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乙酰水杨酸, 环氧化酶抑制剂

COX-1 Selective Inhibitors
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库存信息

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货号 (SKU) 包装规格 是否现货 价格 数量
A407995-1ml
1ml 现货 Stock Image
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Compound libraries (12333)

基本描述

英文别名 Acetylsalicylic acid, ASA | 2-​(acetyloxy)​-benzoic acid
规格或纯度 Moligand™, 10mM in DMSO
英文名称 Aspirin (NSC 27223)
生化机理 阿司匹林(NSC 27223,乙酰水杨酸,ASA)是一种水杨酸盐,也是不可逆的 COX1 和 COX2 抑制剂,可用作镇痛剂来缓解轻微疼痛,用作解热剂来退烧,还可用作消炎药。阿司匹林可诱导自噬和刺激有丝分裂。
储存温度 -80℃储存
运输条件 超低温冰袋运输
作用类型 抑制剂
作用机制 环氧化酶抑制剂
产品介绍

无气味。微带酸味。在干燥空气中稳定,在潮湿空气中逐渐水解成水杨酸和乙酸。遇沸水或溶于氢氧化钠碱溶液和碳酸碱溶液中全部分解。溶于乙醇、乙醚和氯仿。检定锰。有机合成。 乙酰水杨酸靠抑制环化加氧酶(cyclooxygenase,前列腺素H合成酶)阻止前列腺索的生产,特别是针对COX-1同种型有很高的选择性。其抗血栓效果就是由于抑制了血小板中起凝血和血小板凝聚作用的COX-1。

Information

Aspirin (NSC 27223, Acetylsalicylic acid, ASA) is a salicylate, and irreversibleCOX1andCOX2inhibitor, used as an analgesic to relieve minor aches and pains, as an antipyretic to reduce fever, and as an anti-inflammatory medication. Aspirin inducesautophag
In vitro

Aspirin inhibits the activation of NF-kappa B, thus prevents the degradation of the NF-kappa B inhibitor, I kappa B, and therefore NF-kappa B is retained in the cytosol. Aspirin also inhibits NF-kappa B-dependent transcription from the Ig kappa enhancer and the human immunodeficiency virus (HIV) long terminal repeat (LTR) in transfected T cells. Aspirin and salicylate are mediated in part by their specific inhibition of IKK-beta, thereby preventing activation by NF-kappaB of genes involved in the pathogenesis of the inflammatory response. Aspirin is protective against neurotoxicity elicited by the excitatory amino acid glutamate in rat primary neuronal cultures and hippocampal slices. Aspirin triggers transcellular biosynthesis of a previously unrecognized class of eicosanoidsduring coincubations of human umbilical vein endothelial cells (HUVEC) and neutrophils [polymorphonuclear leukocytes (PMN)]. Aspirin evokes a unique class of eicosanoids formed by acetylated PGHS-2 and 5-lipoxygenase interactions. Aspirin treatment inhibits the phosphorylation of IRS-1 at Ser307 as well as the phosphorylation of JNK, c-Jun, and degradation of IkappaBalpha in 3T3-L1 and Hep G2 cells treated with tumor necrosis factor (TNF)-alpha. Aspirin treatment inhibits phosphorylation of Akt and the mammalian target of rapamycin (but not extracellular regulated kinase or PKCzeta) in response to TNF-alpha. Aspirin rescues insulin-induced glucose uptake in 3T3-L1 adipocytes pretreated with TNF-alpha.

In vivo


Cell Data

cell lines:

Concentrations:

Incubation Time:

Powder Purity:≥99%

产品属性

ALogP 1.2

关联靶点(人)

NAPRT Tchem 烟酸磷酸核糖基转移酶(Nicotinate phosphoribosyltransferase) (0 活性数据)
活性类型 活性值-log(M) 作用机制 期刊 参考文献(PubMed IDs)
PTGS1 Tclin 前列腺素 G/H 合酶 1(Prostaglandin G/H synthase 1) (1 活性数据)
活性类型 活性值-log(M) 作用机制 期刊 参考文献(PubMed IDs)
PTGS2 Tclin 前列腺素 G/H 合酶 2(Prostaglandin G/H synthase 2) (1 活性数据)
活性类型 活性值-log(M) 作用机制 期刊 参考文献(PubMed IDs)
ASIC3 Tchem 酸敏感离子通道 3(Acid-sensing ion channel 3) (1 活性数据)
活性类型 活性值-log(M) 作用机制 期刊 参考文献(PubMed IDs)

名称和识别符

EC号 200-064-1
Isomeric SMILES CC(=O)OC1=CC=CC=C1C(=O)O
UN Number 2811
Packing Group I
分子量 180.16
Beilstein号 779271
Reaxy-Rn 779271
Reaxys-RN link address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=779271&ln=

化学和物理性质

溶解性 Solubility (25°C) In vitro Ethanol: 7 mg/mL (33.45 mM); DMSO: 2 mg/mL (9.55 mM); Water: Insoluble;
闪点(℉) 446 °F
闪点(℃) 250℃
熔点 136-140°C

安全和危险性(GHS)

WGK Germany 1
RTECS VO0700000
Class 6.1
Merck Index 851
个人防护装备 dust mask type N95 (US),Eyeshields,Faceshields,Gloves

质检证书(CoA,COO,BSE/TSE 和分析图谱)

C of A & Other Certificates(BSE/TSE, COO):
输入批号以搜索分析图谱:

溶液计算器