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3-[(2-乙酰氧基)乙基氨基羰基]吡啶

更新时间:2025-09-12 23:40:39

3-[(2-乙酰氧基)乙基氨基羰基]吡啶结构式
3-[(2-乙酰氧基)乙基氨基羰基]吡啶结构式
品牌特惠专场
常用名 3-[(2-乙酰氧基)乙基氨基羰基]吡啶 英文名 SG 209
CAS号 83440-03-3 分子量 208.21400
密度 1.182g/cm3 沸点 430.7ºC at 760 mmHg
分子式 C10H12N2O3 熔点 N/A
MSDS 美版 闪点 214.3ºC

 3-[(2-乙酰氧基)乙基氨基羰基]吡啶用途


SG-209 is a potassium channel opener.

 3-[(2-乙酰氧基)乙基氨基羰基]吡啶名称

中文名 3-[(2-乙酰氧基)乙基氨基羰基]吡啶
英文名 SG 209,N-[2-(Acetoxy)ethyl]-3-pyridinecarboxamide
英文别名 更多

 3-[(2-乙酰氧基)乙基氨基羰基]吡啶物理化学性质

密度 1.182g/cm3
沸点 430.7ºC at 760 mmHg
分子式 C10H12N2O3
分子量 208.21400
闪点 214.3ºC
精确质量 208.08500
PSA 68.29000
LogP 0.76540
InChIKey JQICNNKLTFYSLS-UHFFFAOYSA-N
SMILES CC(=O)OCCNC(=O)c1cccnc1
外观性状 固体
折射率 1.521
储存条件 -20°C, 密封, 干燥

 3-[(2-乙酰氧基)乙基氨基羰基]吡啶安全信息

个人防护装备 Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
安全声明 (欧洲) 22-24/25
危险品运输编码 NONH for all modes of transport
海关编码 2933399090

 3-[(2-乙酰氧基)乙基氨基羰基]吡啶合成线路

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3-[(2-乙酰氧基)乙基氨基羰基]吡啶结构式

3-[(2-乙酰氧基)乙基氨基羰基]吡啶

83440-03-3

文献:TERNANSKY, Robert Patent: WO2007/38772 A1, 2007 ; Location in patent: Example 2 ; WO 2007/038772 A1

 3-[(2-乙酰氧基)乙基氨基羰基]吡啶上下游产品

3-[(2-乙酰氧基)乙基氨基羰基]吡啶上游产品  2

3-[(2-乙酰氧基)乙基氨基羰基]吡啶下游产品  0

 3-[(2-乙酰氧基)乙基氨基羰基]吡啶海关

海关编码 2933399090
中文概述 2933399090. 其他结构含非稠合吡啶环的化合物. 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 2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 3-[(2-乙酰氧基)乙基氨基羰基]吡啶文献9

更多文献
ATP-sensitive potassium channel activation induces angiogenesis in vitro and in vivo.

J. Pharmacol. Exp. Ther. 354 , 79-87, (2015)

Intense research is conducted to identify new molecular mechanisms of angiogenesis. Previous studies have shown that the angiogenic effects of hydrogen sulfide (H2S) depend on the activation of ATP-se...

Nicorandil inhibits degranulation and TNF-alpha release from RBL-2H3 cells.

Inflamm. Res. 51 , 176-181, (2002)

Nicorandil is a potassium channel opener and nitric oxide (NO) donor, and the hypothesis was tested that these modes of action may inhibit cellular degranulation and release of tumour necrosis factor-...

A further study of the vasodilator and negative inotropic mechanisms of action of nicorandil and its congeners in the canine heart.

Cardiovasc. Drugs Ther. 8 , 227-234, (1994)

The vasodilator and negative inotropic mechanisms of action of nicorandil and its congeners (SG-209, SG-103, and SG-86) were investigated in isolated canine papillary muscle preparations cross-circula...

 3-[(2-乙酰氧基)乙基氨基羰基]吡啶靶点实验

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:Primary qHTS for small molecule stabilizers of the endoplasmic reticulum resident pro...
来源:NCGC
靶标:N/A
External Id:SERCaMPGLuc-p1-antagonist
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: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
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:Tocris HTS for Inhibitors of Aerobactin Synthetase lucA
来源:23265
External Id:IucA Pilot Assay Tocris Library
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 3-[(2-乙酰氧基)乙基氨基羰基]吡啶英文别名

sg 209
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