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Search Results for " virus replication "

20

Compounds

Cat No. Product Name Synonyms Targets
TN2283 Tripterifordin HIV Protease
Tripterifordin shows anti-HIV replication activity in H9 lymphocyte cells with an EC50 of 1 microgram/ml.
T38514 PMEDAP Others , HIV Protease
PMEDAP is a potent inhibitor of Moloney murine sarcoma virus (MSV)-induced tumor formation and associated mortality and an inhibitor of human immunodeficiency virus (HIV) replication. PMEDAP also has anti-murine cytomega...
T11669 IR415 HBV
IR415 selectively interacts with Hepatitis B virus X protein (HBx, Kd = 2 nM) and blocks HBV-mediated RNAi suppression, reverses the inhibitory effect of HBx protein on the activity of the dicer endoribonuclease. IR415 i...
T38237 2′-O-Methylcytidine Nucleoside Antimetabolite/Analog , HCV Protease
2'-O-Methylcytidine is a nucleoside derivative and an inhibitor of hepatitis C virus (HCV) non-structural protein 5B (NS5B; IC50= 3.8 μM).1It inhibits HCV replication in a replicon assay (IC50= 21.2 μM). 1.Migliaccio, G....
T11539 HCV-IN-29 HCV Protease
HCV-IN-29 is a hepatitis C virus (HCV) inhibitor.
T11541 HCV-IN-30 Others , HCV Protease
HCV-IN-30 is an HCV NS5A replication complex inhibitor (IC50s: 901 and 102 nM for genotypes 1a and 1b replicons).
T9212 IMB-301 Others , HIV Protease
IMB-301 is a small molecular inhibitor via virtual screening according to the hA3G model.
T8354 Triazavirin Nucleoside Antimetabolite/Analog , Influenza Virus , DNA/RNA Synthesis
Triazavirin is a nucleoside analogue of nucleic acid and an antiviral agent.
T11538 Hck-IN-1 HIV Protease , Src , Hck
Hck-IN-1 is a selective Nef-dependent Hck inhibitor (IC50s: 2.8 μM and >20 μM for Nef:Hck complex and Hck) with antiretroviral activity. Hck-IN-1 is a direct and wide HIV-1 Nef antagonist with an IC50 of 100-300 nM for w...
T8371 ML188 Virus Protease , SARS-CoV
ML188 is a selective noncovalent SARS-CoV 3CLpro inhibitor(IC50 : 1.5 μM), with moderate MW and good enzyme and antiviral inhibitory activity.
T11281L FGI-106 tetrahydrochloride Virus Protease , HCV Protease , Influenza Virus , HIV Protease
FGI-106 tetrahydrochloride demonstrates potent inhibitory activity across a broad spectrum of viruses, including those causing hemorrhagic fevers such as Ebola, Rift Valley, and Dengue Fever, with half-maximal effective ...
T7330 Nucleozin Influenza Virus
Nucleozin targets influenza A nucleoprotein (NP), a multifunctional, RNA-binding protein necessary for virus replication.
T14968 Cinanserin hydrochloride SQ 10643 Influenza Virus , 5-HT Receptor
Cinanserin hydrochloride (SQ 10643) is a high affinity antagonist of the 5-HT2 receptor (Ki: 41 nM) and a 3C-like protease inhibitor of severe acute respiratory syndrome coronavirus.
T9716 Ensitrelvir S-217622 SARS-CoV
Ensitrelvir (S-217622) is an orally active inhibitor of SARS-CoV-2 3CL protease with IC50 of 13 nM.
T14495 Baloxavir Baloxavir acid,S-033447 Influenza Virus
Baloxavir (S-033447) is a first-in-class cap-dependent endonuclease inhibitor of the influenza virus polymerase PA subunit.
T0220 Foscarnet sodium Phosphonoformate Virus Protease , Reverse Transcriptase , DNA/RNA Synthesis
Foscarnet sodium (Phosphonoformate) is an antiviral agent used in the treatment of cytomegalovirus retinitis. Foscarnet also shows activity against human herpesviruses and HIV.
T9350 IMP-1088 Others , DNA/RNA Synthesis
IMP-1088 is a potent inhibitor of human N-myristoyltransferases NMT1 and NMT2 dual.
T5429 Theaflavin 3,3'-digallate 8-Gingerol,TFDG Virus Protease , Antioxidant , HIV Protease , HSV
Theaflavin 3,3'-digallate (8-Gingerol) , a major polyphenol found in black tea, is an inducer of oxidative stress which has anti-inflammatory and cancer chemopreventive actions, it reduces tumor angiogenesis by downregul...
T6439 Cetylpyridinium Chloride Cetamium,Pristacin,Hexadecylpyridinium Chloride Others , HBV , Antibacterial
Cetylpyridinium Chloride (Hexadecylpyridinium Chloride) is a cationic quaternary ammonium compound used as oropharyngeal antiseptic.
T1623 Lopinavir ABT-378 SARS-CoV , HIV Protease
Lopinavir (ABT-378) is a peptidomimetic HIV protease inhibitor that retains activity against HIV protease with the Val 82 mutation. Lopinavir is less affected by binding to serum proteins than the structurally-related dr...
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