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依托考昔

规格或纯度: ≥98.0%
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货号 (SKU) 包装规格 是否现货 价格 数量
E126660-10mg
10mg 现货 Stock Image
E126660-50mg
50mg 现货 Stock Image
E126660-250mg
250mg 现货 Stock Image
E126660-1g
1g 现货 Stock Image
E126660-5g
5g 现货 Stock Image
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COX-2 Inhibitor

基本描述

规格或纯度 ≥98.0%
英文名称 Etoricoxib
别名 MK-663|MK-0663|依托考昔|5-氯-6'-甲基-3-[4-(甲磺酰基)苯基]]-2,3'-联吡啶|5-氯-3-[4-(甲磺酰基)苯基]-2-(2-甲基-5-吡啶基)吡啶
英文别名 Etoricoxib|202409-33-4|Arcoxia|Tauxib|Nucoxia|Algix|MK-0663|5-Chloro-6'-methyl-3-(4-(methylsulfonyl)phenyl)-2,3'-bipyridine|MK-663|L-791456|MK 0663|2,3'-Bipyridine, 5-chloro-6'-methyl-3-[4-(methylsulfonyl)phenyl]-|5-chloro-6'-methyl-3-[4-(methylsulfonyl)p
生化机理 Etoricoxib is a specific inhibitor of COX-2(Cyclooxygenase-2)
储存温度 2-8°C储存,充氩
运输条件 冰袋运输
备注 10mg售完停产,不再备货
产品介绍

Etoricoxib(MK-0663)能选择性抑制COX-2,IC50为1.1_mu_M(LPS诱导的前列腺素E2合成实验),而对COX-1的IC50则为116_mu_M(凝血后血清血栓素B2生成实验)。A specific inhibitor of COX-2.

EtoricoxibEtoricoxib(MK-0663) selectively inhibited COX-2 in human whole blood assays in vitro, with an IC50 value of1.1 ± 0.1 μM for COX-2 (LPS-induced prostaglandin E2 synthesis), compared with an IC50 value of 116 ± 8 μM for COX-1 (serum thromboxane B2 generation after clotting of the blood).
A specific inhibitor of COX-2.

名称和标识符

IUPAC Name 5-chloro-2-(6-methylpyridin-3-yl)-3-(4-methylsulfonylphenyl)pyridine
INCHI InChI=1S/C18H15ClN2O2S/c1-12-3-4-14(10-20-12)18-17(9-15(19)11-21-18)13-5-7-16(8-6-13)24(2,22)23/h3-11H,1-2H3
InChi Key MNJVRJDLRVPLFE-UHFFFAOYSA-N
Canonical SMILES CC1=NC=C(C=C1)C2=C(C=C(C=N2)Cl)C3=CC=C(C=C3)S(=O)(=O)C
分子式

C18H15ClN2O2S

PubChem CID 123619
Beilstein号 8073797
分子量 358.84

化学和物理性质

溶解性 Soluble in DMSO, and methanol

安全信息

象形图
ghs06

Toxic

信号词 Danger
危险声明 H302: Harmful if swallowed
H310: Fatal in contact with skin
预防措施声明 P280,P310,P302+P350
WGK Germany 3

靶标

Target ID 1376
名称 COX-2
缩写名 SHP2
家族 Cyclooxygenase
别名 DKFZp762B2210
基因和蛋白信息
Species Transmembrane Domains Amino Acids Chromosomal Location Gene Symbol Gene Name
Human 2 604 1q31.1 PTGS2 prostaglandin-endoperoxide synthase 2
Mouse 2 604 1 63.84 cM Ptgs2 prostaglandin-endoperoxide synthase 2
Rat 2 604 13q21 Ptgs2 prostaglandin-endoperoxide synthase 2
Ensembl Gene ENSG00000073756 (Hs) , ENSMUSG00000032487 (Mm) , ENSRNOG00000002525 (Rn)
Entrez Gene 19225 (Mm) , 29527 (Rn) , 5743 (Hs)
OMIM 600262 (Hs)
Protein GI 148747270 (Rn) , 4506265 (Hs) , 31981525 (Mm)
UniProtKB P35354 (Hs) , Q05769 (Mm) , P35355 (Rn)
DrugBank Target P35354 (Hs)
CATH/Gene3D 1.10.640.10 (N/A)
ChEMBL Target CHEMBL2977 (Rn) , CHEMBL230 (Hs) , CHEMBL4321 (Mm)

关联配体

Ligand ID 2896
名称 etoricoxib
别名 MK 0663
类别 Synthetic organic
学名 5-chloro-2-(6-methylpyridin-3-yl)-3-(4-methylsulfonylphenyl)pyridine
生物活性评价 The sulfonamide class of antibacterial compounds are primarily bacteriostatic agents and have a broad spectrum of activity against both Gram-positive and Gram-negative species of bacteria (reviewed in ).
评价 Etoricoxib is a selective COX-2 inhibitor, non-steroidal anti-inflammatory (NSAID) drug.

COVID-19: Etoricoxib offers potential to be repositioned to inhibit cytokine storm in COVID-19 patients .
配体家族 Non-steroidal anti-inflammatory ligands

参考文献

1. Wang R.  (2021)  Etoricoxib may inhibit cytokine storm to treat COVID-19..  Med Hypotheses,  150  (13):  (110557).  [PMID:33730601]

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