Table 4.
Name | HIV-1 Inhibition Target | Inhibition Activity | Reference |
---|---|---|---|
Caffeic acid | IN assay in infected MT-2 cells | IC50 inhibition: >278 µM | [149] |
Syncytia formation in Molt-3 cells | 93% inhibtion at 255 µM | [150] | |
Matrix protein by immunofluorescence analysis | 50% inhibtion at 255 µM | [150] | |
Capsid protein by immunofluorescence analysis | 57% inhibtion at 255 µM | [150] | |
RT assay | 32% inhibtion at 255 µM | [150] | |
Ferulic acid | No inhibitory effect | N/A | [151,152] |
Chlorogenic acid | IN assay in infected MT-2 cells | IC50 inhibition: >142 µM | [149] |
RT by colorimetric enzyme immunoassay | IC50 inhibition: 374 µM | [153] | |
Apigenin | RT by PCR assay | IC50: >37.03 µM | [69] |
HIV-1 in infected OM-10.1 cells | IC50 inhibition: 12 µM | [148] | |
Kaempferol | IN integration | IC50 inhibition: 64.7 ± 18.1 µM | [146] |
IN cleavage | IC50 inhibition: 97.8 ± 9.2 µM | [146] | |
RT by PCR assay | IC50 inhibition: >34.94 µM | [69] | |
PR by fluorescence assay | 62.7% inhibition at 174.7 µM | [154] | |
Quercetin | RT by ELOSA | IC50 inhibition: 60 µM | [135] |
PR by oligopeptide cleavage assay | IC50 inhibition: >100 µM | [135] | |
α-glucosidase inhibition assay | IC50 inhibition: >100 µM | [135] | |
IN integration | IC50 inhibition: 13.6 ± 3.4 µM | [146] | |
IN cleavage | IC50 inhibition: 23.6 ± 6.6 µM | [146] | |
RT by PCR assay | IC50 inhibition: <1.65 µM | [69] | |
RT by PCR assay | 100% inhibition at 6.62 µM | [69] | |
RT by ELISA colorimetric enzyme immunoassay | 43.41 ± 4.56% inhibition at 661.7 µM | [155] | |
Isorhamnetin | HIV-1 replication in H9 lymphocyte cells | EC50 inhibition: 6.6 µM | [154] |
RT by ELISA colorimetric enzyme immunoassay | 56.99 ± 3.91% inhibition at 632.4 µM | [155] | |
Myricetin | IN integration | IC50 inhibition: 2.5 ± 1.0 µM | [146] |
IN cleavage | IC50 inhibition: 7.6 ± 0.6 µM | [146] | |
RT by PCR assay | IC50 inhibition: <1.57 µM | [69] | |
RT by PCR assay | 100% inhibition at 6.29 µM | [69] | |
HIV-1 Blood and lymphocytes infected TZM-bl cells | 87% inhibition at 100 µM | [147] | |
HIV-1 Blood and lymphocytes infected TZM-bl cells | IC50 inhibition: 20.43 µM | [147] | |
HIV-1 in infected MT4 cells | EC50 inhibition: 230 µM | [156] | |
RT assay | IC50 inhibition: 7.6 µM | [156] | |
RT | Docking energy: −7.0 kcal/mol | [156] | |
Isoquercitrin | PR by fluorescence assay | 64.4% inhibition at 107.7 µM | [154] |
Myricitrin | PR by fluorescence assay | 50.4% inhibition at 107.7 µM | [154] |
HIV-1 in infected MT4 cells | EC50 inhibition: 120 µM | [156] | |
RT assay | IC50 inhibition: 10.6 µM | [156] | |
RT | Docking energy: −5.0 kcal/mol | [156] |
IC50: Half maximal inhibitory concentration, EC50: Half maximal effective concentration, IN: Integrase, RT: Reverse transcriptase, ELOSA: Enzyme-Linked Oligonucleotide Sorbent Assay, PCR: Polymerase Chain Reaction, ELISA: Enzyme-Linked Immunosorbent Assay, PR: Protease.