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卡非多

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卡非多结构式
卡非多结构式
品牌特惠专场
常用名 卡非多 英文名 Carphedon
CAS号 77472-70-9 分子量 218.252
密度 1.2±0.1 g/cm3 沸点 486.4±45.0 °C at 760 mmHg
分子式 C12H14N2O2 熔点 N/A
MSDS N/A 闪点 247.9±28.7 °C

 卡非多用途


Phenylpiracetam(Phenotropyl; Phenotropil)是piracetam的苯基衍生物,活性较piracetam高30到60倍。

 卡非多名称

中文名 4-苯基-2-吡咯烷酮-1-乙酰胺
英文名 2-(2-Oxo-4-phenylpyrrolidin-1-yl)acetamide
中文别名 苯基吡拉西坦 | 芳妥西坦 | 4-苯基吡拉西坦 | 卡非多
英文别名 更多

 卡非多生物活性

描述 Phenylpiracetam(Phenotropyl; Phenotropil)是piracetam的苯基衍生物,活性较piracetam高30到60倍。
相关类别
参考文献

[1]. Zvejniece L, et al. Investigation into stereoselective pharmacological activity of phenotropil. Basic Clin Pharmacol Toxicol. 2011 Nov;109(5):407-12.

 卡非多物理化学性质

密度 1.2±0.1 g/cm3
沸点 486.4±45.0 °C at 760 mmHg
分子式 C12H14N2O2
分子量 218.252
闪点 247.9±28.7 °C
精确质量 218.105530
PSA 64.39000
LogP 0.16
InChIKey LYONXVJRBWWGQO-UHFFFAOYSA-N
SMILES NC(=O)CN1CC(c2ccccc2)CC1=O
蒸汽压 0.0±1.2 mmHg at 25°C
折射率 1.580

 卡非多毒性和生态

 卡非多安全信息

海关编码 2933990090

 卡非多合成线路

~99%

卡非多结构式

卡非多

77472-70-9

文献:Pharmaceutical Chemistry Journal, , vol. 14, # 11 p. 776 - 780 Khimiko-Farmatsevticheskii Zhurnal, , vol. 14, # 11 p. 43 - 48

~81%

卡非多结构式

卡非多

77472-70-9

文献:J. Gen. Chem. USSR (Engl. Transl.), , vol. 58, # 5 p. 1093 - 1102,970 - 979

~%

卡非多结构式

卡非多

77472-70-9

文献:J. Gen. Chem. USSR (Engl. Transl.), , vol. 58, # 5 p. 1093 - 1102,970 - 979

~%

卡非多结构式

卡非多

77472-70-9

文献:J. Gen. Chem. USSR (Engl. Transl.), , vol. 58, # 5 p. 1093 - 1102,970 - 979

~%

卡非多结构式

卡非多

77472-70-9

文献:J. Gen. Chem. USSR (Engl. Transl.), , vol. 58, # 5 p. 1093 - 1102,970 - 979

~%

卡非多结构式

卡非多

77472-70-9

文献:Pharmaceutical Chemistry Journal, , vol. 14, # 11 p. 776 - 780 Khimiko-Farmatsevticheskii Zhurnal, , vol. 14, # 11 p. 43 - 48

~%

卡非多结构式

卡非多

77472-70-9

文献:Pharmaceutical Chemistry Journal, , vol. 14, # 11 p. 776 - 780 Khimiko-Farmatsevticheskii Zhurnal, , vol. 14, # 11 p. 43 - 48

 卡非多海关

海关编码 2933990090
中文概述 2933990090. 其他仅含氮杂原子的杂环化合物. 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, 乌洛托品请注明外观, 6-己内酰胺请注明外观, 签约日期
Summary 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 卡非多靶点实验

查看更多实验

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
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: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
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: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
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.
实验名称:Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
来源:Broad Institute
靶标:FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id:2147-01_Inhibitor_SinglePoint_HTS_Activity
实验名称:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
来源:Broad Institute
靶标:N/A
External Id:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity
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
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 卡非多英文别名

fonturacetam
UNII:99QW5JU66Y
Carphedon
Phenylpiracetam
4-Phenyl-2-pyrrolidone-1-acetamide
2-(2-Oxo-4-phenyl-1-pyrrolidinyl)acetamide
2-(2-oxo-4-phenylpyrrolidin-1-yl)acetamide
4-Phenylpiracetam
Phenotropil
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