ChemicalBook--->CAS DataBase List--->222631-44-9

222631-44-9

222631-44-9 Structure

222631-44-9 Structure
IdentificationBack Directory
[Name]

3,4-Pyrrolidinediol, 2-(4-amino-5H-pyrrolo3,2-dpyrimidin-7-yl)-5-(hydroxymethyl)-, monohydrochloride, (2S,3S,4R,5R)-
[CAS]

222631-44-9
[Synonyms]

BCX 4430
Galidesivir)
Galidesivir HCl
BCX-4430 (BCX4430
BCX4430;GALIDESIVIR
BCX 4430 hydrochloride
Galidesivir hydrochloride
Immucillin-A hydrochloride
GALIDESIVIR HYDROCHLORIDE (BCX 4430 HYDROCHLORIDE)
(2S,3S,4R,5R)-2-(4-Amino-5H-pyrrolo[3,2-d]pyrimidin-7-yl)-5-(hydroxymethyl)-3,4-pyrrolidinediol monohydrochloride
3,4-Pyrrolidinediol, 2-(4-amino-5H-pyrrolo3,2-dpyrimidin-7-yl)-5-(hydroxymethyl)-, monohydrochloride, (2S,3S,4R,5R)-
3,4-Pyrrolidinediol,2-(4-aMino-5H-pyrrolo[3,2-d]pyriMidin-7-yl)-5-(hydroxyMethyl)-, hydrochloride(1:1), (2S,3S,4R,5R)-
[Molecular Formula]

C11H16ClN5O3
[MOL File]

222631-44-9.mol
[Molecular Weight]

301.73
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

H2O: 2 mg/mL, clear
[form ]

Solid
[color ]

White to off-white
[Water Solubility ]

Water : ≥ 41 mg/mL (135.88 mM)
Hazard InformationBack Directory
[Uses]

BCX 4430 is an antiviral drug, an adenosine analog). It is developed by BioCryst Pharmaceuticals with funding from NIAID, originally intended as a treatment for Hepatitis C, but subsequently developed as a potential treatment for deadly filovirus infections such as Ebola virus disease and Marburg virus disease.
[in vivo]

Galidesivir (BCX4430) hydrochloride is active after intramuscular, intraperitoneal, and oral administration in a variety of experimental infections. In nonclinical studies involving lethal infections with Ebola virus, Marburg virus, Rift Valley fever virus, and Yellow Fever virus, Galidesivir hydrochloride has demonstrated pronounced efficacy[1].
Galidesivir hydrochloride (4 mg/kg; i.p.; twice daily for 7 days) is effectively in a hamster model of yellow fever (YF)[4].

Animal Model:Female Syrian golden hamsters (hamsters infected with YF virus)[4]
Dosage:4 mg/kg of body weight
Administration:I.p.; twice daily for 7 days
Result:Significantly improved the survival of hamsters infected with YFV.
[storage]

Store at -20°C
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