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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T1883 | Des(benzylpyridyl) Atazanavi | HIV Protease | |
The N-dealkylated metabolite (M1) of Atazanavir, a HIV protease inhibitor. | |||
T15210 | Elsulfavirine | Elpida,VM-1500 | HIV Protease |
Elsulfavirine (VM-1500) is an HIV-1 infection reverse transcriptase inhibitor. It is a new anti-HIV drug. | |||
T3523 | Fostemsavir | BMS-663068 | HIV Protease |
Fostemsavir (BMS-663068) is an HIV-1 attachment inhibitor in development for the treatment of HIV-1 infection. | |||
T10570 | Fostemsavir Tris | BMS-663068 Tris | HIV Protease |
Fostemsavir Tris (BMS-663068 Tris) is the prodrug of BMS-626529,is a oral, safe and effective inhibitor of HIV-1 attachment. It inhibits human immunodeficiency virus type 1 (HIV-1) infection by binding to gp120 and inter... | |||
T28255 | Opaviraline | GW420867X,GW-867,HBY-1293,GW867,GW-420867X | HIV Protease |
Opaviraline (GW-420867X) is a potent reverse transcriptase inhibitor that inhibits Human immunodeficiency virus 1 and has the potential to treat HIV infection. | |||
T67804 | KM-023 | HIV Protease | |
KM-023 is a new second-generation non-nucleoside reverse transcriptase inhibitor for the study of human immunodeficiency virus (HIV) type 1 infection. | |||
T27625 | IQP-0528 | SJ-3991,SJ3991,IQP0528 | Antiviral , HIV Protease , Reverse Transcriptase |
IQP-0528 is a potent non-nucleoside reverse transcriptase inhibitor (NNRTI) that has potential for the treatment of HIV infection by blocking viral entry and shows antiviral activity as a microbicidal gel. . IQP-0528 sho... | |||
T15371 | Gardiquimod | TLR , HIV Protease | |
Gardiquimod is a TLR7/8 agonist. When used at concentrations below 10 μM, Gardiquimod specifically activates TLR7. Gardiquimod could inhibit HIV-1 infection of macrophages and activated peripheral blood mononuclear cells... | |||
T11074 | Dolutegravir intermediate-1 | 1-(2,2-dimethoxyethyl)-5-methoxy-6-methoxycarbonyl-4-oxopyridine-3-carboxylic acid,1-(2,2-dimethoxyethyl)-5-methoxy-6-(methoxycarbonyl)-4-oxo-1,4-dihydropyridine-3-carboxylic acid | HIV Protease |
Dolutegravir intermediate-1 (1-(2,2-dimethoxyethyl)-5-methoxy-6-(methoxycarbonyl)-4-oxo-1,4-dihydropyridine-3-carboxylic acid) is a new synthetic Dolutegravir intermediate. Dolutegravir is an integrase inhibitor develope... | |||
TN5263 | 1-[2,4-Dihydroxy-6-methoxy-3-(3-methyl-2-buten-1-yl)phenyl]-3-(4-hydroxyphenyl)-2-propen-1-one | Xanthohumol | Apoptosis , BCL , PARP , HCV Protease , IAP , Caspase , HIV Protease , NMDAR , p53 |
1-[2,4-Dihydroxy-6-methoxy-3-(3-methyl-2-buten-1-yl)phenyl]-3-(4-hydroxyphenyl)-2-propen-1-one (Xanthohumol) , prenylchacone flavonoid, is a natural product with multi-biofunctions purified from Hops Humulus lupulus,is e... | |||
T27154 | Dexelvucitabine | D-D-4FC,DPC-817,RVT,beta-D-D-4FC,DFC | Reverse Transcriptase |
Dexelvucitabine (RVT), a nucleoside reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection. | |||
T16500 | PF-3450074 | PF-74 | HIV Protease |
PF-3450074 (PF-74) acts at an early stage of HIV-1 infection inhibits viral replication by directly competing with the binding of CPSF6 (nuclear host factors cleavage and polyadenylation specific factor 6) and NUP153 (nu... | |||
T26240 | Surfen dihydrochloride | Aminokinuride dihydrochloride,Aminoquinuride dihydrochloride,NSC-12155,Aminokinuride 2HCl,Aminoquinuride 2HCl | FGFR , Antiviral , Antibiotic |
Surfen dihydrochloride (Aminoquinuride dihydrochloride) is a potent small molecule antagonist of heparin sulfate with antibacterial and antiviral activity, and inhibits anthrax lethal factor, coagulation factor X, and le... | |||
T11564 | HIV-1 inhibitor-3 | Others | |
HIV-1 inhibitor-3 is an HIV infection inhibitor. | |||
T15483 | LEDGIN6 | HIV-1 integrase inhibitor 2 | Others |
HIV-1 integrase inhibitor 2 is used for the treatment of human immunodeficiency virus (HIV) infection. | |||
T76537 | GP120, HIV-1 MN | ||
GP120, HIV-1 MN, a peptide, is utilized in researching HIV infection [1] [2]. | |||
T27742 | KRH-3955 Salt | KRH-3955,KRH3955,KRH 3955,KRH3955 Salt | |
KRH-3955, a CXCR4 antagonist, is an orally bioavailable and extremely potent inhibitor of HIV-1 infection. | |||
T28171 | Nifeviroc | TD-0232,TD 0232,TD0232 | |
Nifeviroc, a CCR5 antagonist, is used potentially for treatment of inflammatory responses to HIV type-1 infection. | |||
T28492 | R-18893 | R18893 | |
R-18893, a RNA-directed DNA polymerase inhibitor, is used potentially for the treatment of HIV-1 infection. | |||
T71056 | SJP-L-5 | ||
SJP-L-5 is a inhibitor of HIV-1 infection by blocking viral DNA nuclear entry. |