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Verification code

ACH-806

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Category Hepatitis C Virus (HCV)
CAS 870142-71-5
Description ACH-806 is a Hepatitis C virus NS3 protein inhibitor. It can inhibit viral RNA replication in HCV replicon cells and is active in genotype 1 HCV-infected patients in a proof-of-concept clinical trial. But Phase-II for Hepatitis C treatment was discontinued.
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Product Information

Synonyms ACH-806; ACH 806; ACH806; GS-9132; GS9132; GS 9132; N-(((4-(pentyloxy)-3-(trifluoromethyl)phenyl)amino)thioxomethyl)-3-Pyridinecarboxamide,
IUPAC Name N-[[4-pentoxy-3-(trifluoromethyl)phenyl]carbamothioyl]pyridine-3-carboxamide
Molecular Weight 411.45
Molecular Formula C19H20F3N3O2S
Canonical SMILES CCCCCOc1ccc(cc1C(F)(F)F)NC(=S)NC(=O)c2cccnc2
InChI 1S/C19H20F3N3O2S/c1-2-3-4-10-27-16-8-7-14(11-15(16)19(20,21)22)24-18(28)25-17(26)13-6-5-9-23-12-13/h5-9,11-12H,2-4,10H2,1H3,(H2,24,25,26,28)
InChIKey WJSGOXONRXFGRY-UHFFFAOYSA-N
Purity 98%
Solubility Soluble in DMSO
Appearance Powder
Application HCV
Shelf Life 2 month in rt, long time
Storage -20℃ Freezer
Assay Huh-luc/neo cells are seeded in 96-well plates at a density of 8,000 cells per well with a final volume of 200 μL supplemented with 10% fetal bovine serum with Dulbecco Modified Eagle medium (DMEM). ACH-806 is serially diluted in 100% dimethyl sulfoxide (DMSO) and added to the cells at a dilution of 1:200 to reach a final concentration of 0.5% DMSO at a total volume of 200 μL. Cells are quantified by measuring luciferase activity using a commercial kit.
Complexity 519
Exact Mass 411.12300
In Vitro ACH-806 is an NS4A antagonist that inhibits hepatitis C virus (HCV) replication at 14 nM for EC50. ACH-806 treatment results in a significant reduction in NS3 and NS4A in transfected cells.
PSA 105.87000
Target HCV Protease; HCV
XLogP3-AA 5.1

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