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黄嘌呤胺同类物

更新时间:2025-11-24 22:24:09

黄嘌呤胺同类物结构式
黄嘌呤胺同类物结构式
品牌特惠专场
常用名 黄嘌呤胺同类物 英文名 Xanthine amine congener
CAS号 96865-92-8 分子量 428.48
密度 1.262g/cm3 沸点 N/A
分子式 C21H28N6O4 熔点 N/A
MSDS 中文版 美版 闪点 N/A

 黄嘌呤胺同类物用途


黄嘌呤胺同系物是一种非选择性腺苷受体拮抗剂[1]。黄嘌呤胺同系物诱导小鼠惊厥[2]。

 黄嘌呤胺同类物名称

中文名 黄嘌呤胺同类物
英文名 N-(2-aminoethyl)-2-[4-(2,6-dioxo-1,3-dipropyl-7H-purin-8-yl)phenoxy]acetamide
英文别名 更多

 黄嘌呤胺同类物物理化学性质

密度 1.262g/cm3
分子式 C21H28N6O4
分子量 428.48
精确质量 428.21700
PSA 137.03000
LogP 1.91820
InChIKey FIQGIOAELHTLHM-UHFFFAOYSA-N
SMILES CCCn1c(=O)c2[nH]c(-c3ccc(OCC(=O)NCCN)cc3)nc2n(CCC)c1=O
折射率 1.586
储存条件 -20°C,密闭,干燥

 黄嘌呤胺同类物安全信息

个人防护装备 Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
危险品运输编码 NONH for all modes of transport
WGK德国 3

 黄嘌呤胺同类物文献30

更多文献
Chaperoning of the A1-adenosine receptor by endogenous adenosine - an extension of the retaliatory metabolite concept.

Mol. Pharmacol. 87(1) , 39-51, (2015)

Cell-permeable orthosteric ligands can assist folding of G protein-coupled receptors in the endoplasmic reticulum (ER); this pharmacochaperoning translates into increased cell surface levels of recept...

Allosteric interactions across native adenosine-A3 receptor homodimers: quantification using single-cell ligand-binding kinetics.

FASEB J. 25(10) , 3465-76, (2011)

A growing awareness indicates that many G-protein-coupled receptors (GPCRs) exist as homodimers, but the extent of the cooperativity across the dimer interface has been largely unexplored. Here, measu...

Hyperactivation of D1 and A2A receptors contributes to cognitive dysfunction in Huntington's disease.

Neurobiol. Dis. 74 , 41-57, (2015)

Stimulation of dopamine D1 receptor (D1R) and adenosine A2A receptor (A2AR) increases cAMP-dependent protein kinase (PKA) activity in the brain. In Huntington's disease, by essentially unknown mechani...

 黄嘌呤胺同类物靶点实验

查看更多实验

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:Selectivity, ratio of affinity towards adenosine A3 to A2A
来源:ChEMBL
靶标:N/A
External Id:CHEMBL838353
实验名称:Selectivity, ratio of affinity towards adenosine A3 to A1
来源:ChEMBL
靶标:N/A
External Id:CHEMBL838352
实验名称:Inhibition of neurosphere proliferation of mouse neural precursor cells by MTT assay
来源:ChEMBL
靶标:N/A
External Id:CHEMBL1266185
实验名称:Selectivity, ratio of affinity towards adenosine A2A to A1
来源:ChEMBL
靶标:N/A
External Id:CHEMBL838351
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: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
实验名称:Ratio against A1 adenosine receptor to the A2 adenosine receptor (guinea pig forebrai...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL849651
实验名称:Ratio of Ki at A2 receptor to that of A1 receptor
来源:ChEMBL
靶标:Adenosine receptors; A1 & A2
External Id:CHEMBL849650
实验名称:Human A3 receptor (Adenosine receptors)
来源:IUPHAR-DB
靶标:A3 receptor (Adenosine receptors) [Homo sapiens]
External Id:21_Human
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 黄嘌呤胺同类物英文别名

Papaxac
XAC
Lopac-X-103
xanthine amine congener
Xanthine amine congener xac
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