Sofosbuvir PSI-7977 GS-7977 Cas 1190307-88-0
Sofosbuvir PSI-7977 GS-7977 Cas 1190307-88-0
+ AII PRODUCTS
- Prostaglandins - Custom Synthesis - PARP Inhibitors - PI3K Inhibitors - FAK Inhibitors - AKT Inhibitors - C-Kit Inhibitors - VEGFR Inhibitors - c-Met Inhibitors - CDK Inhibitors - CYP17 Inhibitors - DNA/RNA Inhibitors - mTOR Inhibitors - SRC Inhibitors - Others
Product
|
Size |
Price |
Stock |
Quantity |
|---|---|---|---|
|
Get Quotation Now Add to Cart Bulk Inquiry |
|||
AddThis Sharing Buttons
Share to FacebookFacebookShare to TwitterTwitterShare to PrintPrintShare to EmailEmailShare to PinterestPinterestShare to GmailGmailShare to LinkedInLinkedInShare to Email AppEmail AppShare to TumblrTumblrShare to MoreAddThis
Shipping and handling fee USD40, Free delivery is qualified when the total value of your order exceeds USD500.If the item is temporarily out of stock. Please email to order@pharm-intermediates.com,we will inform you when we have it in stock.
Chemical Information
|
Product name:Sofosbuvir (PSI-7977, GS-7977) |
Purity:98% min |
|
CAS NO:1190307-88-0 |
Solubility:DMSO100 mg/mL (188.88 mM) |
|
Molecular Formula:C22H29FN3O9P |
Package:Packaging according to customer requirements. |
|
Molecular Weight:529.45 |
Storage:Store at -20℃ |
Quality control
COA
Remarks
Sofosbuvir (PSI-7977, GS-7977) is a HCVNS5B polymeraseinhibitor for the treatment of chronic hepatitis C virus (HCV) infection.
As HCV NS5B polymerase inhibitor, PSI-7977 displays more potent inhibitory activity against HCV RNA replication than PSI-7976 with EC50 of 92 nM versus 1.07 M and EC90 of 0.29 M versus 2.99 M, consistent with that incubating clone A cells with PSI-7977 leads to a higher concentration of PSI-7409 than clone A cells incubated with PSI-7976. PSI-7977 is an effective substrate for CatA to form PSI-352707 with 18-30 fold more potency as compared with PSI-7976. Unlike GS-7976, however, the CES1-mediated hydrolysis of PSI-7977 does not progress in a time-dependent manner.The S282T NS5B polymerase mutation but not S96T mutation confers resistance to PSI-7977 with EC90 increases from 0.42 M to 7.8 M. When assessed in an 8-day cytotoxicity assay, PSI-7977 displays no cytotoxicity against Huh7, HepG2, BxPC3, and CEM cells even at concentrations up to 100 M. PSI-7977 treatment for 14 days shows a IC90 of 72.1 M and 68.6 M for the inhibition of mtDNA and rDNA, respectively, in HepG2 cells.PSI-7977 exhibits potent activity against genotype (GT) 1a, 1b, and 2a (strain JFH-1) replicons and chimeric replicons containing GT 2a (strain J6), 2b, and 3a NS5B polymerase. Sequence analysis of the JFH-1 NS5B region indicates that additional amino acid changes including T179A, M289L, I293L, M434T, and H479P are selected both prior to and after the emergence of S282T, which are required to confer resistance to PSI-7977.
References
[1] Murakami E, et al. J Biol Chem, 2010, 285(45), 34337-34347.
[2] Sofia MJ, et al. J Med Chem, 2010, 53(19), 7202-7218.
[3] Lam AM, et al. Antimicrob Agents Chemother, 2012, 56(6),
Get in Touch
Have questions about our products or want to discuss a custom order? Our team is ready to help you.