Counting on natural products for drug design

T Rodrigues, D Reker, P Schneider, G Schneider - Nature chemistry, 2016 - nature.com
Natural products and their molecular frameworks have a long tradition as valuable starting
points for medicinal chemistry and drug discovery. Recently, there has been a revitalization …

Target identification for small bioactive molecules: finding the needle in the haystack

S Ziegler, V Pries, C Hedberg… - Angewandte Chemie …, 2013 - Wiley Online Library
Identification and confirmation of bioactive small‐molecule targets is a crucial, often decisive
step both in academic and pharmaceutical research. Through the development and …

The symbiotic relationship between drug discovery and organic chemistry

OO Grygorenko, DM Volochnyuk… - … A European Journal, 2020 - Wiley Online Library
All pharmaceutical products contain organic molecules; the source may be a natural product
or a fully synthetic molecule, or a combination of both. Thus, it follows that organic chemistry …

Highly enantioselective synthesis and cellular evaluation of spirooxindoles inspired by natural products

AP Antonchick, C Gerding-Reimers, M Catarinella… - Nature …, 2010 - nature.com
In biology-oriented synthesis the underlying scaffold classes of natural products selected in
evolution are used to define biologically relevant starting points in chemical structure space …

Biology-oriented synthesis: harnessing the power of evolution

H Van Hattum, H Waldmann - Journal of the American Chemical …, 2014 - ACS Publications
For scientists to gain a better understanding of nature, biological research is greatly aided by
small-molecule modulators that perturb protein activity without fundamentally altering the …

Natural-product-derived fragments for fragment-based ligand discovery

B Over, S Wetzel, C Grütter, Y Nakai, S Renner… - Nature …, 2013 - nature.com
Fragment-based ligand and drug discovery predominantly employs sp 2-rich compounds
covering well-explored regions of chemical space. Despite the ease with which such …

Asymmetric Catalysis of Diels–Alder Reactions with in Situ Generated Heterocyclic ortho-Quinodimethanes

Y Liu, M Nappi, E Arceo, S Vera… - Journal of the American …, 2011 - ACS Publications
The Diels–Alder reaction is probably the most powerful technology in the synthetic repertoire
for single-step constructions of complex chiral molecules. The synthetic power of this …

Exploring new targets and chemical space with affinity selection-mass spectrometry

R Prudent, DA Annis, PJ Dandliker… - Nature Reviews …, 2021 - nature.com
Affinity selection-mass spectrometry (AS-MS) is a high-throughput screening (HTS)
technique for drug discovery that enables rapid screening of large collections of compounds …

Hypervalent iodine reagents in the total synthesis of natural products

LF Silva Jr, B Olofsson - Natural product reports, 2011 - pubs.rsc.org
Covering: 2008–2010 This report describes the recent applications of hypervalent iodine
reagents in the total synthesis of natural products. The large diversity of high-yielding and …

Bridging the gap between natural product synthesis and drug discovery

NJ Truax, D Romo - Natural product reports, 2020 - pubs.rsc.org
Covering: 1986 to 2020 Natural products are an enduring source of chemical information
useful for probing biologically relevant chemical space. Toward gathering further structure …