氯苯氨啶结构式
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常用名 | 氯苯氨啶 | 英文名 | Metoprine |
|---|---|---|---|---|
| CAS号 | 7761-45-7 | 分子量 | 269.13000 | |
| 密度 | 1.447g/cm3 | 沸点 | 483.7ºC at 760 mmHg | |
| 分子式 | C11H10Cl2N4 | 熔点 | 275-276ºC | |
| MSDS | N/A | 闪点 | 246.3ºC |
氯苯氨啶用途Metoprine (BW 197U) 是一种有效的组胺 N-甲基转移酶 (HMT) 抑制剂。Metoprine 是一种二氨基嘧啶衍生物,可以透过血脑屏障,并通过抑制 HMT 增加脑组胺水平。Metoprine 是一种抗叶酸 (antifolate) 和抗肿瘤药。 |
| 中文名 | 氯苯氨啶 |
|---|---|
| 英文名 | 5-(3,4-dichlorophenyl)-6-methylpyrimidine-2,4-diamine |
| 英文别名 | 更多 |
| 描述 | Metoprine (BW 197U) 是一种有效的组胺 N-甲基转移酶 (HMT) 抑制剂。Metoprine 是一种二氨基嘧啶衍生物,可以透过血脑屏障,并通过抑制 HMT 增加脑组胺水平。Metoprine 是一种抗叶酸 (antifolate) 和抗肿瘤药。 |
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| 相关类别 | |
| 体内研究 | 美托普利(BW 197U;2-10mg/kg;IP)以剂量依赖性的方式改善基底大细胞(NBM)损伤引起的记忆障碍[2]。腹腔注射美托普利会产生各种行为效应,包括食物摄入减少和耗水量增加[1]。动物模型:雄性Sprague-dawley大鼠(200-280g)[2]剂量:2,5,10mg/kg给药:IP结果:大鼠基底核(NBM)损伤引起的记忆障碍呈剂量依赖性改善,高剂量10mg/kg可显著延长转移潜伏期。 |
| 参考文献 |
| 密度 | 1.447g/cm3 |
|---|---|
| 沸点 | 483.7ºC at 760 mmHg |
| 熔点 | 275-276ºC |
| 分子式 | C11H10Cl2N4 |
| 分子量 | 269.13000 |
| 闪点 | 246.3ºC |
| 精确质量 | 268.02800 |
| PSA | 77.82000 |
| LogP | 4.08560 |
| InChIKey | VQJHOPSWBGJHQS-UHFFFAOYSA-N |
| SMILES | Cc1nc(N)nc(N)c1-c1ccc(Cl)c(Cl)c1 |
| 折射率 | 1.678 |
| 储存条件 | 2-8°C,干燥,密封 |
| 计算化学 | 1.疏水参数计算参考值(XlogP):无 2.氢键供体数量:2 3.氢键受体数量:4 4.可旋转化学键数量:1 5.互变异构体数量:17 6.拓扑分子极性表面积:77.8 7.重原子数量:17 8.表面电荷:0 9.复杂度:266 10.同位素原子数量:0 11.确定原子立构中心数量:0 12.不确定原子立构中心数量:0 13.确定化学键立构中心数量:0 14.不确定化学键立构中心数量:0 15.共价键单元数量:1 |
| 危害码 (欧洲) | Xi |
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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
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实验名称:Primary qHTS assay for inhibitors of alpha-synuclein gene (SNCA) expression
来源:NCGC
External Id:SNCA-p-activity-luciferase
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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:Cytochrome P450 Family 1 Subfamily A Member 2 (CYP1A2) small molecule antagonists: lu...
来源:824
External Id:CYP273
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实验名称:Counterscreen for inhibitors of the Steroid Receptor Coactivator 1 (SRC1; NCOA1): Lum...
来源:The Scripps Research Institute Molecular Screening Center
靶标:transactivating tegument protein VP16 [Human herpesvirus 1]
External Id:VP16_INH_LUMI_1536_3X%INH CSRUN for SRC1
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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
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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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实验名称:Luminescence-based cell-based high throughput confirmation assay for inhibitors of th...
来源:The Scripps Research Institute Molecular Screening Center
靶标:nuclear receptor coactivator 1 isoform 1 [Homo sapiens]
External Id:SRC1_INH_LUMI_1536_3X%INH CRUN
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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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实验名称:p53 small molecule agonists, cell-based qHTS assay: qHTS cell viability counter scree...
来源:824
靶标:N/A
External Id:P53600
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| METOPRINE,METHODICHLOROPHEN |
| BW-197U |
| 2aov |
| DDMP |
| METOPRINE |
| SK 5265 |
| Methodichlorophen |