How were new medicines discovered?

被引:1277
作者
Swinney, David C. [1 ,2 ]
Anthony, Jason [1 ]
机构
[1] Roche Palo Alto, Palo Alto, CA 94304 USA
[2] IRND3, Inst Rare & Neglected Dis Drug Discovery, Belmont, CA 94002 USA
关键词
DOPAMINE AUTORECEPTOR AGONIST; ESTROGEN-RECEPTOR-ALPHA; GROWTH-FACTOR; (4-HYDROXYPHENYL)PYRUVATE DIOXYGENASE; BIOCHEMICAL-MECHANISMS; FUNCTIONAL SELECTIVITY; PROGESTERONE-RECEPTOR; ENVELOPED VIRUSES; PANCREATIC LIPASE; STRAND TRANSFER;
D O I
10.1038/nrd3480
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Preclinical strategies that are used to identify potential drug candidates include target-based screening, phenotypic screening, modification of natural substances and biologic-based approaches. To investigate whether some strategies have been more successful than others in the discovery of new drugs, we analysed the discovery strategies and the molecular mechanism of action (MMOA) for new molecular entities and new biologics that were approved by the US Food and Drug Administration between 1999 and 2008. Out of the 259 agents that were approved, 75 were first-in-class drugs with new MMOAs, and out of these, 50 (67%) were small molecules and 25 (33%) were biologics. The results also show that the contribution of phenotypic screening to the discovery of first-in-class small-molecule drugs exceeded that of target-based approaches-with 28 and 17 of these drugs coming from the two approaches, respectively-in an era in which the major focus was on target-based approaches. We postulate that a target-centric approach for first-in-class drugs, without consideration of an optimal MMOA, may contribute to the current high attrition rates and low productivity in pharmaceutical research and development.
引用
收藏
页码:507 / 519
页数:13
相关论文
共 162 条
[1]  
Alvaro G, 2007, CURR OPIN DRUG DISC, V10, P613
[2]   Biochemical characterization of desloratadine, a potent antagonist of the human histamine H1 receptor [J].
Anthes, JC ;
Gilchrest, H ;
Richard, C ;
Eckel, S ;
Hesk, D ;
West, RE ;
Williams, SM ;
Greenfeder, S ;
Billah, M ;
Kreutner, W ;
Egan, RW .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2002, 449 (03) :229-237
[3]   Electrophysiological effects of ranolazine, a novel antianginal agent with antiarrhythmic properties [J].
Antzelevitch, C ;
Belardinelli, L ;
Zygmunt, AC ;
Burashnikov, A ;
Di Diego, JM ;
Fish, JM ;
Cordeiro, JM ;
Thomas, G .
CIRCULATION, 2004, 110 (08) :904-910
[4]   Innovations and challenges in renal cancer: Consensus statement from the first international conference [J].
Atkins, MB ;
Avigan, DE ;
Bukowski, RM ;
Childs, RW ;
Dutcher, JP ;
Eisen, TG ;
Figlin, RA ;
Finke, JH ;
Flanigan, RC ;
George, DJ ;
Goldberg, SN ;
Gordon, MS ;
Iliopoulos, O ;
Kaelin, WG ;
Linehan, WM ;
Lipton, A ;
Motzer, RJ ;
Novick, AC ;
Stadler, WM ;
Teh, BT ;
Yang, JC ;
King, L .
CLINICAL CANCER RESEARCH, 2004, 10 (18) :6277S-6281S
[5]   Studies leading to the identification of ZD1839 (Iressa™):: An orally active, selective epidermal growth factor receptor tyrosine kinase inhibitor targeted to the treatment of cancer [J].
Barker, AJ ;
Gibson, KH ;
Grundy, W ;
Godfrey, AA ;
Barlow, JJ ;
Healy, MP ;
Woodburn, JR ;
Ashton, SE ;
Curry, BJ ;
Scarlett, L ;
Henthorn, L ;
Richards, L .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2001, 11 (14) :1911-1914
[6]   INVITRO ANTIFUNGAL ACTIVITIES AND INVIVO EFFICACIES OF 1,3-BETA-D-GLUCAN SYNTHESIS INHIBITORS L-671,329, L-646,991, TETRAHYDROECHINOCANDIN-B, AND L-687,781, A PAPULACANDIN [J].
BARTIZAL, K ;
ABRUZZO, G ;
TRAINOR, C ;
KRUPA, D ;
NOLLSTADT, K ;
SCHMATZ, D ;
SCHWARTZ, R ;
HAMMOND, M ;
BALKOVEC, J ;
VANMIDDLESWORTH, F .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1992, 36 (08) :1648-1657
[7]   REGIO AND STEREOSPECIFIC SYNTHESIS OF 11-BETA-SUBSTITUTED 19-NORSTEROIDS - INFLUENCE OF 11-BETA-SUBSTITUTION ON PROGESTERONE-RECEPTOR AFFINITY [J].
BELANGER, A ;
PHILIBERT, D ;
TEUTSCH, G .
STEROIDS, 1981, 37 (04) :361-382
[8]   Benefits of targeting both pericytes and endothelial cells in the tumor vasculature with kinase inhibitors [J].
Bergers, G ;
Song, S ;
Meyer-Morse, N ;
Bergsland, E ;
Hanahan, D .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 111 (09) :1287-1295
[9]   The beautiful cell: high-content screening in drug discovery [J].
Bickle, Marc .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2010, 398 (01) :219-226
[10]   The metabolic and molecular bases of tetrahydroblopterin-responsive phenylalanine hydroxylase deficiency [J].
Blau, N ;
Erlandsen, H .
MOLECULAR GENETICS AND METABOLISM, 2004, 82 (02) :101-111