4.7 Article Proceedings Paper

Anti-HIV drugs: 25 compounds approved within 25 years after the discovery of HIV

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ELSEVIER SCIENCE BV
DOI: 10.1016/j.ijantimicag.2008.10.010

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AIDS; HIV; Nucleoside reverse transcriptase inhibitors (NRTIs); Nucleotide reverse transcriptase inhibitors (NtRTIs); Non-nucleoside reverse transcriptase inhibitors (NNRTIs); Protease inhibitors; Fusion inhibitors; Co-receptor inhibitors; Integrase inhibitors

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In 2008, 25 years after the human immunode efficiency virus (HIV) was discovered as the then tentative aetiological agent of acquired immune deficiency syndrome (AIDS), exactly 25 anti-HIV compounds have been formally approved for clinical use in the treatment of AIDS. These compounds fall into six categories: nucleoside reverse transcriptase inhibitors (NRTIs: zidovudine, didanosine, zalcitabine, stavudine, lamivudine, abacavir and emtricitabine); nucleotide reverse transcriptase inhibitors (NtRTIs: tenofovir); non-nucleoside reverse transcriptase inhibitors (NNRTIs: nevirapine, delavirdine, efavirenz and etravirine); protease inhibitors (PIs: saquinavir, ritonavir, indinavir, nelfinavir, amprenavir, lopinavir, atazanavir, fosamprenavir, tipranavir and darunavir); cell entry inhibitors [fusion inhibitors (FIs: enfuvirtide) and co-receptor inhibitors (CRIs: maraviroc)]; and integrase inhibitors (INIs: raltegravir). These compounds should be used in drug combination regimens to achieve the highest possible benefit, tolerability and compliance and to diminish the risk of resistance development. (c) 2008 Elsevier B.V. and the International Society of Chemotherapy. All rights reserved.

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