New developments in anti-HIV chemotherapy

Curr Med Chem. 2001 Nov;8(13):1543-72. doi: 10.2174/0929867013371842.


Virtually all the compounds that are currently used, or under advanced clinical trial, for the treatment of HIV infections, belong to one of the following classes: (i) nucleoside/nucleotide reverse transcriptase inhibitors (NRTIs): i.e., zidovudine (AZT), didanosine (ddI), zalcitabine (ddC), stavudine (d4T), lamivudine (3TC), abacavir (ABC), emtricitabine [(-)FTC], tenofovir (PMPA) disoproxil fumarate; (ii) non-nucleoside reverse transcriptase inhibitors (NNRTIs): i.e., nevirapine, delavirdine, efavirenz, emivirine (MKC-442); and (iii) protease inhibitors (PIs): i.e., saquinavir, ritonavir, indinavir, nelfinavir, amprenavir, and lopinavir. In addition to the reverse transcriptase and protease step, various other events in the HIV replicative cycle are potential targets for chemotherapeutic intervention: (i) viral adsorption, through binding to the viral envelope glycoprotein gp120 (polysulfates, polysulfonates, polyoxometalates, zintevir, negatively charged albumins, cosalane analogues); (ii) viral entry, through blockade of the viral coreceptors CXCR4 and CCR5 [bicyclams (i.e. AMD3100), polyphemusins (T22), TAK-779, MIP-1 alpha LD78 beta isoform]; (iii) virus-cell fusion, through binding to the viral glycoprotein gp41 [T-20 (DP-178), T-1249 (DP-107), siamycins, betulinic acid derivatives]; (iv) viral assembly and disassembly, through NCp7 zinc finger-targeted agents [2,2'-dithiobisbenzamides (DIBAs), azadicarbonamide (ADA) and NCp7 peptide mimics]; (v) proviral DNA integration, through integrase inhibitors such as L-chicoric acid and diketo acids (i.e. L-731,988); (vi) viral mRNA transcription, through inhibitors of the transcription (transactivation) process (fluoroquinolone K-12, Streptomyces product EM2487, temacrazine, CGP64222). Also, in recent years new NRTIs, NNRTIs and PIs have been developed that possess respectively improved metabolic characteristics (i.e. phosphoramidate and cyclosaligenyl pronucleotides of d4T), or increased activity against NNRTI-resistant HIV strains [second generation NNRTIs, such as capravirine and the novel quinoxaline, quinazolinone, phenylethylthiazolylthiourea (PETT) and emivirine (MKC-442) analogues], or, as in the case of PIs, a different, non-peptidic scaffold [i.e. cyclic urea (DMP 450), 4-hydroxy-2-pyrone (tipranavir)]. Given the multitude of molecular targets with which anti-HIV agents can interact, one should be cautious in extrapolating from cell-free enzymatic assays to the mode of action of these agents in intact cells. A number of compounds (i.e. zintevir and L-chicoric acid, on the one hand; and CGP64222 on the other hand) have recently been found to interact with virus-cell binding and viral entry in contrast to their proposed modes of action targeted at the integrase and transactivation process, respectively.

Publication types

  • Review

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Anti-HIV Agents / chemistry*
  • Anti-HIV Agents / pharmacology*
  • Binding Sites
  • Capsid / drug effects
  • Capsid Proteins*
  • Drug Design*
  • Enfuvirtide
  • Enzyme Inhibitors / pharmacology
  • Gene Products, gag / drug effects
  • HIV / drug effects
  • HIV / physiology
  • HIV Envelope Protein gp41 / chemistry
  • HIV Envelope Protein gp41 / drug effects
  • HIV Envelope Protein gp41 / metabolism
  • HIV Envelope Protein gp41 / pharmacology
  • HIV Integrase / drug effects
  • HIV Reverse Transcriptase / drug effects
  • HIV Reverse Transcriptase / metabolism
  • Humans
  • Molecular Sequence Data
  • Peptide Fragments / chemistry
  • Peptide Fragments / pharmacology
  • Reverse Transcriptase Inhibitors / pharmacology
  • Transcription, Genetic / drug effects
  • Viral Proteins*
  • gag Gene Products, Human Immunodeficiency Virus


  • Anti-HIV Agents
  • Capsid Proteins
  • Enzyme Inhibitors
  • Gene Products, gag
  • HIV Envelope Protein gp41
  • NCP7 protein, Human immunodeficiency virus 1
  • Peptide Fragments
  • Reverse Transcriptase Inhibitors
  • Viral Proteins
  • gag Gene Products, Human Immunodeficiency Virus
  • Enfuvirtide
  • HIV Integrase
  • HIV Reverse Transcriptase