Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C32H35F3N4O5S |
| Molecular Weight | 644.704 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCS(=O)(=O)N1CCN(CC2=CC=C(NC(=O)C3=CC=C(C=C3)C4=C(OC(F)(F)F)C=CC(NC(=O)C5CC5)=C4)C=C2)CC1
InChI
InChIKey=MAQDQJWCSSCURR-UHFFFAOYSA-N
InChI=1S/C32H35F3N4O5S/c1-2-19-45(42,43)39-17-15-38(16-18-39)21-22-3-11-26(12-4-22)36-30(40)24-7-5-23(6-8-24)28-20-27(37-31(41)25-9-10-25)13-14-29(28)44-32(33,34)35/h3-8,11-14,20,25H,2,9-10,15-19,21H2,1H3,(H,36,40)(H,37,41)
A-689 (AZD-7295) was the lead compound from Arrow Therapeutics' second series of hepatitis C virus (HCV) NS5a inhibitors. AZD-7295 is a selective inhibitor of HCV NS5A within vitroantiviral activity of 7nM and 1.24mM against HCV genotype1b and 1a replicons respectively, with significant liver concentrationin preclinical studies. AZD-7295 was well tolerated at repeated doses ofup to 700 mg daily. AZD-7295 shows potent antiviral activity ingenotype 1b patients. Genotype 1a and genotype 3 patients showedno antiviral effects.
Originator
Approval Year
Sample Use Guides
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102MC1467J
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929890-64-2
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DB12724
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57339445
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AZD-7295
Created by
admin on Sat Dec 16 10:35:46 GMT 2023 , Edited by admin on Sat Dec 16 10:35:46 GMT 2023
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PRIMARY | Official Title:A Randomised, DB, PC Study to Determine the PK, Safety and Tolerability Profile and Antiviral Activity of Multiple Oral Doses of AZD7295 in Otherwise Healthy Male and Female Hepatitis C Carriers With Compensated Liver DiseasePurpose:PK, safety study of AZD7295 in HCV carriers |
ACTIVE MOIETY
