Home Microbiology HIV Protease inhibitor - HBV inhibitor - HCV Protease inhibitor Azvudine For research use only.

Azvudine

Synonyms: RO-0622

Azvudine (RO-0622) is a novel nucleoside reverse transcriptase inhibitor with antiviral activity against human immunodeficiency virus (HIV), hepatitis B virus (HBV) and hepatitis C virus (HCV), potently inhibits HIV-1 (EC50 range 0.03 to 6.92 nM) and HIV-2 (EC50s ranging from 0.018 to 0.025 nM).

Azvudine Chemical Structure

Azvudine Chemical Structure

CAS No. 1011529-10-4

Purity & Quality Control

Batch: E124301 DMSO]57 mg/mL]false]Water]57 mg/mL]false]Ethanol]57 mg/mL]false Purity: 99.86%
99.86

Azvudine Related Products

Signaling Pathway

HIV Protease Signaling Pathways

HIV Protease Signaling Pathway

Biological Activity

Description Azvudine (RO-0622) is a novel nucleoside reverse transcriptase inhibitor with antiviral activity against human immunodeficiency virus (HIV), hepatitis B virus (HBV) and hepatitis C virus (HCV), potently inhibits HIV-1 (EC50 range 0.03 to 6.92 nM) and HIV-2 (EC50s ranging from 0.018 to 0.025 nM).
Targets
HIV-1 [1]
(in antiviral activity assays)		 HIV-2 [1]
(in antiviral activity assays)		 HBV [1] HCV [1]
0.03~ 6.92 nM(EC50) 0.018~ 0.025 nM(EC50)
NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT05689034 Not yet recruiting
COVID-19 Respiratory Infection
Peking Union Medical College Hospital
 January 20 2023 Phase 2|Phase 3
NCT05033145 Completed
COVID-19
HRH Pharmaceuticals Limited|GALZU INSTITUTE OF RESEARCH TEACHING SCIENCE AND APPLIED TECHNOLOGY Brazil|Clinical Research Unit / High Complexity Center (CRU/HCC) / Galzu Institute
 January 15 2022 Phase 3
NCT04668235 Completed
COVID-19
HRH Pharmaceuticals Limited|GALZU INSTITUTE OF RESEARCH TEACHING SCIENCE AND APPLIED TECHNOLOGY Brazil|UNIVERSIDADE ESTADUAL DO NORTE FLUMINENSE (UENF) Brazil
 April 23 2021 Phase 3

Chemical Information & Solubility

Molecular Weight 286.22 Formula

C9H11FN6O4
CAS No. 1011529-10-4 SDF --
Storage (From the date of receipt) 3 years -20°C powder

In vitro
Batch:

DMSO : 57 mg/mL ( (199.14 mM) Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)

Water : 57 mg/mL

Ethanol : 57 mg/mL


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In vivo
Batch:

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In vivo Formulation Calculator

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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such
as vortex, ultrasound or hot water bath can be used to aid dissolving.

Tech Support

Answers to questions you may have can be found in the inhibitor handling instructions. Topics include how to prepare stock solutions, how to store inhibitors, and issues that need special attention for cell-based assays and animal experiments.

Handling Instructions

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