Galidesivir triphosphate

Modify Date: 2025-08-25 17:48:39

Galidesivir triphosphate Structure
Galidesivir triphosphate structure
Common Name Galidesivir triphosphate
CAS Number 1467740-78-8 Molecular Weight 505.21
Density N/A Boiling Point N/A
Molecular Formula C11H18N5O12P3 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of Galidesivir triphosphate


Galidesivir triphosphate (Immucillin-A triphosphate) is converted by the prodrug Galidesivir. Galidesivir triphosphate is a substrate for viral RNA-dependent RNA polymerase (RDRP), resulting in termination of viral RNA replication and thus serves as an antiviral. Galidesivir triphosphate inhibits HCV NS5B RNA polymerase activity and protects mice against Ebola[1][2].

 Names

Name Galidesivir triphosphate

 Galidesivir triphosphate Biological Activity

Description Galidesivir triphosphate (Immucillin-A triphosphate) is converted by the prodrug Galidesivir. Galidesivir triphosphate is a substrate for viral RNA-dependent RNA polymerase (RDRP), resulting in termination of viral RNA replication and thus serves as an antiviral. Galidesivir triphosphate inhibits HCV NS5B RNA polymerase activity and protects mice against Ebola[1][2].
Related Catalog
In Vitro In virus-infected cells, Galidesivir is converted to the triphosphate, is incorporated into the viral transcript, and functions as an atypical chain-terminator for RNA-dependent RNA polymerases. Galidesivir is converted to the mono-, di-, and triphosphates in virus-infected human Huh-7 cells[1]. Galidesivir triphosphate (Immucillin-A triphosphate) (1-60 μM) inhibits hepatitis C virus (HCV) RNA polymerase transcriptional activity in a cell-free, isolated enzyme transcription assay.The triphosphate is a substrate for viral RNA-dependent RNA polymerase. Its incorporation permits the addition of a few additional encoded bases at which point the Galidesivir-modified RNA cannot be elongated[2].
In Vivo In vivo conversion of Galidesivir to its TP (Galidesivir triphosphate) nucleotide is particularly efficient[3]
References

[1]. Evans GB, et al. Immucillins in Infectious Diseases. ACS Infect Dis. 2018 Feb 9;4(2):107-117.

[2]. Warren TK, et al. Protection against filovirus diseases by a novel broad-spectrum nucleoside analogue BCX4430. Nature. 2014 Apr 17;508(7496):402-5.

[3]. Taylor R, et al. BCX4430 - A broad-spectrum antiviral adenosine nucleoside analog under development for the treatment of Ebola virus disease. J Infect Public Health. 2016 May-Jun;9(3):220-6.

 Chemical & Physical Properties

Molecular Formula C11H18N5O12P3
Molecular Weight 505.21
InChIKey NMSMIMMTMMGSHI-KUBHLMPHSA-N
SMILES Nc1ncnc2c(C3NC(COP(=O)(O)OP(=O)(O)OP(=O)(O)O)C(O)C3O)c[nH]c12
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