0 mmHg at 25°C |
| 折射率 | 1.569 |
| 储存条件 | 室温 |
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实验名称:Screen for inhibitors of RMI FANCM (MM2) intereaction
来源:11908
靶标:N/A
External Id:RMI-FANCM-MM2
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实验名称:Antiviral activity determined as inhibition of SARS-CoV-2 induced cytotoxicity of VER...
来源:ChEMBL
靶标:Severe acute respiratory syndrome coronavirus 2
External Id:CHEMBL4513082
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实验名称:Antiviral activity determined as inhibition of SARS-CoV-2 induced cytotoxicity of Cac...
来源:ChEMBL
靶标:Severe acute respiratory syndrome coronavirus 2
External Id:CHEMBL4303805
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实验名称:Cell-based high throughput primary assay to identify activators of GPR151
来源:The Scripps Research Institute Molecular Screening Center
靶标:RecName: Full=G-protein coupled receptor 151; AltName: Full=G-protein coupled receptor PGR7; AltName: Full=GPCR-2037; AltName: Full=Galanin receptor 4; AltName: Full=Galanin-receptor-like protein; Short=GalRL
External Id:GPR151_PHUNTER_AG_LUMI_1536_1X%ACT
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实验名称:SARS-CoV-2 3CL-Pro protease inhibition percentage at 20µM by FRET kind of response f...
来源:ChEMBL
靶标:Replicase polyprotein 1ab
External Id:CHEMBL4495582
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实验名称:Discovering small molecule activators of G protein-gated inwardly-rectifying potassiu...
来源:15621
靶标:G protein-activated inward rectifier potassium channel 2
External Id:VANDERBILT_HTS_GIRK2_MPD
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实验名称:Enzymatic assay of human HDAC6 with commercial peptide substrate
来源:ChEMBL
靶标:Histone deacetylase 6
External Id:CHEMBL4808149
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实验名称:Enzymatic assay of human HDAC6 with custom peptide substrate
来源:ChEMBL
靶标:Histone deacetylase 6
External Id:CHEMBL4808150
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实验名称:Agonist activity at human TGR5
来源:ChEMBL
靶标:G-protein coupled bile acid receptor 1
External Id:CHEMBL5247724
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实验名称:High-throughput screen for inhibitors of the GIV GBA-motif interaction with Galpha-i ...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS1303
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| MFCD02585318 |
| 1,4-Bis[(3,4-dimethoxyphenyl)sulfonyl]-1,4-diazepane |