Cidofovir dihydrate
CAS No. 149394-66-1
Cidofovir dihydrate( HPMPC dihydrate | (S)-HPMPC dihydrate )
Catalog No. M12069 CAS No. 149394-66-1
The prodrug of cidofovir diphosphate that inhibits cytomegalovirus (CMV) viral replication by selectively inhibiting viral DNA polymerases.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 45 | Get Quote |
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| 10MG | 68 | Get Quote |
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| 25MG | 115 | Get Quote |
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| 50MG | 173 | Get Quote |
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| 100MG | 258 | Get Quote |
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| 200MG | 388 | Get Quote |
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| 500MG | Get Quote | Get Quote |
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| 1G | Get Quote | Get Quote |
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Biological Information
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Product NameCidofovir dihydrate
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NoteResearch use only, not for human use.
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Brief DescriptionThe prodrug of cidofovir diphosphate that inhibits cytomegalovirus (CMV) viral replication by selectively inhibiting viral DNA polymerases.
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DescriptionThe prodrug of cidofovir diphosphate that inhibits cytomegalovirus (CMV) viral replication by selectively inhibiting viral DNA polymerases; also incorporates itself into viral DNA hence inhibiting viral DNA synthesis during reproduction.CMV Infection Approved.
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In VitroCidofovir (5-100 μM, 72 hours) dihydrate has antiviral activity against feline herpesvirus type-1 (FHV-1) with an IC50 of 11 μM, and can reduce Crandell-Reese feline kidney cells counts in a dose dependent manner. Cidofovir (10-1000 μM, 24-120 hours) dihydrate can reduce cancer cell viability and induces apoptosis.Cell Cytotoxicity Assay Cell Line:Crandell-Reese feline kidney(CRFK) cellsConcentration:10-100 μM Incubation Time:72 hours Result:Reduced CRFK cells by 9.1%.Cell Viability Assay Cell Line:Caco-2, FTC-133, HeLa, Hep-G2, MDA-MB-231, NCI-H1975 and PC-3 cells Concentration:10-1000 μM Incubation Time:24, 48, 72, 96, 120 hours Result:Resulted in a gradual decrease in tumor cell viability with time and concentration increasing and inhibited the number of FTC-133 cell clones by about 55% at 100 μM comparing to the untreated group.Apoptosis Analysis Cell Line:FTC-133 cells Concentration:100 μM Incubation Time:96 hours Result:Showed a significant increase in the expression of pro-apoptotic proteins, such as cytochrome c, phospho-p53 (S15) and caspase-3 by 130%, 49%, and 46%, respectively while the anti-apoptotic protein Bcl-x decreased significantly by 57% comparing to the untreated cells.
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In VivoCidofovir (subcutaneous injection, 100 mg/kg, 3-6 days interval, 21 days)dihydrate is highly protective against death from cowpox virus (CPV) infection at high doses in female weanling BALB/c mice. Animal Model:Female weanling BALB/c mice infected with cowpox virus (CPV)Dosage:100 mg/kg Administration:Subcutaneous injection; 3-6 days interval; 21 days Result:Prevented 80-100% of mouse deaths when administered on the first 4-3 days before infection.Protected 35-50% of mice when administered on the fourth day after infection, and 10-20% when administered on the sixth day.
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SynonymsHPMPC dihydrate | (S)-HPMPC dihydrate
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PathwayMicrobiology/Virology
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TargetCMV
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RecptorCMV
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Research AreaInfection
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IndicationCMV Infection
Chemical Information
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CAS Number149394-66-1
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Formula Weight315.2176
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Molecular FormulaC8H18N3O8P
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Purity>98% (HPLC)
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Solubility10 mM in DMSO
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SMILESC1=CN(C(=O)N=C1N)CC(CO)OCP(=O)(O)O.O.O
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Chemical NamePhosphonic acid, P-[[(1S)-2-(4-amino-2-oxo-1(2H)-pyrimidinyl)-1-(hydroxymethyl)ethoxy]methyl]-, hydrate (1:2)
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
molnova catalog
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