rel-(3aR,5s,6aS)-N-(3-Methoxy-1,2,4-thiadiazol-5-yl)-5-(methyl(7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)hexahydrocyclopenta[c]pyrrole-2(1H)-carboxamide
98%
- Product Code: 231945
CAS:
1445987-21-2
Molecular Weight: | 414.49 g./mol | Molecular Formula: | C₁₈H₂₂N₈O₂S |
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EC Number: | MDL Number: | MFCD32701909 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Used in the pharmaceutical industry as an active ingredient in antiviral medications, particularly in treatments targeting RNA viruses. It functions as a nucleoside analog that interferes with viral replication by inhibiting key viral enzymes such as RNA-dependent RNA polymerase. Its structure allows efficient incorporation into viral RNA, leading to chain termination and suppression of viral load. Due to its targeted mechanism and metabolic stability, it is formulated in oral dosage forms for treating chronic viral infections. Also under investigation for broad-spectrum antiviral applications, including in emerging viral diseases.
Sizes / Availability / Pricing:
Size | Availability | Price | Quantity |
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0.010 | 10-20 days | $587.51 |
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0.025 | 10-20 days | $998.36 |
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0.050 | 10-20 days | $1,797.25 |
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0.100 | 10-20 days | $3,124.60 |
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rel-(3aR,5s,6aS)-N-(3-Methoxy-1,2,4-thiadiazol-5-yl)-5-(methyl(7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)hexahydrocyclopenta[c]pyrrole-2(1H)-carboxamide
Used in the pharmaceutical industry as an active ingredient in antiviral medications, particularly in treatments targeting RNA viruses. It functions as a nucleoside analog that interferes with viral replication by inhibiting key viral enzymes such as RNA-dependent RNA polymerase. Its structure allows efficient incorporation into viral RNA, leading to chain termination and suppression of viral load. Due to its targeted mechanism and metabolic stability, it is formulated in oral dosage forms for treating chronic viral infections. Also under investigation for broad-spectrum antiviral applications, including in emerging viral diseases.
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