Antibiotics: Natural Products Essential to Human Health

被引:133
作者
Demain, Arnold L. [1 ]
机构
[1] Drew Univ, RISE, Madison, NJ 07940 USA
关键词
natural products; antibiotics; resistance development; beta-lactams; tetracyclines; macrolides; glycopeptides; lipopeptides; RESISTANT ENTEROCOCCUS-FAECIUM; DRUG DISCOVERY; CHEMICAL DIVERSITY; VANCOMYCIN DERIVATIVES; ANTIBACTERIAL ACTIVITY; MACROLIDE ANTIBIOTICS; STRUCTURE ELUCIDATION; BACTERIAL PATHOGENS; INFECTIOUS-DISEASES; HIGHLY POTENT;
D O I
10.1002/med.20154
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
For more than 50 years, natural products have served us well in combating infectious bacteria and fungi. Microbial and plant secondary metabolites helped to double our life span during the 20th century, reduced pain and Suffering, and revolutionized medicine. Most antibiotics are either (i) natural products of microorganisms, (ii) semi-synthetically produced from natural products, or (iii) chemically synthesized based oil the Structure of the natural products. Production of antibiotics began with penicillin in the late 1940s and proceeded with great success until the 1970-1980s when it became harder and harder to discover new and useful products. Furthermore, resistance development in pathogens became a major problem, Which is still with Lis today. In addition, new pathogens are continually emerging and there are still bacteria that are not eliminated by any antibiotic, e.g., Pseudomonas aeruginosa. In addition to these problems, many of the major pharmaceutical companies have abandoned the antibiotic field, leaving much of the discovery efforts to small companies, new companies, and the biotechnology industries. Despite these problems, development of new antibiotics has continued, albeit Lit a much lower pace than in the last century. We have seen the (i) appearance of newly discovered antibiotics (e.g., candins), (ii) development of old but unutilized antibiotics (e.g., daptomycin), (iii) production of new semi-synthetic versions of old antibiotics (e.g., glycylcyclines, streptogrammins), as well as the (iv) very useful application of old but underutilized antibiotics (e.g., teicoplanin). (C) 2009 Wiley Periodicals, Inc. Med Res Rev, 29, No. 6. 821-842, 2009
引用
收藏
页码:821 / 842
页数:22
相关论文
共 164 条
[1]   Synthesis and antibacterial activity of ketolides (6-O-methyl-3-oxoerythromycin derivatives):: A new class of antibacterials highly potent against macrolide-resistant and -susceptible respiratory pathogens [J].
Agouridas, C ;
Denis, A ;
Auger, JM ;
Benedetti, Y ;
Bonnefoy, A ;
Bretin, F ;
Chantot, JF ;
Dussarat, A ;
Fromentin, C ;
D'Ambrières, SG ;
Lachaud, S ;
Laurin, P ;
Le Martret, O ;
Loyau, V ;
Tessot, N .
JOURNAL OF MEDICINAL CHEMISTRY, 1998, 41 (21) :4080-4100
[2]   Antifungal resistance trends towards the year 2000 - Implications for therapy and new approaches [J].
Alexander, BD ;
Perfect, JR .
DRUGS, 1997, 54 (05) :657-678
[3]  
*AM AC MICR COLL, 2004, MICR 21 CENT AR WE A
[4]  
Andermann A. A. J., 1996, MCJILL J MED, P115
[5]  
[Anonymous], 2008, Molecules that changed the world
[6]  
[Anonymous], 2001, DICT NATURAL PRODUCT
[7]  
Balaban N, 2005, SCIENTIST, V19, P42
[8]   Natural products to drugs: daptomycin and related lipopeptide antibiotics [J].
Baltz, RH ;
Miao, V ;
Wrigley, SK .
NATURAL PRODUCT REPORTS, 2005, 22 (06) :717-741
[9]  
Barriere JC, 1998, CURR PHARM DESIGN, V4, P155
[10]   The millennium bugs - the need for and development of new antibacterials [J].
Bax, R ;
Mullan, N ;
Verhoef, J .
INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2000, 16 (01) :51-59