Strongly Inhibits Cat FIPV GS-441524 20mg/ML Purity
Basic Properties
Model Number:
GS-441524
Trading Properties
Minimum Order Quantity:
10 vials
Price:
Negotiable
Payment Terms:
L/C,D/A,D/P,T/T,Western Union
Supply Ability:
100000 vials per month
Specifications
| Function: | Cat FIPV | CAS: | 1191237-69-0 |
| Purity: | 20mg/mL | Test Method: | HPLC UV |
| Storage: | Cool Dry Place | Shipping Method: | Air(UPS, FedEx, TNT, EMS) Or Sea |
| MF: | C12H13N5O4 | Density: | 1.74-1.94 G/cm3 |
| Highlight: | Fip Drugs For Cats, Cat FIPV GS-441524, Strongly Inhibits GS-441524 |
Product Description
Gallery
Strongly Inhibits Cat FIPV GS-441524 20mg/ML Purity


Strongly Inhibits Cat FIPV GS-441524 With Fast Delivery
Product Description
This medicine is an adenosine nucleotide analog antiviral, similar to remdesivi.This molecule was patented in 2009. In vitro studies of GS have determined it has a higher EC50 than remdesivi against a number of viruses, meaning GS is less potent.This medicine continues to be studied in the treatment of Feline Infectious Peritonitis Virus, that only infects cats.
| Appearance | Transparent liquid, powder or tablets |
| GS Standard | 99.5%min |
| Size | 5.5 ml/ Vial |
| Content | 15mg/ml or 20mg/ml |
| Application | For CAT FIP R&D Use ONLY |
| Wet FIP | 6-7 mg/kg |
| Dry FIP | 7-8 mg/kg |
| Ocular or Neuro FIP | 8 mg/kg |
| Increased ocular/neuro | 9 mg/kg |
| Max ocular/neuro | 10 mg/kg |
GS-441524 nucleoside is phosphorylated with the aid of using nucleoside kinases (likely adenosine kinase (ADK), that is the enzyme that phosphorylates the structurally comparable ribavirin), after which phosphorylated once more with the aid of using nucleoside-diphosphate kinase (NDK) to the energetic nucleotide triphosphate form. The triphosphate of GS-441524, GS-443902, is likewise the bioactive anti-viral agent generated with the aid of using remdesivir, however is generated with the aid of using a extraordinary biochemical mechanism from the later.
Intracellular triple-phosphorylation of GS-441524 yields its energetic 1'-cyano-substituted adenosine triphosphate analogue, which immediately disrupts viral RNA replication with the aid of using competing with endogenous NTPs for incorporation into nascent viral RNA transcripts and triggering not on time chain termination of RNA-structured RNA polymerase.