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Velpatasvir

SKU: orb1226413

Description

Velpatasvir (GS-5816) is a second generation, pan-genotypic inhibitor of HCV NS5A, demonstrates a high barrier to resistance in HCV replicon assays.HCV Infection Phase 3 Clinical.

Images & Validation

Key Properties

CAS Number1377049-84-7
MW883.0018
Purity>98% (HPLC)
FormulaC49H54N8O8
SMILESO=C(OC)N[C@H](C1=CC=CC=C1)C(N2[C@H](C3=NC=C(C4=CC5=C(C6=CC7=CC=C8C(NC([C@H]9N(C([C@H](C(C)C)NC(OC)=O)=O)[C@@H](C)CC9)=N8)=C7C=C6OC5)C=C4)N3)C[C@H](COC)C2)=O
TargetHCV
SolubilityDMSO: 146.66 mg/mL (Need ultrasonic and warming)

Bioactivity

In Vivo
Animal model: CCl4-induced non-HCV rat model. Dosage: 10 mg/kg/d alone, or in combination with Sofosbuvir (20 mg/kg/d). Administration: p.o. Result: Decreased the levels of TNF-a, NF-κB and IL-6 in serum and hepatic tissues. Inhibited hepatic stellate cells (HSCs).

Storage & Handling

StorageStorage temperature: -20°C. Stability: ≥ 2 years
Expiration Date12 months from date of receipt.
DisclaimerFor research use only

Alternative Names

GS-5816 | GS 5816 | GS5816

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  • Velpatasvir [orb1304313]

    99.91% (May vary between batches)

    1377049-84-7

    883

    C49H54N8O8

    100 mg, 200 mg, 5 mg, 25 mg, 500 mg, 1 ml x 10 mM (in DMSO), 10 mg, 50 mg
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Protocol Information

Velpatasvir (orb1226413)

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(Recommended: An additional animal making an allowance for loss during the experiment)

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% DMSO +
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Available Sizes

Select a size below

500 mg
10 mg
$ 90.00
50 mg
$ 170.00
100 mg
$ 240.00
200 mg
$ 340.00