Mitochem Therapeutics
President and Chief Executive Officer
Mitohealth
President and Chief Executive Officer
Medical University of South Carolina
Professor
Stanford University 1993 - 1996
Postdoctoral Associate
Education:
Stanford University School of Medicine 1993 - 1996
Uc Irvine 1987 - 1993
Doctorates, Doctor of Philosophy, Organic Chemistry
Skills:
Drug Discovery Molecular Biology Immunology Western Blotting Microscopy Peptide Synthesis Physiology Biophysics Elisa Biotechnology Cancer Pcr Cell Protein Purification Assay Development Animal Models Pharmacology Protein Expression Hplc Cell Biology Polymerase Chain Reaction High Performance Liquid Chromatography
Interests:
Politics Education Environment Science and Technology Health
Bernstein Irwin - Seattle WA, US Peter Senter - Seattle WA, US Craig Beeson - Charleston SC, US Michael Hart - Seattle WA, US
International Classification:
A61K051/00 A61K039/395 C07K016/46
US Classification:
424/178100, 424/001490, 530/391100
Abstract:
A novel bioconjugate and a method for delivering the bioconjugate to a cell site is described. In particular, the bioconjugate composition comprises a targeting agent conjugated to a diagnostically or therapeutically effective agent by a metabolizable linker moiety which is cleaved by an exogenous enzyme.
Giuseppe Gumina - Charleston SC, US Craig Beeson - Charleston SC, US Gary Wright - Charleston SC, US
International Classification:
A61K 31/7076
US Classification:
514045000
Abstract:
Disclosed herein are compounds having Formula I, which are non-natural L-adenosine analogs. Also disclosed are their methods of making. Still further, disclosed are the uses of the disclosed compounds to treat cardiovascular disease, ischemia related injuries, and neurodegenerative diseases.
Compositions And Methods For The Treatment Of Degenerative Diseases
Craig Cano Beeson - Charleston SC, US Baerbel Rohrer - Charleston SC, US Nathan Perron - Charleston SC, US
Assignee:
MUSC Foundation For Research And Development - Charleston SC
International Classification:
C07D 417/14 C07D 401/04 C07D 401/08 C07D 417/04
US Classification:
514339, 435 29, 435375, 514342, 5462704, 5462777
Abstract:
Disclosed are compounds or pharmaceutically acceptable salts thereof, having the structure of formula I. Also disclosed are methods of preventing and/or treating degenerative disease in a subject, comprising administering to said subject a therapeutically effective amount of a compound of formula I, or a pharmaceutically acceptable salt thereof. Also disclosed are pharmaceutical compositions for preventing and/or treating de-generative disease in a subject comprising a therapeutically effective amount of a compound of formula I, or a pharmaceutically acceptable salt thereof.
Craig C. BEESON - Mount Pleasant SC, US Yuri K. PETERSON - James Island SC, US
Assignee:
MUSC Foundation For Research Development - Charleston SC
International Classification:
A61K 31/4704 A61K 31/138 A61K 31/137
US Classification:
514312, 514653, 514651
Abstract:
Methods and compositions for inducing mitochondrial biogenesis are provided. In some aspects, methods for the treatment of diseases such as acute kidney disease (AKI) or a muscle wasting disease by administering tomoxetine, nisoxetine, fenoterol, formoterol, or procaterol to an individual are provided.
5Ht1F Receptor Agonists And Mitochondrial Biogenesis
- Charleston SC, US Craig C. BEESON - Charleston SC, US Yuri Karl PETERSON - Charleston SC, US Rick G. SCHNELLMANN - Tucson AZ, US
International Classification:
C07D 239/47 A61P 13/12
Abstract:
Provided herein are compounds of the formula (I): as well as pharmaceutically acceptable salts thereof, wherein the substituents are as those disclosed in the specification. These compounds, and the pharmaceutical compositions containing them, promote mitochondrial biogenesis and are useful for the treatment of, for example, acute kidney injury and chronic kidney disease.
Silage compositions are described herein, as well as methods for their preparation and use. A silage composition may include a fatty acid component comprising at least about 70% saturated fatty acid by weight and a fermented component. The fatty acid component may be present in the silage composition in an amount of at least about 10% by weight of the silage composition.
Aza-Ellipticine Analogs, Methods Of Synthesis And Methods Of Treatment
- Charleston SC, US Craig C. Beeson - Charleston SC, US
International Classification:
C07D 471/14
Abstract:
In some aspects, the present invention relates to aza-ellipticine compounds of the formula: wherein the variables are as defined herein. The application also provides novel methods of preparing aza-ellipticine compounds, methods of using the compounds, and pharmaceutical compositions thereof.
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