5-甲基尿嘧啶结构式
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常用名 | 5-甲基尿嘧啶 | 英文名 | 5-Methylurapidil |
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| CAS号 | 34661-85-3 | 分子量 | 437.96300 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C21H32ClN5O3 | 熔点 | N/A | |
| MSDS | 美版 | 闪点 | N/A |
5-甲基尿嘧啶用途5-Methylurapidil 是α1A-肾上腺素受体拮抗剂。5-Methylurapidil 可用于高血压、心力衰竭等心血管疾病的研究。 |
| 中文名 | 5-甲基尿嘧啶 |
|---|---|
| 英文名 | 6-[3-[4-(2-methoxyphenyl)piperazin-1-yl]propylamino]-1,3,5-trimethylpyrimidine-2,4-dione,hydrochloride |
| 英文别名 | 更多 |
| 描述 | 5-Methylurapidil 是α1A-肾上腺素受体拮抗剂。5-Methylurapidil 可用于高血压、心力衰竭等心血管疾病的研究。 |
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| 参考文献 |
| 分子式 | C21H32ClN5O3 |
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| 分子量 | 437.96300 |
| 精确质量 | 437.21900 |
| PSA | 71.74000 |
| LogP | 1.90310 |
| InChIKey | HIHZDNKKIUQQSC-UHFFFAOYSA-N |
| SMILES | COc1ccccc1N1CCN(CCCNc2c(C)c(=O)n(C)c(=O)n2C)CC1 |
| 个人防护装备 | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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| 危险品运输编码 | NONH for all modes of transport |
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Cell membrane chromatography competitive binding analysis for characterization of α1A adrenoreceptor binding interactions.
Anal. Bioanal. Chem 400(10) , 3625-33, (2011) A new high α(1A) adrenoreceptor (α(1A)AR) expression cell membrane chromatography (CMC) method was developed for characterization of α(1A)AR binding interactions. HEK293 α(1A) cell line, which express... |
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Influence of high dietary sodium intake on the functional subtypes of alpha-adrenoceptors in the renal cortical vasculature of Wistar-Kyoto rats.
Auton. Autacoid Pharmacol. 29(1-2) , 25-31, (2009) 1 Increased renal vascular resistance is one renal functional abnormality that contributes to hypertension, and alpha(1)-adrenoceptors play a pivotal role in modulating this renal vascular resistance.... |
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Alpha-1A adrenergic receptor activation increases inhibitory tone in CA1 hippocampus.
Epilepsy Res. 84(2-3) , 97-109, (2009) The endogenous catecholamine norepinephrine (NE) exhibits anti-epileptic properties, however it is not well understood which adrenergic receptor (AR) mediates this effect. The aim of this study was to... |
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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:qHTS to identify inhibitors of the New Delhi Metallo-beta-lactamase (NDM): assay vali...
来源:NCGC
External Id:adst_MBL_Abs_LOPAC_o1
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实验名称:Primary qHTS for small molecule stabilizers of the endoplasmic reticulum resident pro...
来源:NCGC
靶标:N/A
External Id:SERCaMPGLuc-p1-antagonist
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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: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: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:qHTS Validation Assay for Inhibitors of Ubiquitin-specific Protease USP2a Using CHOP2...
来源:NCGC
靶标:ubiquitin carboxyl-terminal hydrolase 2 isoform a [Homo sapiens]
External Id:UBCH001
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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: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:Rescue cell viability in cybrid cells with a genetic mutation in complex 1 of the mit...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:N/A
External Id:HMS1315
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| 5-Methyl-6[[3-[4-(2-methoxyphenyl)-1-piperazinyl]propyl]amino]-1,3-dimethyluracil |