In search of a novel anti-HIV drug:: Multidisciplinary coordination in the discovery of 4-[[4-[[4-[(1E)-2-cyanoethenyl]-2,6dimethylphenyl] amino]-2-pyrimidinyl]amino]-benzonitrile (R278474, rilpivirine)

被引:292
作者
Janssen, PAJ
Lewi, PJ [1 ]
Arnold, E
Daeyaert, F
de Jonge, M
Heeres, J
Koymans, L
Vinkers, M
Guillemont, J
Pasquier, E
Kukla, M
Ludovici, D
Andries, K
de Béthune, MP
Pauwels, R
Das, K
Clark, AD
Frenkel, YV
Hughes, SH
Medaer, B
De Knaep, F
Bohets, H
De Clerck, F
Lampo, A
Williams, P
Stoffels, P
机构
[1] Janssen Pharmaceut, B-2350 Vosselaar, Belgium
[2] Rutgers State Univ, Ctr Adv Biotechnol & Med, Piscataway, NJ 08854 USA
[3] Rutgers State Univ, Dept Chem & Chem Biol, Piscataway, NJ 08854 USA
[4] Johnson & Johnson Pharmaceut Res & Dev, Med Chem, Janssen Cilag France, F-27106 Val De Reuil, France
[5] Johnson & Johnson Pharmaceut Res & Dev, Drug Discovery, Spring House, PA 19477 USA
[6] Tibotec, B-2800 Mechelen, Belgium
[7] NCI, Frederick, MD 21702 USA
[8] Johnson & Johnson Pharmaceut Res & Dev, Drug Evaluat, B-2340 Beerse, Belgium
[9] Johnson & Johnson Pharmaceut Res & Dev, Drug Dev, B-2340 Beerse, Belgium
[10] Johnson & Johnson Pharmaceut Res & Dev, Drug Evaluat, High Wycombe HP144GT, Bucks, England
关键词
D O I
10.1021/jm040840e
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Ideally, an anti-HIV drug should (1) be highly active against wild-type and mutant HIV without allowing breakthrough; (2) have high oral bioavailability and long elimination half-life, allowing once-daily oral treatment at low doses; (3) have minimal adverse effects; and (4) be easy to synthesize and formulate. R278474, a new diarylpyrimidine (DAPY) non-nucleoside reverse transcriptase inhibitor (NNRTI), appears to meet these criteria and to be suitable for high compliance oral treatment of HIV-1 infection. The discovery of R278474 was the result of a coordinated multidisciplinary effort involving medicinal chemists, virologists, crystallographers, molecular modelers, toxicologists, analytical chemists, pharmacists, and many others.
引用
收藏
页码:1901 / 1909
页数:9
相关论文
共 59 条
  • [1] ANDRIES K, 2004, IN PRESS AACN CLIN I
  • [2] Bohets Hilde, 2001, Current Topics in Medicinal Chemistry, V1, P367, DOI 10.2174/1568026013394886
  • [3] BOULTON AA, 1986, RECEPTOR BINDING
  • [4] Charman WN., 1992, LYMPHATIC TRANSPORT
  • [5] GUIDE FOR PERFORMING THE MOUSE LYMPHOMA ASSAY FOR MAMMALIAN-CELL MUTAGENICITY
    CLIVE, D
    CASPARY, W
    KIRBY, PE
    KREHL, R
    MOORE, M
    MAYO, J
    OBERLY, TJ
    [J]. MUTATION RESEARCH, 1987, 189 (02): : 143 - 156
  • [6] Coffin J. M., 1997, RETROVIRUSES
  • [7] HIV POPULATION-DYNAMICS IN-VIVO - IMPLICATIONS FOR GENETIC-VARIATION, PATHOGENESIS, AND THERAPY
    COFFIN, JM
    [J]. SCIENCE, 1995, 267 (5197) : 483 - 489
  • [8] Crystal structures of 8-Cl and 9-Cl TIBO complexed with wild-type HIV-1 RT and 8-Cl TIBO complexed with the Tyr181Cys HIV-1 RT drug-resistant mutant
    Das, K
    Ding, JP
    Hsiou, Y
    Clark, AD
    Moereels, H
    Koymans, L
    Andries, K
    Pauwels, R
    Janssen, PAJ
    Boyer, PL
    Clark, P
    Smith, RH
    Smith, MBK
    Michejda, CJ
    Hughes, SH
    Arnold, E
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1996, 264 (05) : 1085 - 1100
  • [9] Roles of conformational and positional adaptability in structure-based design of TMC125-R165335 (etravirine) and related non-nucleoside reverse transcriptase inhibitors that are highly potent and effective against wild-type and drug-resistant HIV-1 variants
    Das, K
    Clark, AD
    Lewi, PJ
    Heeres, J
    de Jonge, MR
    Koymans, LMH
    Vinkers, HM
    Daeyaert, F
    Ludovici, DW
    Kukla, MJ
    De Corte, B
    Kavash, RW
    Ho, CY
    Ye, H
    Lichtenstein, MA
    Andries, K
    Pauwels, R
    de Béthune, MP
    Boyer, PL
    Clark, P
    Hughes, SH
    Janssen, PAJ
    Arnold, E
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 2004, 47 (10) : 2550 - 2560
  • [10] De Clercq E, 2002, MED RES REV, V22, P531