Valganciclovir MedChemExpress (MCE)

Product Name	Valganciclovir hydrochloride
Synonyms	Valcyt Valcyte Rs 079070-194 Unii-4p3T9qf9nz VALGANCICLOVIR HCL Valganciclovir hydrochloride Valganciclovir hydrochloride hydrate Synonyms Valcyt Valcyte Rs 079070-194 Unii-4p3T9qf9nz VALGANCICLOVIR HCL Valganciclovir hydrochloride Valganciclovir hydrochloride hydrate L-VALINE,2-[(2-AMINO-1,6-DIHYDRO-6-OXO-9H-PURIN-9-YL)METHOXY]-3-HYDROXYPROPYLESTER,MONOHYDROCHLORIDE L-VALINE, 2-[(2-AMINO-1,6-DIHYDRO-6-OXO-9H-PURIN-9-YL)METHOXY]-3-HYDROXYPROPYL ESTER, MONOHYDROCHLORIDE L-Valine, 2-[(2-amino-1,6-dihydro-6-oxo-9H-purin-9-yl)methoxy]-3-hydroxypropyl ester, monohydrochloride hydrate 2-[(2-amino-6-oxo-6,9-dihydro-3H-purin-9-yl)methoxy]-3-hydroxypropyl (2S)-2-amino-3-methylbutanoate hydrochloride hydrate
CAS	175865-59-5
EINECS	641-360-4
Chemical Formula	C14H23ClN6O5
Molecular Weight	390.82
inchi	InChI=1/C14H22N6O5.ClH/c1-7(2)9(15)13(23)24-4-8(3-21)25-6-20-5-17-10-11(20)18-14(16)19-12(10)22;/h5,7-9,21H,3-4,6,15H2,1-2H3,(H3,16,18,19,22);1H/t8?,9-;/m0./s1
Package	10 mM * 1 mL;5 mg;10 mg;25 mg;50 mg;100 mg;200 mg;500 mg
Price	Email to quote
Descriptions	Valganciclovir hydrochloride Valganciclovir hydrochloride MedChemExpress (MCE) HY-A0032A 175865-59-5 98.0% 4°C, sealed storage, away from moisture In solvent : -80°C, 6 months Descriptions Valganciclovir hydrochloride Valganciclovir hydrochloride MedChemExpress (MCE) HY-A0032A 175865-59-5 98.0% 4°C, sealed storage, away from moisture In solvent : -80°C, 6 months -20°C, 1 month (sealed storage, away from moisture) Room temperature in continental US may vary elsewhere. Valganciclovir hydrochloride is an orally active antiviral agent. Valganciclovir hydrochloride can inhibit the growth of adenoviruses and have a protective effect on immunosuppressed hamsters. Valganciclovir hydrochloride can be used for the research of Cytomegalovirus. Valganciclovir (500 μM, 5-7 days) inhibits the growth of human adenoviruses (Ads) in A549 cells[1]. Valganciclovir (0.003-10 mM, 10 min) with ganciclovir (HY-13637) inhibits the uptake of glycylsarcosine in Caco-2 cells[2]. Valganciclovir (200 mg/kg, Oral gavage, twice daily for16 days) protects immunosuppressed hamsters challenged intravenously with adenovirus type 5 (Ad5)[1]. \| \| \| \| \| \| \| \| \| \| [1]. Toth K, et al. Valganciclovir inhibits human adenovirus replication and pathology in permissive immunosuppressed female and male Syrian hamsters [J]. Viruses, 2015, 7(3): 1409-1428. [Content Brief] [2]. Sugawara M, et al. Transport of valganciclovir, a ganciclovir prodrug, via peptide transporters PEPT1 and PEPT2 [J]. Journal of pharmaceutical sciences, 2000, 89(6): 781-789. [Content Brief] [3]. Cvetkovic R S, et al. Valganciclovir: a review of its use in the management of CMV infection and disease in immunocompromised patients [J]. Drugs, 2005, 65: 859-878. [Content Brief]
Last Update	2025-04-01 14:45:47

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