Building New Drugs Just Got Easier LA JOLLA, CA March 12, 2014 Scientists at The Scripps Research Institute (TSRI) have developed a method for modifying organic molecules that significantly expands the possibilities for developing new pharmaceuticals and improving old ones.
This is a technology that can be applied directly to many medicinally relevant compounds, said Jin-Quan Yu, a professor in TSRI's Department of Chemistry and the senior author of the new report, which appears in Nature March 13, 2014.
The innovation makes it easier to modify existing organic compounds by attaching biologically active functional group to drug molecules. A typical small-molecule drug derives its activity from such functional groups, which are bound to a relatively simple backbone structure consisting chiefly of carbon atoms.
Pushing the Boundaries
Chemists over the past half-century or so have devised various methods for adding functional groups to carbon atoms, to make new compounds and to modify old ones. But a certain type of modification has remained largely out of reach.
Known as a meta C-H activation, this modification involves the temporary attachment of a helper molecule to one carbon atom, in such a way that the helper molecule extends past the nearest-neighbor carbon atom to the next-nearest carbon atom, and there mediates the addition of a functional group. It is a tricky task for a number of reasons, but mostly because the targeted attachment site is so far away and inaccessible. The carbon in the backbone of a typical organic compound is arranged in rings of six or so carbon atoms and thus to reach from one such carbon over a second to a third means reaching almost to the far side of the ring.
In 2012, Yu and his colleagues published a landmark paper, also in Nature, which described a way to accomplish this feat with one set of compounds. They devised a helper molecule, with a long segment called a nitrile, that could attach to one carbon atom on the compound, arch over the next-door carbon atom, and in effect swing a palladium atom at its far end back a bit like a crane swinging a wrecking ball to the targeted carbon atom. There the palladium atom would act as a catalyst to dislodge the existing occupant, a hydrogen atom, enabling the attachment of the new functional group.
Following the same principle, Yu's team recently came up with a new template for making meta-C-H activations on a much more challenging set of organic compounds. Now, in the new study, the researchers have demonstrated the same task with a major family of compounds known as amines, including medicinally important heterocyclic amines. In so doing, the researchers found a way to use a helper molecule also called a template that is chemically simpler and more user-friendly than the ones they have described in previous work.
A Boost to Drug Discovery
Unusually for such a project, the TSRI chemists analyzed the 3D atomic structure of their template compound using X-ray crystallography as well as nuclear magnetic resonance spectroscopy. These studies revealed that the new template's ability to mediate the attachment of a new functional group to a distant carbon atom can be tuned by making slight changes to its chemical composition, including the choice of the proper metal catalyst at its working end.
The key is to tune the shape of the template to create a subtle bias towards the targeted carbon hydrogen bond, said Yu. At the same time the template's movement towards the target site has to be exploited effectively by a super-reactive catalyst.
Compounds that can be modified using the new technique include tetrahydroquinoline, benzooxazines, anilines, benzylamines, 2-phenylpyrrolidines and 2-phenylpiperidines. All these are commonly used in medicinal chemistry either as final drug compounds or intermediate compounds from which the final compounds are made, Yu said.
Yu is now collaborating with the pharmaceutical company Bristol-Myers Squibb to use his meta-C-H activation techniques to make potential new drug compounds.
Techniques like this one that enable controlled, remote C-H activation are just beginning to be adopted by industry, and should provide a boost to drug discovery and development efforts for many years to come, Yu said.
The other authors of the study, Conformation-Induced Remote meta-C H Activation of Amines, were Ri-Yuan Tang (lead author) and Gang Li, respectively a visiting professor and a research associate at TSRI during the study.
The study was supported by the National Institute of General Medical Sciences, part of the National Institutes of Health (1R01 GM102265).
About The Scripps Research Institute
The Scripps Research Institute (TSRI) is one of the worlds largest independent, not-for-profit organizations focusing on research in the biomedical sciences. TSRI is internationally recognized for its contributions to science and health, including its role in laying the foundation for new treatments for cancer, rheumatoid arthritis, hemophilia, and other diseases. An institution that evolved from the Scripps Metabolic Clinic founded by philanthropist Ellen Browning Scripps in 1924, the institute now employs about 3,000 people on its campuses in La Jolla, CA, and Jupiter, FL, where its renowned scientists including three Nobel laureates work toward their next discoveries. The institutes graduate program, which awards PhD degrees in biology and chemistry, ranks among the top ten of its kind in the nation. For more information, see www.scripps.edu.
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For information:
Office of Communications
Tel: 858-784-2666
Fax: 858-784-8136
press@scripps.edu
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Building New Drugs Just Got Easier LA JOLLA, CA March 12, 2014 Scientists at The Scripps Research Institute (TSRI) have developed a method for modifying organic molecules that significantly expands the possibilities for developing new pharmaceuticals and improving old ones.
