Cidofovir Dihydrate

Modify Date: 2024-01-04 16:01:15

Cidofovir Dihydrate Structure
Cidofovir Dihydrate structure
Common Name Cidofovir Dihydrate
CAS Number 149394-66-1 Molecular Weight 315.22
Density 1.8±0.1 g/cm3 Boiling Point 609.5±65.0 °C at 760 mmHg
Molecular Formula C8H18N3O8P Melting Point 260ºC (dec)
MSDS N/A Flash Point 322.4±34.3 °C

 Use of Cidofovir Dihydrate


Cidofovir dehydrate is an injectable antiviral medication for the treatment of cytomegalovirus (CMV) retinitis, which suppresses virus replication by selective inhibition of viral DNA synthesis.Target: CMV DNA polymeraseCidofovir is an injectable antiviral medication for the treatment of cytomegalovirus (CMV) retinitis in patients with AIDS. It suppresses CMV replication by selective inhibition of viral DNA polymerase and therefore prevention of viral replication and transcription. It is an acyclic nucleoside phosphonate, and is therefore independent of phosphorylation by viral enzymes, unlike acyclovir.Cidofovir was discovered at the Institute of Organic Chemistry and Biochemistry, Prague, by Antonín Hol?, and developed by Gilead Sciences and is marketed with the brand name Vistide by Gilead in the USA, and by Pfizer elsewhere. Maintenance therapy with cidofovir involves an infusion only once every two weeks, making it a convenient treatment option. Because dosing is relatively infrequent, a permanent catheter is not necessary for infusions.

 Names

Name cidofovir dihydrate
Synonym More Synonyms

 Cidofovir Dihydrate Biological Activity

Description Cidofovir dehydrate is an injectable antiviral medication for the treatment of cytomegalovirus (CMV) retinitis, which suppresses virus replication by selective inhibition of viral DNA synthesis.Target: CMV DNA polymeraseCidofovir is an injectable antiviral medication for the treatment of cytomegalovirus (CMV) retinitis in patients with AIDS. It suppresses CMV replication by selective inhibition of viral DNA polymerase and therefore prevention of viral replication and transcription. It is an acyclic nucleoside phosphonate, and is therefore independent of phosphorylation by viral enzymes, unlike acyclovir.Cidofovir was discovered at the Institute of Organic Chemistry and Biochemistry, Prague, by Antonín Hol?, and developed by Gilead Sciences and is marketed with the brand name Vistide by Gilead in the USA, and by Pfizer elsewhere. Maintenance therapy with cidofovir involves an infusion only once every two weeks, making it a convenient treatment option. Because dosing is relatively infrequent, a permanent catheter is not necessary for infusions.
Related Catalog
References

[1]. Becker MN, et al. Isolation and characterization of cidofovir resistant vaccinia viruses. Virol J. 2008 May 14;5:58.

[2]. Kazory A, et al. Simultaneous development of Fanconi syndrome and acute renal failure associated with cidofovir. J Antimicrob Chemother. 2007 Jul;60(1):193-4. Epub 2007 May 11.

[3]. Segarra-Newnham M, et al. Use of cidofovir in progressive multifocal leukoencephalopathy. Ann Pharmacother. 2001 Jun;35(6):741-4.

 Chemical & Physical Properties

Density 1.8±0.1 g/cm3
Boiling Point 609.5±65.0 °C at 760 mmHg
Melting Point 260ºC (dec)
Molecular Formula C8H18N3O8P
Molecular Weight 315.22
Flash Point 322.4±34.3 °C
PSA 157.71000
LogP -3.37
Vapour Pressure 0.0±4.0 mmHg at 25°C
Index of Refraction 1.656

 Synonyms

Cidofovir hydrate (1:2)
Gs-0504
Phosphonic acid, [[(1S)-2-(4-amino-2-oxo-1(2H)-pyrimidinyl)-1-(hydroxymethyl)ethoxy]methyl]-
Cidofovir dihydrate
({[(2S)-1-(4-Amino-2-oxopyrimidin-1(2H)-yl)-3-hydroxypropan-2-yl]oxy}methyl)phosphonic acid
Cidofovir
(S)-[[2-(4-Amino-2-oxo-1(2H)-pyrimidinyl)-1-(hydroxymethyl)ethoxy]methyl]phosphonic Acid
Unii-jil713Q00n
(S)-HPMPC Hydrate
Cidovir Hydrate
Vistide Hydrate
(S)-2-(4-Amino-2-oxo-1(2H)-pyrimidinyl-1-(hydroxymethyl)ethoxy)methyl phosphonic acid
({[(2S)-1-(4-Amino-2-oxo-1(2H)-pyrimidinyl)-3-hydroxy-2-propanyl]oxy}methyl)phosphonic acid
Vistide
Drg-0145
Cidofovir hydrate
GS 0504 Hydrate
Cidofovir (dihydrate)
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