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Academic Education Mark Brian Anderson, PhD.
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Academic Education Dr. Mark Brian Anderson, PhD ......................
UNIVERSITY OF MASSACHUSETTS 2009:
Clinical Pathology and Nutritional Sciences Department. Professor Eugene Rogers, Program Director. Clinical Pathology Certification Program: Clinical Pathology
combines the theoretical and technical knowledge of human anatomy and physiology, clinical chemistry, genetics, immunology,
microbiology, hematology, histocompatibility, cellular pathology and other fields as they pertain to the dlinical Pathology
combines the theoretical and technical knowledge of human anatomy and physiology, clinical chemistry, genetics, immunology,
microbiology, hematology, histocompatibility, cellpathology and other fields as they pertain to the diagnosis, monitoring
and prevention of disease. HARVARD UNIVERSITY DECEMBER 1989
- APRIL 1992: NSF Postdoctoral Research Fellow with Professor Yoshito Kishi.
Department of Chemistry
and Chemical Biology: Palytoxin (PTX) is a complex marine natural product with 71 asymmetric centers isolated from
soft coral and is considered to be one of the most toxic non-peptide substances known second to maitotoxin. Palytoxin targets
the sodium-potassium pump protein via binding and "locking" it in a position allowing passive transport of both
the sodium and potassium ions, thereby destroying the ion gradient that is essential for most cells. Toxicity symptoms are
angina-like chest pains, tachycardia, unstable blood pressure, hemolysis, asthma-like breathing difficulties, and exaggerated
T-wave in electreocardiograms wherein these symptoms are rapid and death usually follows in minutes.
Synthesis and purifications of the synthetic bioisostere incorporated
PTX from the palytoxin carboxylic acid (PTC) derived from the selective hydrolysis of the vinylogous urea portion of
PTX. Specially trained in the handling of PTX and PTC from a former Japanese Prof. Kishi group member.
Synthesis
and incorporation of novel vinylogous urea bioisosteres of Palytoxin (PTX) into Palytoxin carboxylic acid (PTC),
and the construction of many Palytoxin model systems. Methods included Kishi's Nickel‑Chromium coupling for the synthesis
of the C‑1 to C‑16 and C‑l to C‑25 Palytoxin model systems, worked on new synthetic building blocks,
and carbon-glycosides. Testing of the novel palytoxin analogs were done at the Harvard University Medical School.
PURDUE UNIVERSITY AUGUST 1984 - DECEMBER 1989: Ph.D., NSF and NIH Graduate Research Associate with Professor
Phil. L. Fuchs on "New Methodologies Directed towards the Total Synthesis of Cytochalasins C & D."
The Cytochalasins can be used as chemical "molecular tools" to better understand actin polymerization,
cell motility, ruffling, cell division, contraction, cell stiffness, cytoskeletal movement and other biological processes.
Constructed many advanced intermediates and novel building blocks employing unique Diels-Alder
reactions, an intramolecular chiral acyl transfer strategy, "tried and true" vinyl sulfone technologies, new cyclopentenylations,
anhydrous cerium (III) chloride methodologies, allylsilanes, "BEST" reagents for nucleophilic and electrophilic
mercaptanylations, silicon and tin.
Teaching Assistant Experience
General Chemistry TA: These courses introduced concepts
such as stoichiometry, prediction of reaction products, thermodynamics, nuclear chemistry, electrochemistry, chemical kinetics,
Conservation of energy, Conservation of mass, Law of constant composition, Gas laws, Solubility, Acid-base chemistry, Chemical
bonding, Chemical equilibria and the basics of physical chemistry.
General Chemistry Laboratory TA:
These courses applied the concepts acquired in the lectures and applied them in a supervised laboratory setting.
Organic Chemistry (Chemistry for Medicine/Health Care Fields): These courses were focused on those entering
the medical and healthcare fields. Topics introduced the study of organic structures, properties, composition, reactions and
preparation (by synthesis or by other means) of chemical compounds that contain carbon, basic nomenclature and an introduction
to compounds that may contain any number of other elements, including hydrogen, nitrogen, oxygen, the halogens as well as
phosphorus, silicon and sulfur.
Organic Chemistry Laboratory TA (Chemistry for Medicine/Health
Care Fields): These courses applied the concepts acquired in the lectures and applied them in a supervised laboratory setting.
Organic Chemistry (Chemistry for Chemistry Majors): These courses were focused on those majoring
in chemistry. Topics include the study of organic structures, properties, composition, reactions and preparation (by synthesis
or by other means) of chemical compounds that contain carbon, nomenclature, examples that contain any number of other elements,
including hydrogen, nitrogen, oxygen, the halogens as well as phosphorus, silicon and sulfur. The study and application of
organic chemistry for medicinal chemistry lie on a continuum, but individuals with interests in these areas have one thing
in common; they seek to understand how chemical structure correlates with biological activity.
UNIVERSITY
OF MINNESOTA AUGUST 1980 - JUNE 1984: B.S. degree in chemistry with a focus on biochemistry and microbiology. Conducted
undergraduate research & thesis (CHM 3499) in the biogenesis of alkaloids (heterocyclic syntheses and plant chemical biology),
the biology of plant natural product syntheses, and secondary plant metabolites with the late Professor Edward Leete (08Feb1992).
Niacin (vitamin B3 or nicotinic acid), is a vitamin that prevents the deficiency disease pellagra. However the
tetrahydronicotinic acids are also proposed as intermediates in the biosynthesis of secondary plant metabolites and alkaloids.
Undergraduate Thesis (CHM 3499): "Studies Directed Toward The Synthesis of 1,2,3,6‑Tetrahydronicotinic
Acid and Retronecine for Their Use In Plant Biomimetic Syntheses", and studies in the biogenesis of alkaloids. Additional
studies were on electrode surface modifications with chemically modified riboflavins for studying the biology and reduction
potential of important enzymes with Professor M. T. Stankovich.
Lakewood Community College/Century
College January 1979 - May 1980 main studies in biology and general credits.
AWARDS, PERSONAL INTERESTS, AND OTHER
Professional Associations:
American Chemical Society New
York Academy of Sciences Association for Molecular Pathology American Society for investigative Pathology
Awards: Agouron Pharmaceuticals President's Award in drug discovery (January 1999).
Associations: Harvard University Club; Harvard Boston Club Member, Harvard
San Francisco Club Member
Strathmore's Who's Who in Leadership and Achievement (2003).
United Who's
Who of Executives and Professionals (2003). Multiple Continuing Education
Certificates (CE).
Personal Interests: Golf, Fly Fishing, Skiing, Travel, Languages (Swedish,
German, French, Spanish), Art, Literature, etc.
Useful Software: MS Word, Front Page, PowerPoint, Adobe, ISIS,
Excel, SciFinder, Spotfire, Pipeline Pilot, Group resource and modeling software Beilstein, ISIS base, Accelrys, Schrodinger,
etc.
REFERENCES
Industrial: Alex
Polinsky Ph.D. (owner of Apolco, in Massachusetts) alex.polinsky@gmail.com and John Musser, Ph.D. (COO at Pharmagenesis) jmusser@pharmagenesis.com
Academic: Professor Yoshito Kishi, Ph.D. kishi@chemistry.harvard.edu at Harvard University http://www.harvard.edu/ and Professor Phil. Fuchs, Ph.D. pfuchs@purdue.edu at Purdue University http://www.purdue.edu/
Additional references available on request.
Professional Character
Recommendations: LinkedIn http://www.linkedin.com/in/markbanderson
Printable CV:
www.markbriananderson.com
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