A number of laboratories are actively involved in the development of antiviral agents that interfere with HIV at different stages of viral replication.3 and 4 However, the rapid spread of the AIDS epidemic and the appearance of HIV strains resistant to the currently available drugs suggest that effective and durable chemotherapy of this disease will require the use of innovative combinations of drugs having see more diverse mechanisms of anti-HIV activity.5, 6 and 7 For this reason, there is a continuous need for alternative inhibitors. New chemical entities with such activities may be identified through a variety

of approaches, one of them being screening of natural products. Over the last few years, antiviral researchers have also turned toward many of Pazopanib molecular weight the traditional folk medicine, invariably a ‘cocktail’ of natural products, to uncover the scientific basis of their remedial effects. Ng, Vlietinck and Matthee8, 9 and 10

reviewed plant-derived anti-HIV compounds, which serves to underline the fact that selected medicinal plants with HIV-inhibitory activity are widely distributed in nature.11 and 12 HIV-1 encodes three major enzymes, Protease (PR), Reverse Transcriptase (RT) and Integrase (IN). HIV-1 PR processes viral proteins into functional enzymes and structural proteins. HIV-1 RT is the multifunctional enzyme that transcripts viral RNA to viral DNA which is important for viral replication, whereas integrase is responsible for the integration

of dsDNA transcribed from viral RNA into the host chromosome.13 For HIV-1 PR, many inhibitors have been synthesized chemically and used intensively for AIDS treatments. However, their use is limited due to the emergence of drug resistance and toxicity.14 Thus, screening of natural products provides an opportunity for the discovery of HIV-1 inhibitors with lesser or no toxicity and side effects. There are several steps in HIV virus replication in Dichloromethane dehalogenase which antiretroviral drugs can interfere. The first step is adherence of the virus particle to the CD4 positive cell and consecutive fusion with the cell. The next step is transcription of the virus RNA by reverse transcriptase in a DNA strand, which is built into the DNA of the host cell with the enzyme Integrase. After integration of proviral DNA into the host cell, the cell produces a long protein chain. This protein chain has to be snipped into small protein chains with the enzyme protease. At the end of 1980′s and the beginning of 1990′s, the nucleoside reverse transcriptase (NRTIs) was the only anti-retroviral drugs available. Patients were treated with these drugs as monotherapy. Suboptimal suppression of the HIV virus resulted in resistance.