| S4428 | Tenofovir alafenamide fumarate | Tenofovir alafenamide (TAF, GS-7340) fumarate is a prodrug of tenofovir but results in significantly higher intracellular tenofovir concentrations and lower serum levels. Tenofovir alafenamide is a novel nucleotide reverse transcriptase inhibitor for the treatment of HIV-1 infection. | Selective |  | 
            
                
                    | S5068 | Adefovir | Adefovir is an orally administered nucleotide analog reverse transcriptase inhibitor used for treatment of hepatitis B and herpes simplex virus infection. | Selective |  | 
            
                
                    | S8055 | Lersivirine (UK-453061) | Lersivirine (UK-453061) is a potent and selective inhibitor of nonnucleoside reverse transcriptase (NNRTI) with IC50 of 0.119 μM. | Selective |  | 
            
                
                    | S5959 | Tenofovir Disoproxil | Tenofovir Disoproxil (Bis(POC)-PMPA, GS 4331) is a prodrug of tenofovir, which is metabolised intracellularly to its active anabolite tenofovir diphosphate, a competitive inhibitor of HIV-1 reverse transcriptase and terminates the growing DNA chain. | Selective |  | 
            
                
                    | S4427 | Tenofovir alafenamide hemifumarate | Tenofovir alafenamide (TAF, GS-7340) hemifumarate is a prodrug of tenofovir but results in significantly higher intracellular tenofovir concentrations and lower serum levels. Tenofovir alafenamide is a novel nucleotide reverse transcriptase inhibitor for the treatment of HIV-1 infection. | Selective |  | 
            
                
                    | S4685 | Efavirenz | Efavirenz is a synthetic non-nucleoside reverse transcriptase (RT) inhibitor with antiviral activity. | Selective |  | 
            
                
                    | S5215 | Abacavir (1592U89) | Abacavir (1592U89, ABC) is a powerful nucleoside analog reverse transcriptase inhibitor (NRTI) used to treat HIV and AIDS. | Selective |  | 
            
                
                    | S1702 | Didanosine | Didanosine is a reverse transcriptase inhibitor with an IC50 of 0.49 μM. | Selective | Reverse transcriptase, IC50: 490 nM | 
            
                
                    | S1398 | Stavudine (d4T) | Stavudine (d4T, BMY-27857, Sanilvudine, NSC 163661) is a nucleoside analog reverse transcriptase inhibitor (NARTI) active against HIV. | Selective |  | 
            
                
                    | S3080 | Etravirine | Etravirine is a non-nucleoside reverse transcriptase inhibitor (NNRTI) used for the treatment of HIV. | Selective |  | 
            
                
                    | S1742 | Nevirapine (NSC 641530) | Nevirapine (NSC 641530,NVP) is a non-nucleoside reverse transcriptase inhibitor (NNRTI) used to treat HIV-1 infection and AIDS. | Selective |  | 
            
                
                    | S1401 | Tenofovir | Tenofovir (GS-1278) blocks reverse transcriptase and hepatitis B virus infections. | Selective |  | 
            
                
                    | S7856 | Tenofovir Alafenamide (GS-7340) | Tenofovir Alafenamide (GS-7340) is a prodrug of tenofovir, which is a reverse transcriptase inhibitor, used to treat HIV and Hepatitis B. | Selective |  | 
            
                
                    | S3273 | Hypericin | Hypericin (Hyp, HY) is a naturally occurring substance found in the common St. John's Wort (Hypericum species) with antidepressive, antineoplastic and antiviral (human immunodeficiency and hepatitis C virus) activities. Hypericin has inhibitory effects on MAO (monoaminoxidase), PKC (protein kinase C), dopamine-beta-hydroxylase, reverse transcriptase, telomerase and CYP (cytochrome P450). | Selective |  | 
            
                
                    | S1252 | Entecavir Hydrate | Entecavir Hydrate (ETV, Baraclude,BMS200475 Hydrate,SQ34676 Hydrate), a new deoxyguanine nucleoside analogue, is a selective inhibitor of the replication of the hepatitis B virus (HBV). | Selective |  | 
            
                
                    | S1706 | Lamivudine | Lamivudine is a potent nucleoside analog reverse transcriptase inhibitor, used for treatment of chronic HBV and HIV/AIDS. It works by blocking the HIV reverse transcriptase and hepatitis B virus polymerase. | Selective |  | 
            
                
                    | S2579 | Zidovudine | Zidovudine (ZDV, Azidothymidine, NSC 602670,Retrovir) is a nucleoside analogue reverse transcriptase inhibitor, used to treat HIV. It could decrease the HDR efficiency and decrease CRISPR-mediated sequence-specific genome knockin events while increaseing knockout efficiency. | Selective |  | 
            
                
                    | S7303 | Rilpivirine | Rilpivirine (R278474, TMC27, DB08864) is a non-nucleoside reverse transcriptase inhibitor (NNRTI), and used to treat HIV-1 infection. | Selective |  | 
            
                
                    | S6848 | 3'-Fluoro-3'-deoxythymidine (Alovudine) | 3'-Fluoro-3'-deoxythymidine (Alovudine, CL 184824, FddThd, FLT, MIV-310) is a potent inhibitor of polymerase γ and reverse transcriptase that can be used in the treatment of HIV infection. 3'-Fluoro-3'-deoxythymidine (Alovudine) is also a marker of DNA synthesis that can be used as an early response biomarker in the  chemotherapy of pancreatic cancer. | Selective |  | 
            
                
                    | S4187 | Salicylanilide | Salicylanilides (WR10019,2-Hydroxybenzanilide) are a group of compounds with a wide range of biological activities including antiviral potency, antibacterial (including antimycobacterial) and antifungal activities. | Selective |  | 
            
                
                    | S1704 | Emtricitabine (BW 1592) | Emtricitabine (BW1592, FTC) is a new nucleoside agent that has activity against both human immunodeficiency virus (HIV) and hepatitis B virus. It is a reverse transcriptase inhibitor. Intracellular half-life is 39 h. | Selective |  | 
            
                
                    | S3076 | Foscarnet Sodium | Foscarnet Sodium (Phosphonoformate) inhibits viral RNA polymerases, reverse transcriptase, and DNA polymerases through noncompetitive inhibition with dNTPs. | Selective |  |