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Valganciclovir hydrochloride
CAS No. 175865-59-5
Valganciclovir hydrochloride( Ro 107-9070/194 | Valcyte )
Catalog No. M12657 CAS No. 175865-59-5
Valganciclovir (hydrochloride), the L-valyl ester of ganciclovir, is actually a prodrug for ganciclovir.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 30 | In Stock |
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| 10MG | 29 | In Stock |
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| 25MG | 51 | In Stock |
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| 50MG | 83 | In Stock |
|
| 100MG | 129 | In Stock |
|
| 200MG | 184 | In Stock |
|
| 500MG | 323 | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameValganciclovir hydrochloride
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NoteResearch use only, not for human use.
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Brief DescriptionValganciclovir (hydrochloride), the L-valyl ester of ganciclovir, is actually a prodrug for ganciclovir.
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DescriptionValganciclovir (hydrochloride), the L-valyl ester of ganciclovir, is actually a prodrug for ganciclovir. Valganciclovir is an antiviral medication used to treat cytomegalovirus infections.
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In VitroCell Viability Assay Cell Line:A549 cells Concentration:500 μM Incubation Time:5 days, 7days Result:Showed EC50 values ranged from 120.5 μM (Ad4) to 244.4 μM (Ad6).Showed IC50 values was calculated to be 11.74 mM at 7 days post-infection.
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In VivoAnimal Model:Immunosuppressed hamstersDosage:200 mg/kg Administration:Oral gavage (p.o.)Result:Resulted in significantly smaller magnitude of weight loss for all groups.Reduced the liver pathology.
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SynonymsRo 107-9070/194 | Valcyte
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PathwayOthers
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TargetOther Targets
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RecptorCMV
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Research AreaInfection
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Indication——
Chemical Information
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CAS Number175865-59-5
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Formula Weight390.82
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Molecular FormulaC14H23ClN6O5
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Purity>98% (HPLC)
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SolubilityWater: 78 mg/mL (199.58 mM); DMSO: 78 mg/mL (199.58 mM)
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SMILESCC(C)[C@H](N)C(OCC(OCN1C=NC2=C1NC(N)=NC2=O)CO)=O.[H]Cl
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Chemical Name[2-[(2-amino-6-oxo-3H-purin-9-yl)methoxy]-3-hydroxypropyl] (2S)-2-amino-3-methylbutanoate hydrochloride
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Sugawara M, et al. J Pharm Sci, 2000, 89(6), 781-789.
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