Access to a Structurally Complex Compound Collection via Ring Distortion of the Alkaloid Sinomenine

被引:57
作者
Garcia, Alfredo [1 ]
Drown, Bryon S. [1 ]
Hergenrother, Paul J. [1 ]
机构
[1] Univ Illinois, Dept Chem, Roger Adams Lab, 600 South Mathews Ave, Urbana, IL 61801 USA
关键词
PROTEIN-PROTEIN INTERACTIONS; SMALL-MOLECULE INHIBITORS; PRODUCT-LIKE SCAFFOLDS; NATURAL-PRODUCTS; DIVERSE COMPOUNDS; ORIENTED SYNTHESIS; DERIVATIVES; DISCOVERY; MODULATORS; STRATEGY;
D O I
10.1021/acs.orglett.6b02333
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Many compound collections used in high-throughput screening are composed of members whose structural complexity is considerably lower than that of natural products. We previously reported a strategy for the synthesis of complex and diverse small molecules from natural products using ring-distortion reactions, called complexity-to-diversity (CtD), and herein, CtD is applied in the synthesis of 16 diverse scaffolds and 65 total compounds from the alkaloid natural product sinomenine. Chemoinformatic analysis shows that these compounds possess complex ring systems and marked three-dimensionality.
引用
收藏
页码:4852 / 4855
页数:4
相关论文
共 39 条
[1]   Small-Molecule Inhibitors of Protein-Protein Interactions: Progressing toward the Reality [J].
Arkin, Michelle R. ;
Tang, Yinyan ;
Wells, James A. .
CHEMISTRY & BIOLOGY, 2014, 21 (09) :1102-1114
[2]   Small-molecule inhibitors of protein-protein interactions: Progressing towards the dream [J].
Arkin, MR ;
Wells, JA .
NATURE REVIEWS DRUG DISCOVERY, 2004, 3 (04) :301-317
[3]   Expanding medicinal chemistry space [J].
Barker, Andy ;
Kettle, Jason G. ;
Nowak, Thorsten ;
Pease, J. Elizabeth .
DRUG DISCOVERY TODAY, 2013, 18 (5-6) :298-304
[4]   A planning strategy for diversity-oriented synthesis [J].
Burke, MD ;
Schreiber, SL .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2004, 43 (01) :46-58
[5]   Short, Enantioselective Total Syntheses of (-)-8-Demethoxyrunanine and (-)-Cepharatines A, C, and D [J].
Chuang, Kangway V. ;
Navarro, Raul ;
Reisman, Sarah E. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2011, 50 (40) :9447-9451
[6]   A new and efficient one-pot synthesis of apomorphine and its ring-a halogenated derivatives [J].
Csutoras, C ;
Berenyi, S ;
Makleit, S .
SYNTHETIC COMMUNICATIONS, 1996, 26 (12) :2251-2256
[7]   A biosynthesis-inspired approach to over twenty diverse natural product-like scaffolds [J].
Firth, James D. ;
Craven, Philip G. E. ;
Lilburn, Matthew ;
Pahl, Axel ;
Marsden, Stephen P. ;
Nelson, Adam .
CHEMICAL COMMUNICATIONS, 2016, 52 (63) :9837-9840
[8]   Remodeling of Fumagillol: Discovery of an Oxygen-Directed Oxidative Mannich Reaction [J].
Grenning, Alexander J. ;
Snyder, John K. ;
Porco, John A., Jr. .
ORGANIC LETTERS, 2014, 16 (03) :792-795
[9]   Cepharatines A-D, Hasubanan-Type Alkaloids from Stephania cepharantha [J].
He, Li ;
Zhang, Yuan-Hu ;
Guan, Huan-Yu ;
Zhang, Jian-Xin ;
Sun, Qian-Yun ;
Hao, Xiao-Jiang .
JOURNAL OF NATURAL PRODUCTS, 2011, 74 (02) :181-184
[10]   Synthesis of Bridged Oxafenestranes from Pleuromutilin [J].
Hicklin, Robert W. ;
Lopez Silva, Tania L. ;
Hergenrother, Paul J. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2014, 53 (37) :9880-9883