[Recent development of novel reverse transcriptase inhibitors and protease inhibitors against HIV-1 infection]. 2010

Yasuhiro Koh
Department of Hematology, Kumamoto University Graduate School of Medical and Pharmaceutical Sciences.

Currently available combinational therapies based on the use of reverse transcriptase inhibitors (RTIs), protease inhibitors (PIs) and other new class drugs such as CCR5 inhibitors and integrase inhibitors for HIV-1 infection and AIDS have been shown to suppress virus replication and extend the life expectancy of HIV-1-infected individuals. Despite this undeniable success, there are limitations associated with current treatment regimens including emergence of drug resistance, complicated dosing protocols, adverse side effects, and increasing cost. Consequently, the development of new RTIs and PIs, including new class drugs, remains essential to the future management of HIV/AIDS. In this paper, the current status of drug development of novel RTIs and PIs is briefly reviewed.

UI MeSH Term Description Entries
D011480 Protease Inhibitors Compounds which inhibit or antagonize biosynthesis or actions of proteases (ENDOPEPTIDASES). Antiprotease,Endopeptidase Inhibitor,Endopeptidase Inhibitors,Peptidase Inhibitor,Peptidase Inhibitors,Peptide Hydrolase Inhibitor,Peptide Hydrolase Inhibitors,Peptide Peptidohydrolase Inhibitor,Peptide Peptidohydrolase Inhibitors,Protease Antagonist,Protease Antagonists,Antiproteases,Protease Inhibitor,Antagonist, Protease,Antagonists, Protease,Hydrolase Inhibitor, Peptide,Hydrolase Inhibitors, Peptide,Inhibitor, Endopeptidase,Inhibitor, Peptidase,Inhibitor, Peptide Hydrolase,Inhibitor, Peptide Peptidohydrolase,Inhibitor, Protease,Inhibitors, Endopeptidase,Inhibitors, Peptidase,Inhibitors, Peptide Hydrolase,Inhibitors, Peptide Peptidohydrolase,Inhibitors, Protease,Peptidohydrolase Inhibitor, Peptide,Peptidohydrolase Inhibitors, Peptide
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D015497 HIV-1 The type species of LENTIVIRUS and the etiologic agent of AIDS. It is characterized by its cytopathic effect and affinity for the T4-lymphocyte. Human immunodeficiency virus 1,HIV-I,Human Immunodeficiency Virus Type 1,Immunodeficiency Virus Type 1, Human
D015658 HIV Infections Includes the spectrum of human immunodeficiency virus infections that range from asymptomatic seropositivity, thru AIDS-related complex (ARC), to acquired immunodeficiency syndrome (AIDS). HTLV-III Infections,HTLV-III-LAV Infections,T-Lymphotropic Virus Type III Infections, Human,HIV Coinfection,Coinfection, HIV,Coinfections, HIV,HIV Coinfections,HIV Infection,HTLV III Infections,HTLV III LAV Infections,HTLV-III Infection,HTLV-III-LAV Infection,Infection, HIV,Infection, HTLV-III,Infection, HTLV-III-LAV,Infections, HIV,Infections, HTLV-III,Infections, HTLV-III-LAV,T Lymphotropic Virus Type III Infections, Human
D018894 Reverse Transcriptase Inhibitors Inhibitors of reverse transcriptase (RNA-DIRECTED DNA POLYMERASE), an enzyme that synthesizes DNA on an RNA template. Reverse Transcriptase Inhibitor,Inhibitors, Reverse Transcriptase,Inhibitor, Reverse Transcriptase,Transcriptase Inhibitor, Reverse

Related Publications

Yasuhiro Koh
June 2008, Virus research,
Yasuhiro Koh
October 2020, Current opinion in pharmacology,
Yasuhiro Koh
June 2018, Expert opinion on emerging drugs,
Yasuhiro Koh
June 2007, Applied microbiology and biotechnology,
Yasuhiro Koh
January 2018, The Journal of antimicrobial chemotherapy,
Yasuhiro Koh
September 1991, Nihon rinsho. Japanese journal of clinical medicine,
Yasuhiro Koh
January 2021, Bioorganic & medicinal chemistry letters,
Yasuhiro Koh
January 2008, Advances in pharmacology (San Diego, Calif.),
Yasuhiro Koh
January 2000, Advances in pharmacology (San Diego, Calif.),
Copied contents to your clipboard!