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Lagociclovir

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Category Hepatitis B Virus (HBV)
CAS 92562-88-4
Description Lagociclovir is a prodrug of 3'-fluoro-2',3'-dideoxyguanosine with high oral bioavailability in humans and potent activity against HBV.
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Product Information

Synonyms MIV-210; MIV 210; MIV210; 3'-FddG; Fddguo; Lagociclovir.
IUPAC Name 2-amino-9-[(2R,4S,5R)-4-fluoro-5-(hydroxymethyl)oxolan-2-yl]-1H-purin-6-one
Molecular Weight 269.23
Molecular Formula C10H12FN5O3
Canonical SMILES C1C(C(OC1N2C=NC3=C2NC(=NC3=O)N)CO)F
InChI InChI=1S/C10H12FN5O3/c11-4-1-6(19-5(4)2-17)16-3-13-7-8(16)14-10(12)15-9(7)18/h3-6,17H,1-2H2,(H3,12,14,15,18)/t4-,5+,6+/m0/s1
InChIKey RTJUXLYUUDBAJN-KVQBGUIXSA-N
Boiling Point 633.5±65.0 °C at 760 mmHg
Flash Point 336.9±34.3 °C
Purity >98%
Density 2.0±0.1 g/cm3
Solubility In vitro:
10 mM in DMSO
Appearance Solid powder
Application Antiviral Agents
Storage Store at -20°C
Complexity 420
Exact Mass 269.09241742
Index Of Refraction 1.834
In Vitro Oral administration of MIV-210 at 20 or 60 mg/kg of body weight/day induced a rapid virological response in chronically infected woodchucks, reducing serum WHV DNA levels by 4.75 log10 and 5.72 log10, respectively, in 2 weeks. Further, a daily dose of 10 mg/kg decreased the serum WHV load 400-fold after 4 weeks of treatment, and a dose of 5 mg/kg/day was sufficient to maintain this antiviral effect during the following week period. MIV-210 at 20 or 60 mg/kg/day reduced the liver WHV DNA load 200- to 2,500-fold from pretreatment levels and, importantly, led to a 2.0 log10 drop in the hepatic content of WHV covalently closed circular DNA.
PSA 119.05000
Target HBV
Vapor Pressure 0.0±2.0 mmHg at 25°C
XLogP3-AA -0.9

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