ML-098结构式
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常用名 | ML-098 | 英文名 | ML-098 |
|---|---|---|---|---|
| CAS号 | 878978-76-8 | 分子量 | 309.359 | |
| 密度 | 1.2±0.1 g/cm3 | 沸点 | 535.5±45.0 °C at 760 mmHg | |
| 分子式 | C19H19NO3 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 277.7±28.7 °C |
ML-098用途ML-098(CID-7345532)是GTP结合蛋白Rab7的激活剂,EC50值为77.6nM。 |
| 中文名 | ML-098 |
|---|---|
| 英文名 | 1-[2-(2,5-Dimethylphenoxy)ethyl]-1H-indole-3-carboxylic acid |
| 英文别名 | 更多 |
| 描述 | ML-098(CID-7345532)是GTP结合蛋白Rab7的激活剂,EC50值为77.6nM。 |
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| 相关类别 | |
| 靶点实验 |
EC50: 77.6 nM (Rab7)[1] |
| 体外研究 | 探针化合物mL098(CID-7345532)通过增加GTP酶对鸟嘌呤核苷酸的亲和力起作用,导致假设这些激活剂与GTP酶相互作用,结合位于开关区I和II之间的变构结合位点。 ML-098是GTP结合蛋白Rab7的活化剂,EC50为77.6 nM,显示出对相关GTP酶cdc42,Ras,Rab-2A和Rac1的选择性(EC50s分别为588.8,346.7,158.5和794.3 nM) )[1]。 |
| 密度 | 1.2±0.1 g/cm3 |
|---|---|
| 沸点 | 535.5±45.0 °C at 760 mmHg |
| 分子式 | C19H19NO3 |
| 分子量 | 309.359 |
| 闪点 | 277.7±28.7 °C |
| 精确质量 | 309.136505 |
| PSA | 51.46000 |
| LogP | 4.96 |
| InChIKey | LILIWWFBJKBUCO-UHFFFAOYSA-N |
| SMILES | Cc1ccc(C)c(OCCn2cc(C(=O)O)c3ccccc32)c1 |
| 蒸汽压 | 0.0±1.5 mmHg at 25°C |
| 折射率 | 1.593 |
| 储存条件 | 2-8℃ |
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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:Primary qHTS assay for small molecule inhibitors of Inositol hexaphosphate kinase 1 (...
来源:NCGC
External Id:IP6K1-p1
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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
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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
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实验名称:Dose response of compounds that promote myeloid differentiation with HOXA9ER cells wi...
来源:NMMLSC
External Id:UNMCMD_HOXA9_MYELOIDDIFFERENTIATION_HOXA9ER_SAR01
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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
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实验名称:Cytochrome P450 family 3 subfamily A member 4 (CYP3A4) small molecule antagonists: lu...
来源:NCGC
External Id:CYP3A4437
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实验名称:Cytochrome P450 family 2 subfamily D member 6 (CYP2D6) small molecule antagonists: lu...
来源:NCGC
External Id:CYP2D6395
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实验名称:Cytochrome P450 family 2 subfamily C member 9 (CYP2C9) small molecule antagonists: lu...
来源:NCGC
External Id:CYP2C9536
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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.
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| 1-[2-(2,5-Dimethylphenoxy)ethyl]-1H-indole-3-carboxylic acid |
| ML-098 |