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N-(2-(1H-咪唑-5-基)乙基)-3-氨基丙酰胺

更新时间:2025-08-25 16:04:42

N-(2-(1H-咪唑-5-基)乙基)-3-氨基丙酰胺结构式
N-(2-(1H-咪唑-5-基)乙基)-3-氨基丙酰胺结构式
品牌特惠专场
常用名 N-(2-(1H-咪唑-5-基)乙基)-3-氨基丙酰胺 英文名 Carcinine hydrochloride salt
CAS号 56897-53-1 分子量 182.22
密度 1.2±0.1 g/cm3 沸点 547.6±40.0 °C at 760 mmHg
分子式 C8H14N4O 熔点 N/A
MSDS N/A 闪点 285.0±27.3 °C

 N-(2-(1H-咪唑-5-基)乙基)-3-氨基丙酰胺用途


Alistin(Carcinine;β-丙氨酸组胺)是一种选择性组胺H3拮抗剂,对氧化应激小鼠的视网膜具有抗氧化活性和神经保护作用[1][2]。

 N-(2-(1H-咪唑-5-基)乙基)-3-氨基丙酰胺名称

中文名 N-2-[(4-1H-咪唑基)乙基]-3-氨基丙酰胺二盐酸盐
英文名 Carcinine Hydrochloride
英文别名 更多

 N-(2-(1H-咪唑-5-基)乙基)-3-氨基丙酰胺生物活性

描述 Alistin(Carcinine;β-丙氨酸组胺)是一种选择性组胺H3拮抗剂,对氧化应激小鼠的视网膜具有抗氧化活性和神经保护作用[1][2]。
相关类别
参考文献

[1]. Zhong Chen, et al. Pharmacological effects of carcinine on histaminergic neurons in the brain. Br J Pharmacol. 2004 Nov;143(5):573-80.   

[2]. Lea D Marchette, et al. Carcinine has 4-hydroxynonenal scavenging property and neuroprotective effect in mouse retina. Invest Ophthalmol Vis Sci. 2012 Jun 20;53(7):3572-83.  

 N-(2-(1H-咪唑-5-基)乙基)-3-氨基丙酰胺物理化学性质

密度 1.2±0.1 g/cm3
沸点 547.6±40.0 °C at 760 mmHg
分子式 C8H14N4O
分子量 182.22
闪点 285.0±27.3 °C
精确质量 182.116760
PSA 87.29000
LogP -1.83
InChIKey ANRUJJLGVODXIK-UHFFFAOYSA-N
SMILES NCCC(=O)NCCc1cnc[nH]1
蒸汽压 0.0±1.5 mmHg at 25°C
折射率 1.559
储存条件 20°C

 N-(2-(1H-咪唑-5-基)乙基)-3-氨基丙酰胺安全信息

危害码 (欧洲) Xi
风险声明 (欧洲) 36/37/38
安全声明 (欧洲) 26-36
海关编码 2933290090

 N-(2-(1H-咪唑-5-基)乙基)-3-氨基丙酰胺上下游产品

N-(2-(1H-咪唑-5-基)乙基)-3-氨基丙酰胺上游产品  3

N-(2-(1H-咪唑-5-基)乙基)-3-氨基丙酰胺下游产品  0

 N-(2-(1H-咪唑-5-基)乙基)-3-氨基丙酰胺海关

海关编码 2933290090
中文概述 2933290090. 其他结构含非稠合咪唑环的化合物. 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 2933290090. other compounds containing an unfused imidazole ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 N-(2-(1H-咪唑-5-基)乙基)-3-氨基丙酰胺靶点实验

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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
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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: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...
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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...
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External Id:SIAE_INH_FP_1536_1X%INH PRUN
实验名称:Absorbance-based primary biochemical high throughput screening assay to identify acti...
来源:The Scripps Research Institute Molecular Screening Center
靶标:caspase-3 preproprotein [Homo sapiens]
External Id:PROCASPASE3_ACT_EPIABS_1536_1X%ACT PRUN
实验名称:uHTS identification of small molecule modulators of NR3A
来源:Burnham Center for Chemical Genomics
靶标:N/A
External Id:SBCCG-A1015-NR3A-Primary-Assay
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 N-(2-(1H-咪唑-5-基)乙基)-3-氨基丙酰胺英文别名

carcinine
N-[2-(1H-Imidazol-5-yl)ethyl]-β-alaninamide
3-amino-N-[2-(1H-imidazol-5-yl)ethyl]propanamide
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