福莫卡因

• 常用名: 福莫卡因
• 英文名: Fomocaine
• CAS号: 17692-39-6
• 分子量: 311.42
• 密度: 1.081g/cm3
• 沸点: 469ºC at 760 mmHg
• 分子式: C₂₀H₂₅NO₂
• 熔点: N/A
• 闪点: 153.5ºC

福莫卡因用途

福莫卡因(P 652)是一种口服活性局部麻醉剂。福莫卡因具有抗心律失常活性[1][2]。

福莫卡因名称

• 中文名: 福莫卡因
• 英文名: 4-[3-[4-(phenoxymethyl)phenyl]propyl]morpholine

福莫卡因生物活性

• 描述: 福莫卡因(P 652)是一种口服活性局部麻醉剂。福莫卡因具有抗心律失常活性[1][2]。
• 相关类别:
  研究领域 >> 心血管疾病
  信号通路 >> 其他 >> 其他
  研究领域 >> 神经疾病
• 参考文献:

  [1]. Lupp A, et al. In vitro interactions with the Cytochrome P450 system, toxicity, and local anaesthetic effects of Fomocaine Alkylmorpholine derivatives in rats. Arzneimittelforschung. 2006;56(1):1-11.

  [2]. Bräunig B, et al. Antiarrhythmic activity of the local anaesthetic fomocaine and some of its analogues. Arzneimittelforschung. 1989 Nov;39(11):1436-9.

福莫卡因物理化学性质

• 密度: 1.081g/cm3
• 沸点: 469ºC at 760 mmHg
• 分子式: C₂₀H₂₅NO₂
• 分子量: 311.42
• 闪点: 153.5ºC
• 精确质量: 311.18900
• PSA: 21.70000
• LogP: 3.46830
• InChIKey: CVHGCWVMTZWGAY-UHFFFAOYSA-N
• SMILES: c1ccc(OCc2ccc(CCCN3CCOCC3)cc2)cc1
• 蒸汽压: 5.7E-09mmHg at 25°C
• 折射率: 1.56

福莫卡因安全信息

• 海关编码: 2934999090

福莫卡因海关

• 海关编码: 2934999090
• 中文概述: 2934999090. 其他杂环化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0%
• 申报要素: 品名, 成分含量, 用途
• Summary: 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

福莫卡因靶点实验

查看更多实验

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：Primary qHTS assay for inhibitors of alpha-synuclein gene (SNCA) expression 来源：NCGC External Id：SNCA-p-activity-luciferase

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：Cytochrome P450 Family 1 Subfamily A Member 2 (CYP1A2) small molecule antagonists: lu... 来源：824 External Id：CYP273

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：qHTS of TDP-43 Inhibitors: NCGC Sytravon Library Screen 来源：NCGC External Id：tdp43-p2-repeat

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

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

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

实验名称：p53 small molecule agonists, cell-based qHTS assay with rat liver microsomes: qHTS ce... 来源：824 靶标：N/A External Id：P53MS958

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福莫卡因英文别名

• 4-{3-[4-(phenoxymethyl)phenyl]propyl}morpholine
• Fomocaine
• Fomocain
• 4-[3-(4-Phenoxymethyl-phenyl)-propyl]-morpholin