Viral polymerase-IN-1 hydrochloride

Modify Date: 2025-08-26 09:43:49

Viral polymerase-IN-1 hydrochloride Structure
Viral polymerase-IN-1 hydrochloride structure
Common Name Viral polymerase-IN-1 hydrochloride
CAS Number 2367587-02-6 Molecular Weight 419.77
Density N/A Boiling Point N/A
Molecular Formula C15H16ClF2N5O5 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of Viral polymerase-IN-1 hydrochloride


Viral polymerase-IN-1 hydrochloride, a Gemcitabine (HY-17026) derivative, potently inhibits influenza A and B viruses infection with IC90 values of 11.4-15.9 μM. Viral polymerase-IN-1 hydrochloride is active against SARS-CoV-2 infection. Viral polymerase-IN-1 hydrochloride suppresses influenza virus infection by affecting viral RNA replication/transcription in cells[1].

 Names

Name Viral polymerase-IN-1 hydrochloride

 Viral polymerase-IN-1 hydrochloride Biological Activity

Description Viral polymerase-IN-1 hydrochloride, a Gemcitabine (HY-17026) derivative, potently inhibits influenza A and B viruses infection with IC90 values of 11.4-15.9 μM. Viral polymerase-IN-1 hydrochloride is active against SARS-CoV-2 infection. Viral polymerase-IN-1 hydrochloride suppresses influenza virus infection by affecting viral RNA replication/transcription in cells[1].
Related Catalog
Target

IC50: 6.4 μM (H1N1) and 5.0 μM (H1N1)[1]

In Vitro Viral polymerase-IN-1 hydrochloride (化合物 2h; 0.1, 1, 10 μM; 过夜) 以剂量依赖性方式降低病毒 NP 蛋白表达和病毒 RNA 拷贝[1]。 Viral polymerase-IN-1 hydrochloride (11, 33, 100 μM; 72 小时) 以剂量依赖的方式有效抑制病毒聚合酶活性,从而抑制人细胞 HeLa 中甲型流感病毒 PR8 的聚合酶活性[1]。 Viral polymerase-IN-1 hydrochloride 有效抑制 SARS-CoV-2 感染,在 Calu-3 细胞中 EC50 值为 0.46 μM,CC50 值高于 100 μM,SI 值>217.4[1]。 Western Blot Analysis[1] Cell Line: MDCK cells infected PR8 virus Concentration: 0.1, 1, 10 μM Incubation Time: Overnight Result: Reduced viral NP protein expression and viral RNA copies in a dose-dependent manner.
In Vivo Viral polymerase-IN-1 hydrochloride (化合物 2h; 5 mg/kg; 腹腔给药; 每天一次; 持续 5 天; 在病毒感染前 4 小时开始) 不仅可以降低小鼠肺部的病毒 RNA 水平,还可以减轻感染介导的肺部浸润[1]。 Animal Model: Six-week-old BALB/c female mice intranasal infection with maPR8[1] Dosage: 5 mg/kg Administration: IP; once daily for 5 days, beginning 4 h prior to virus infection Result: Alleviated lung damage or reduced viral RNA replication.
References

[1]. Hyeon-Min Cha, et al. Evaluation of Antiviral Activity of Gemcitabine Derivatives against Influenza Virus and Severe Acute Respiratory Syndrome Coronavirus 2. ACS Infect Dis. 2023 Apr 14;9(4):1033-1045.  

 Chemical & Physical Properties

Molecular Formula C15H16ClF2N5O5
Molecular Weight 419.77
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.