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461443-59-4

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461443-59-4 Structure

461443-59-4 Structure
IdentificationBack Directory
[Name]

Aplaviroc
[CAS]

461443-59-4
[Synonyms]

AK 602
ONO 4128
Aplaviroc
GW 873140
GSK 873140
GWNOTCOIYUNTQP-FQLXRVMXSA-N
AK 602; AK-602; GW 873140; GW873140; ONO 4128
4-[4-[[(3R)-1-Butyl-3-[(R)-cyclohexylhydroxymethyl]-2,5-dioxo-1,4,9-triazaspiro[5.5]undec-9-yl]methyl]phenoxy]benzoic acid
Benzoic acid, 4-[4-[[(3R)-1-butyl-3-[(R)-cyclohexylhydroxymethyl]-2,5-dioxo-1,4,9-triazaspiro[5.5]undec-9-yl]methyl]phenoxy]-
[Molecular Formula]

C33H43N3O6
[MDL Number]

MFCD22200785
[MOL File]

461443-59-4.mol
[Molecular Weight]

577.71
Chemical PropertiesBack Directory
[Boiling point ]

800.6±65.0 °C(Predicted)
[density ]

1.29
[storage temp. ]

Store at -20°C
[solubility ]

Soluble in DMSO
[pka]

4.29±0.10(Predicted)
Hazard InformationBack Directory
[Uses]

Treatment of HIV infection.
[in vivo]

The concentration of Aplaviroc (AK602) reached the maximal concentration immediately after intraperitoneal administration and decreased rapidly[2].
Aplaviroc (AK602, 60 mg/kg, bid, daily) suppresses R5 HIV-1 viremia in hu-PBMC-NOG mice[2].

Animal Model:hu-PBMC-NOG mice[2].
Dosage:60 mg/kg.
Administration:Single intraperitoneal administration, bid, daily.
Result:The numbers of CD4+ cells/μL in saline-treated mice were significantly less than those of AK602-treated, ddI-treated, or uninfected mice.
[IC 50]

HIV-1Ba-L: 0.4 nM (IC50); HIV-1JRFL: 0.1 nM (IC50); HIV-1MOKW: 0.2 nM (IC50); CCR5
Spectrum DetailBack Directory
[Spectrum Detail]

Aplaviroc(461443-59-4)1HNMR
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