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1383450-81-4
  • names:

    JNJ-678

  • CAS號:

    1383450-81-4

    MDL Number: MFCD30489307
  • MF(分子式): C21H20ClF3N4O3S MW(分子量): 500.92
  • EINECS:No data available Reaxys Number:No data available
  • Pubchem ID:118892432 Brand:BIOFOUNT
JNJ-678
JNJ-678 (1383450-81-4,JNJ-53718678) 是新型融合蛋白 (fusion protein) 抑制劑,有潛力用于呼吸道合胞病毒 (RSV)的研究。
貨品編碼 規(guī)格 純度 價格 (¥) 現(xiàn)價(¥) 特價(¥) 庫存描述 數(shù)量 總計 (¥)
YZM000872-10mg 10mg 98% ¥ 7594.00 ¥ 7594.00 2-3天
- +
0.00
YZM000872-5mg 5mg 98% ¥ 4488.00 ¥ 4488.00 2-3天
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0.00
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中文別名 JNJ-678(1383450-81-4);JNJ-53718678;Rilematovir
英文別名 JNJ-678(1383450-81-4)
CAS號 1383450-81-4
Inchi InChI=1S/C21H20ClF3N4O3S/c1-33(31,32)8-2-7-27-16(10-14-9-15(22)3-4-17(14)27)12-28-19-11-26-6-5-18(19)29(20(28)30)13-21(23,24)25/h3-6,9-11H,2,7-8,12-13H2,1H3
InchiKey GTQTUABHRCWVLL-UHFFFAOYSA-N
分子式 Formula C21H20ClF3N4O3S
分子量 Molecular Weight 500.92
溶解度Solubility 生物體外In Vitro:DMSO溶解度65 mg/mL(129.76 mM;Need ultrasonic)H2O< 0.1 mg/mL(insoluble)
性狀 白色至灰白色固體粉末
儲藏條件 Storage conditions -20°C 3 years年 4°C 2 years年 / 溶液中:-80°C 6 months月 -20°C 1 month月

JNJ-678 (1383450-81-4,JNJ-53718678)實驗注意事項:
1.實驗前需戴好防護眼鏡,穿戴防護服和口罩,佩戴手套,避免與皮膚接觸。
2.實驗過程中如遇到有毒或者刺激性物質及有害物質產生,必要時實驗操作需要手套箱內完成以免對實驗人員造成傷害
3.實驗后產生的廢棄物需分類存儲,并交于專業(yè)生物廢氣物處理公司處理,以免造成環(huán)境污染

JNJ-678 (1383450-81-4,JNJ-53718678) Experimental considerations:
1. Wear protective glasses, protective clothing and masks, gloves, and avoid contact with the skin during the experiment.
2. The waste generated after the experiment needs to be stored separately, and handed over to a professional biological waste gas treatment company to avoid environmental pollution.

Tag:JNJ-678 (1383450-81-4,JNJ-53718678),NJ-678試劑,NJ-678抑制劑,NJ-678的生產,NJ-678的純度,NJ-678的作用,NJ-678的含量,NJ-678的使用,NJ-678的合成,NJ-678的MSDS,NJ-678的價格,NJ-678的外觀,NJ-678的溶解度
產品說明 JNJ-678 (1383450-81-4,JNJ-53718678) 是新型融合蛋白的抑制劑,臨床試驗中用于治療呼吸道合胞病毒 (RSV)
IntroductionJNJ-678 (1383450-81-4,JNJ-53718678) is a novelfusion proteininhibitor in clinical trials for the treatment of respiratory syncytial virus (RSV).
Application1
Application2
Application3
Advances in respiratory virus therapeutics - A meeting report from the 6th isirv Antiviral Group conference PMID 30974127; Antiviral research 2019 07; 167(?):45-67 (Review Article)
Integrating Duodenal Sampling in a Human Mass Balance Study to Quantify the Elimination Pathways of JNJ-53718678, a Respiratory Syncytial Virus Fusion Protein Inhibitor PMID 31832988;
A human challenge model for respiratory syncytial virus kinetics, the pharmacological effect of a novel fusion inhibitor, and the modelling of symptoms scores
Therapeutic efficacy of a respiratory syncytial virus fusion inhibitor PMID 28761099; Nature communications 2017 08; 8(1):167
Advances in respiratory virus therapeutics - A meeting report from the 6th isirv Antiviral Group conference PMID 30974127; Antiviral research 2019 07; 167(?):45-67 (Review Article)
Therapeutic efficacy of a respiratory syncytial virus fusion inhibitor
Abstract:
Respiratory syncytial virus is a major cause of acute lower respiratory tract infection in young children, immunocompromised adults, and the elderly. Intervention with small-molecule antivirals specific for respiratory syncytial virus presents an important therapeutic opportunity, but no such compounds are approved today. Here we report the structure of JNJ-53718678 bound to respiratory syncytial virus fusion (F) protein in its prefusion conformation, and we show that the potent nanomolar activity of JNJ-53718678, as well as the preliminary structure-activity relationship and the pharmaceutical optimization strategy of the series, are consistent with the binding mode of JNJ-53718678 and other respiratory syncytial virus fusion inhibitors. Oral treatment of neonatal lambs with JNJ-53718678, or with an equally active close analog, efficiently inhibits established acute lower respiratory tract infection in the animals, even when treatment is delayed until external signs of respiratory syncytial virus illness have become visible. Together, these data suggest that JNJ-53718678 is a promising candidate for further development as a potential therapeutic in patients at risk to develop respiratory syncytial virus acute lower respiratory tract infection.Respiratory syncytial virus causes lung infections in children, immunocompromised adults, and in the elderly. Here the authors show that a chemical inhibitor to a viral fusion protein is effective in reducing viral titre and ameliorating infection in rodents and neonatal lambs.
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