1,4-benzodiazepin-2-ones in medicinal chemistry

被引:41
作者
Spencer, John [1 ]
Rathnam, Rajendra P. [1 ]
Chowdhry, Babur Z. [1 ]
机构
[1] Univ Greenwich Medway, Sch Sci, Chatham ME4 4TB, Kent, England
关键词
RECEPTOR ANTAGONISTS; COMBINATORIAL SYNTHESIS; BIOLOGICAL EVALUATION; PRIVILEGED STRUCTURES; CCK2; ANTAGONISTS; HIGHLY POTENT; BENZODIAZEPINE; INHIBITORS; DERIVATIVES; NONPEPTIDE;
D O I
10.4155/FMC.10.226
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
1,4-benzodiazepin-2-ones have applications in many areas of medicinal chemistry that are not restricted to 'classical' CNS treatments such as sedatives, epilepsy and muscle relaxants. We will describe selected examples of 1,4-benzodiazepin-2-ones in other areas of medicinal chemistry including uses as G-protein-coupled receptor antagonists, enzyme inhibitors and anticancer agents. Examples from our group will mainly show the use of palladacycle complexes of 1,4-benzodiazepin-2-ones as anticancer agents.
引用
收藏
页码:1441 / 1449
页数:9
相关论文
共 71 条
  • [61] BENZODIAZEPINE STORY
    STERNBACH, LH
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1979, 22 (01) : 1 - 7
  • [62] Stokes T., 2004, CLIN GUIDELINES EVID
  • [63] Stuart DR, 2007, SCIENCE, V316, P1172, DOI 10.1126/science.1141956
  • [64] The immunomodulatory benzodiazepine Bz-423 inhibits B-cell proliferation by targeting c-Myc protein for rapid and specific degradation
    Sundberg, TB
    Ney, GM
    Subramanian, C
    Opipari, AW
    Glick, GD
    [J]. CANCER RESEARCH, 2006, 66 (03) : 1775 - 1782
  • [65] Taylor D., 1987, The Benzodiazepines in Current Clinical Practice, P13
  • [66] Ring forming reactions of imines of 2-aminobenzaldehyde and related compounds
    Wiklund, P
    Bergman, J
    [J]. ORGANIC & BIOMOLECULAR CHEMISTRY, 2003, 1 (02) : 367 - 372
  • [67] Non-peptide calcitonin gene-related peptide receptor antagonists from a benzodiazepinone lead
    Williams, TM
    Stump, CA
    Nguyen, DN
    Quigley, AG
    Bell, IM
    Gallicchio, SN
    Zartman, CB
    Wan, BL
    Della Penna, K
    Kunapuli, P
    Kane, SA
    Koblan, KS
    Mosser, SD
    Rutledge, RZ
    Salvatore, C
    Fay, JF
    Vacca, JP
    Graham, SL
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2006, 16 (10) : 2595 - 2598
  • [68] Benzodiazepines as potent and selective bradykinin B1 antagonists
    Wood, MR
    Kim, JJ
    Han, W
    Dorsey, BD
    Homnick, CF
    DiPardo, RM
    Kuduk, SD
    MacNeil, T
    Murphy, KL
    Lis, EV
    Ransom, RW
    Stump, GL
    Lynch, JJ
    O'Malley, SS
    Miller, PJ
    Chen, TB
    Harrell, CM
    Chang, RSL
    Sandhu, P
    Ellis, JD
    Bondiskey, PJ
    Pettibone, DJ
    Freidinger, RM
    Bock, MG
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 2003, 46 (10) : 1803 - 1806
  • [69] A highly practical route to 7-hydroxy-1,3-dihydro-2H-1,4-benzodiazepin-2-one from p-anisidine
    Wu, CD
    Biediger, RJ
    Kogan, TP
    [J]. SYNTHETIC COMMUNICATIONS, 1999, 29 (20) : 3509 - 3516
  • [70] Application of Daugulis Copper-Catalyzed Direct Arylation to the Synthesis of 5-Aryl Benzotriazepines
    Yotphan, Sirilata
    Bergman, Robert G.
    Ellman, Jonathan A.
    [J]. ORGANIC LETTERS, 2009, 11 (07) : 1511 - 1514