Chiral Alkyl Halides: Underexplored Motifs in Medicine

被引:100
作者
Gal, Balint [1 ]
Bucher, Cyril [1 ]
Burns, Noah Z. [1 ]
机构
[1] Stanford Univ, Dept Chem, 333 Campus Dr, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
alkyl halide; stereochemistry; lipophilicity; anesthetic; clindamycin; corticosteroid; pimecrolimus; sucralose; halomon; lapachone; astins; forazoline; ALGA PORTIERIA-HORNEMANNII; TUMOR-CELL-LINES; BETA-LAPACHONE; NATURAL-PRODUCTS; STRUCTURAL BASIS; DRUG DISCOVERY; HALOGEN BOND; IN-VIVO; BINDING; ANTIBIOTICS;
D O I
10.3390/md14110206
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
While alkyl halides are valuable intermediates in synthetic organic chemistry, their use as bioactive motifs in drug discovery and medicinal chemistry is rare in comparison. This is likely attributable to the common misconception that these compounds are merely non-specific alkylators in biological systems. A number of chlorinated compounds in the pharmaceutical and food industries, as well as a growing number of halogenated marine natural products showing unique bioactivity, illustrate the role that chiral alkyl halides can play in drug discovery. Through a series of case studies, we demonstrate in this review that these motifs can indeed be stable under physiological conditions, and that halogenation can enhance bioactivity through both steric and electronic effects. Our hope is that, by placing such compounds in the minds of the chemical community, they may gain more traction in drug discovery and inspire more synthetic chemists to develop methods for selective halogenation.
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页数:11
相关论文
共 47 条
[1]   Systemic exposure, tolerability, and efficacy of pimecrolimus cream 1% in atopic dermatitis patients [J].
Allen, BR ;
Lakhanpaul, M ;
Morris, A ;
Lateo, S ;
Davies, T ;
Scott, G ;
Cardno, M ;
Ebelin, ME ;
Burtin, P ;
Stephenson, TJ .
ARCHIVES OF DISEASE IN CHILDHOOD, 2003, 88 (11) :969-973
[2]   DNA methyl transferase inhibiting halogenated monoterpenes from the Madagascar red marine alga Portieria hornemannii [J].
Andrianasolo, EH ;
France, D ;
Cornell-Kennon, S ;
Gerwick, WH .
JOURNAL OF NATURAL PRODUCTS, 2006, 69 (04) :576-579
[3]   Therapeutic strategies for allergic diseases [J].
Barnes, PJ .
NATURE, 1999, 402 (6760) :B31-B38
[4]  
Bucher C., 2016, UNPUB
[5]   Highly Selective Synthesis of Halomon, Plocamenone, and Isoplocamenone [J].
Bucher, Cyril ;
Deans, Richard M. ;
Burns, Noah Z. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2015, 137 (40) :12784-12787
[6]   Glucocorticoid receptor binding: A biphasic dependence on molecular size as revealed by the bilinear LinBiExp model [J].
Buchwald, Peter .
STEROIDS, 2008, 73 (02) :193-208
[7]   EVIDENCE FOR BIOGENESIS OF HALOGENATED MYRCENES FROM RED ALGA CHONDROCOCCUS-HORNEMANNI [J].
BURRESON, BJ ;
WOOLARD, FX ;
MOORE, RE .
CHEMISTRY LETTERS, 1975, (11) :1111-1114
[8]   The Halogen Bond [J].
Cavallo, Gabriella ;
Metrangolo, Pierangelo ;
Milani, Roberto ;
Pilati, Tullio ;
Priimagi, Arri ;
Resnati, Giuseppe ;
Terraneo, Giancarlo .
CHEMICAL REVIEWS, 2016, 116 (04) :2478-2601
[9]   Antimalarial activity of phenazines from lapachol, β-lapachone and its derivatives against Plasmodium falciparum in vitro and Plasmodium berghei in vivo [J].
de Andrade-Neto, VF ;
Goulart, MOF ;
da Silva, JF ;
da Silva, MJ ;
Pinto, MD ;
Pinto, AV ;
Zalis, MG ;
Carvalho, LH ;
Krettli, AU .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2004, 14 (05) :1145-1149
[10]   INTERACTION OF THE ANTIBIOTICS CLINDAMYCIN AND LINCOMYCIN WITH ESCHERICHIA-COLI 23S RIBOSOMAL-RNA [J].
DOUTHWAITE, S .
NUCLEIC ACIDS RESEARCH, 1992, 20 (18) :4717-4720