ウミフェノビル

ウミフェノビル 化学構造式
131707-25-0
CAS番号.
131707-25-0
化学名:
ウミフェノビル
别名:
6-ブロモ-4-ジメチルアミノメチル-5-ヒドロキシ-1-メチル-2-フェニルチオメチル-1H-インドール-3-カルボン酸エチル·塩酸塩;アルビドール;ウミフェノビル;メチル6-ブロモ-4-[(ジメチルアミノ)メチル]-5-ヒドロキシ-1-メチル-2-[(フェニルスルファニル)メチル]インドール-3-カルボキシラート;メチル6-ブロモ-4-[(ジメチルアミノ)メチル]-5-ヒドロキシ-1-メチル-2-[(フェニルスルファニル)メチル]-1H-インドール-3-カルボキシラート;6-ブロモ-4-(ジメチルアミノメチル)-5-ヒドロキシ-1-メチル-2-[(フェニルチオ)メチル]-1H-インドール-3-カルボン酸メチル;エチル 6-ブロモ-4-[(ジメチルアミノ)メチル]-5-ヒドロキシ-1-メチル-2-[(フェニルスルファニル)メチル]-1H-インドール-3-カルボキシラート
英語名:
Arbidol
英語别名:
UMifenovir;ethyl 6-bromo-4-[(dimethylamino)methyl]-5-hydroxy-1-methyl-2-(phenylsulfanylmethyl)indole-3-carboxylate;Ethyl 6-bromo-5-hydroxy-1-methyl-4-((dimethylamino)methyl)-2-[(phenylthio)methyl]-1H-indole-3-carboxylate;Arbidol;2H6]-Umifenovir;Arbidol USP/EP/BP;Abbidore intermediate 6;Arbidol Pills Umifenovir;Arbidol CAS NO.131707-25-0;INTERMEDIATE:ARBIDOLHYDROCHLORIDE
CBNumber:
CB6946906
化学式:
C22H25BrN2O3S
分子量:
477.41
MOL File:
131707-25-0.mol

ウミフェノビル 物理性質

沸点 :
591.8±50.0 °C(Predicted)
比重(密度) :
1.37±0.1 g/cm3(Predicted)
貯蔵温度 :
-20°C Freezer, Under inert atmosphere
溶解性:
クロロホルム(微量)、メタノール(微量、加温)
外見 :
個体
酸解離定数(Pka):
6.02±0.50(Predicted)
色:
ペールブラウンからライトブラウン

安全性情報

ウミフェノビル 価格 もっと(3)

メーカー 製品番号 製品説明 CAS番号 包装 価格 更新時間 購入
富士フイルム和光純薬株式会社(wako) W01MAS099485 アルビドール
Arbidol
131707-25-0 250mg ¥150400 2024-03-01 購入
富士フイルム和光純薬株式会社(wako) W01MAS099485 アルビドール
Arbidol
131707-25-0 500mg ¥231800 2024-03-01 購入
富士フイルム和光純薬株式会社(wako) W01MAS099485 アルビドール
Arbidol
131707-25-0 1g ¥356500 2024-03-01 購入

ウミフェノビル 化学特性,用途語,生産方法

効能

抗ウイルス薬

説明

Arbidol, or umifenovir, an indole-derivative with broad-spectrum activity against both enveloped and non-enveloped viruses,was initially approved in China and Russia for the treatment of influenza A and B.Arbidol is believed to block the entry of influenza virus (A and B) into the host cells by increasing the stability of the hemagglutinin (HA) and hampering low pH reorganizations necessary for fusion machinery of hemagglutinin with the membrane.Arbidol could interfere with advanced stages of the viral life cycle, in that it is capable of interacting with both viral proteins and lipids.Regarding its structure, the presence of amine in position 4 and the hydroxyl moiety in position 5 is crucial for its antiviral activity. It is reported that 40% of the drug could be excreted unchanged after the administration while its half-life is between 17 and 21h.

使用

Umifenovir is an intermediate in synthesizing Arbidol Sulfoxide (A766005), a metabolite of Arbidol (A766000) which is a medicinal agent for treating viral infections.

生物活性

Arbidol Arbidol is a broad spectrum antiviral. Displays activity against a range of respiratory and hepatitis viruses including influenza A, B and C, adenovirus, and hepatitis B and C. Increases stability of influenza viral hemagglutinins (HA) and prevents low-pH HA transition so inhibiting viral fusion. Also inhibits SARS-CoV-2 infection in vitro (IC50 = 4.11 μM).

作用機序

Probable Mechanism of Action
lt is hypothesized that arbidol inhibits the contact between the virus and host cell that further prevents the entry of the virus into host cells. It is also being predicted that arbidol also interferes with the late stages of virus cycle by interacting with lipids and proteins of the virus which are essential for the viral replication;probably arbidol binds with these essential components that further inhibit viral replication (Boriskin et al., 2008).
Umifenovir inhibits membrane fusion.Umifenovir prevents contact between the virus and target host cells. Fusion between the viral envelope (surrounding the viral capsid) and the cell membrane of the target cell is inhibited. This prevents viral entry to the target cell, and therefore protects it from infection.
Some evidence suggests that the drug’s actions are more effective at preventing infections from RNA viruses than infections from DNA viruses.
As well as specific antiviral action against both influenza A and influenza B viruses, umifenovir exhibits modulatory effects on the immune system. The drug stimulates a humoral immune response, induces interferon-production, and stimulates the phagocytic function of macrophages.
https://newdrugapprovals.org

臨床応用

Arbidol in Treatment of covID-19
Although,arbidol is not approved by US-FDA for the treatment of cOVID-19,some pre-clinical and clinical studies have reported that it may be a very efficacious therapeutic molecule for COVID-19 (Deng et al.,2020; Wang et al.,2020).Arbidol has been included in the latest version of the guidelines issued by the National Health Commission (NHC) of the people's republic of China for the prevention, diagnosis, and treatment of novel coronavirus induced pneumonia at the recommended dose of 200 mg, 3 times/day for 10 days for adults (National Health Commission,China).
An in-vitro study claimed that arbidol is effective against COVID-19 at the concentration range of 10-30 uM (News: Abidol and darunavir can effectively inhibit corona virus (2020). A retrospective study conducted by Deng and colleagues reported that patients who received oral arbidol plus lopinavir/ritonavir showed improvement in clinical symptoms and reduced viral load as a compared to the patients who received lopinavir/ritonavir alone (Deng et al.,2020).A randomized multi-centre controlled clinical trial of arbidol in the patients with cOVID-19 is currently running in China (ChiCTR2000029573).
Besides this, one more study was conducted on 69 patients of COVID-19.In this study, it was reported that the administration of arbidol at the dose of 0.4 g,TID for 9 days improves the discharging rate from the hospital and also decreases the mortality rate of patients (Wang et al.,2020). In addition,another study also reported that arbidol is more superior to the combination therapy of lopinavir/ritonavir (Zhu et al.,2020).
Arbidol: a broad-spectrum antiviral compound that blocks viral fusion
Arbidol: A potential antiviral drug for the treatment of SARS-CoV-2 by blocking trimerization of the spike glycoprotein

ウミフェノビル 上流と下流の製品情報

原材料

準備製品


ウミフェノビル 生産企業

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131707-25-0(ウミフェノビル)キーワード:


  • 131707-25-0
  • Arbidol
  • INTERMEDIATE:ARBIDOLHYDROCHLORIDE
  • 1H-Indole-3-carboxylic acid, 6-bromo-4-((dimethylamino)methyl)-5-hydroxy-1-methyl-2-((phenylthio)methyl)-, ethyl ester
  • ETHYL6-BROMO-4-((DIMETHYLAMINO)METHYL)-5-HYDROXY-1-METHYL.
  • ethyl 6-bromo-4-((dimethylamino)methyl)-5-hydroxy-1-methyl-2-((phenylthio)methyl)-1H-indole-3-carboxylate
  • Arbidol Pills Umifenovir
  • Arbidol USP/EP/BP
  • 6-bromo-4-[(dimethylazaniumyl)methyl]-3-ethoxycarbonyl-1-methyl-2-(phenylsulfanylmethyl)indol-5-olate
  • Ethyl 6-bromo-5-hydroxy-1-methyl-4-((dimethylamino)methyl)-2-[(phenylthio)methyl]-1H-indole-3-carboxylate
  • UMifenovir
  • ethyl 6-bromo-4-[(dimethylamino)methyl]-5-hydroxy-1-methyl-2-(phenylsulfanylmethyl)indole-3-carboxylate
  • Arbidol CAS NO.131707-25-0
  • 2H6]-Umifenovir
  • Abbidore intermediate 6
  • 6-ブロモ-4-ジメチルアミノメチル-5-ヒドロキシ-1-メチル-2-フェニルチオメチル-1H-インドール-3-カルボン酸エチル·塩酸塩
  • アルビドール
  • ウミフェノビル
  • メチル6-ブロモ-4-[(ジメチルアミノ)メチル]-5-ヒドロキシ-1-メチル-2-[(フェニルスルファニル)メチル]インドール-3-カルボキシラート
  • メチル6-ブロモ-4-[(ジメチルアミノ)メチル]-5-ヒドロキシ-1-メチル-2-[(フェニルスルファニル)メチル]-1H-インドール-3-カルボキシラート
  • 6-ブロモ-4-(ジメチルアミノメチル)-5-ヒドロキシ-1-メチル-2-[(フェニルチオ)メチル]-1H-インドール-3-カルボン酸メチル
  • エチル 6-ブロモ-4-[(ジメチルアミノ)メチル]-5-ヒドロキシ-1-メチル-2-[(フェニルスルファニル)メチル]-1H-インドール-3-カルボキシラート
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