Potent and highly selective human immunodeficiency virus type 1 (HIV-1) inhibition by a series of alpha-anilinophenylacetamide derivatives targeted at HIV-1 reverse transcriptase.

Ítems similars

• New tetrahydroimidazo[4,5,1-jk][1,4]-benzodiazepin-2(1H)-one and -thione derivatives are potent inhibitors of human immunodeficiency virus type 1 replication and are synergistic with 2',3'-dideoxynucleoside analogs.
  per: Pauwels, R, et al.
  Publicat: (1994)
• An antiviral target on reverse transcriptase of human immunodeficiency virus type 1 revealed by tetrahydroimidazo-[4,5,1-jk] [1,4]benzodiazepin-2 (1H)-one and -thione derivatives.
  per: Debyser, Z, et al.
  Publicat: (1991)
• Potent and selective inhibition of human immunodeficiency virus (HIV)-1 and HIV-2 replication by a class of bicyclams interacting with a viral uncoating event.
  per: De Clercq, E, et al.
  Publicat: (1992)
• Highly potent and selective inhibition of human immunodeficiency virus by the bicyclam derivative JM3100.
  per: De Clercq, E, et al.
  Publicat: (1994)
• Potent and selective inhibition of human immunodeficiency virus type 1 (HIV-1) by 5-ethyl-6-phenylthiouracil derivatives through their interaction with the HIV-1 reverse transcriptase.
  per: Baba, M, et al.
  Publicat: (1991)