Antiviral

Antivirals are drugs that inhibit viral infection, targeting virus entry, assembly or replication. Mechanisms of antiviral action include blocking virus replication at key points, such as interfering with DNA polymerization or protease inhibition. They are used to treat viral infections such as HIV and CMV.

Products for Antiviral - Page 4

  1. Cat.No. Product Name Information/Activity
  2. BCN5893 Rosmarinic acid Rosmarinic acid is a widespread phenolic ester compound in the plants. Rosmarinic acid inhibits MAO-A, MAO-B and COMT enzymes with IC50s of 50.1, 184.6 and 26.7 μM, respectively. Rosmarinic acid chemical structure
  3. BCC7460 RWJ 21757 Loxoribine (7-Allyl-8-oxoguanosine) is a guanosine analog with anti-viral and anti-tumor activities. Loxoribine is an orally bioavailable and selective Toll-like receptor (TLR) 7 agonist. RWJ 21757 chemical structure
  4. BCC5028 Stavudine (d4T) Stavudine is a nucleoside analog that inhibits reverse transcriptase and has in vitro activity against HIV. Stavudine (d4T) chemical structure
  5. BCC7079 Suramin hexasodium salt Suramin sodium salt (Suramin hexasodium salt) is a reversible and competitive protein-tyrosine phosphatases (PTPases) inhibitor. Suramin sodium salt is a potent inhibitor of sirtuins: SirT1 (IC50=297 nM), SirT2 (IC50=1.15 μM), and SirT5 (IC50=22 μM). Suramin sodium salt is a competitive inhibitor of reverse transcriptase (DNA topoisomerase II: IC50=5 μM). Suramin sodium salt is an antitrypanosomal, anti-neoplastic and anti-angiogenic agent. Suramin hexasodium salt chemical structure
  6. BCC2500 Tenofovir Tenofovir (GS 1278) is a nucleotide reverse transcriptase inhibitor to treat HIV and chronic Hepatitis B (HBV). Tenofovir chemical structure
  7. BCC2417 WR 1065 WR-1065 dihydrochloride can protect normal tissues from the toxic effects of certain cancer drugs and activate p53 through a JNK-dependent signaling pathway. WR 1065 chemical structure

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