CURRICULUM VITAE
PERSONAL INFORMATION
Name: Michael E. Jung
Date and Place of Birth: May 14, 1947 in New Orleans, Louisiana
Marital Status: Married, wife Alice
Mailing Address: Department of Chemistry
University of California
Los Angeles, CA 90095-1569
Telephone: (310) 825-7954 FAX: (310) 206-3722
email: jung@chem.ucla.edu
EDUCATIONAL BACKGROUND
Distinguished Professor, UCLA, 2004 - present
Professor Further Above Scale, UCLA, 2002 - 2004
Professor Above Scale, UCLA, 1998 - 2002
Professor VIII, UCLA, 1996 - 1998
Professor VII, UCLA, 1994 - 1996
Professor VI, UCLA, 1992 - 1994
Professor V, UCLA, 1990 - 1992
Professor IV, UCLA, 1988 - 1990
Professor III, UCLA, 1987 - 1988
Professor II, UCLA, 1985 - 1987
Professor I, UCLA, 1983 - 1985
Associate Professor III, UCLA, 1981 - 1983
Associate Professor I, UCLA, 1979 - 1981
Assistant Professor IV, UCLA, 1977 - 1979
Assistant Professor III, UCLA, 1976 - 1977
Assistant Professor II, UCLA, 1974 - 1976
NATO Postdoctoral Fellowship, Eidgenössische Technische Hochschule, Zürich, Switzerland, 1973 - 1974; Albert Eschenmoser, advisor
Ph.D., Columbia University, New York, New York, 1973; Gilbert Stork, advisor
B.A., Summa cum laude, Rice University, Houston, Texas, 1969; Richard Turner, advisor
PROFESSIONAL AFFILIATION
American Chemical Society, 1969 - present
The Chemical Society, 1971 - present
Phi Lambda Upsilon, 1968 - present
UCLA Cancer Center, 1975 - present
Division of Organic Chemistry, ACS, 1975 - present
Division of Medicinal Chemistry, ACS, 1975 - present
Sigma Xi, 1977 - present
American Men and Women of Science, Chemistry, 1977 - present
American Association for the Advancement of Science, 1979 – present
Molecular Biology Institute, UCLA, 2004 - present
California
NanoSystems Institute (CNSI), UCLA, 2006 - present.
Director, UCLA Biosciences Synthetic Chemistry Core Facility
COWORKERS
Current: 12 graduate students, 7 postdoctoral associates, 1 undergraduate
Former: 76 PhD's granted, 7 MS's granted, 98 postdoctoral associates, 40 undergraduates, 21 research associates and technicians
HONORS AND AWARDS
Professional - University of California
2008
Plenary Lecturer, Organic Synthesis Symposium, 43rd Mexican Chemical
Society
National Meeting, Tijuana, Mexico
2008 Plenary
Lecturer, Symposium in honor
of Victor Marquez, American Chemical Society
National Meeting, Philadelphia, PA
2008 Plenary Lecturer, Symposium on Organic Synthesis, 91st National Meeting
of the Canadian Society for Chemistry, Edmonton, Canada2006 Boehringer-Ingelheim Lecturer, University of British Columbia, Vancouver
2004 Plenary
Lecturer, Ischia Advanced School of Organic
Chemistry, Ischia, Italy
2004
Bristol-Myers Squibb Lecturer, University of Puerto Rico, Rio Piedras,
PR
2003 Invited Professor, Université Pierre et Marie Curie, Paris
2002 Auspex Horizon Award, Auspex Pharmaceutical Co., Inc., San Diego, CA
2002 Plenary Lecturer, 60th Anniversary International Symposium
on Organic Synthesis, Tokyo, Japan2001 Plenary Lecturer, First International Symposium on Asymmetric Synthesis
Universidad Nacional Autonoma de Mexico (UNAM), Mexico City1999 Plenary Lecturer, Japan Pharmaceutical Society, Tokushima, Japan
1999 Plenary Lecturer, Japan Chemical Society, Tokyo, Japan
1998 Plenary Lecturer, 21st Gulf Coast Chemistry Conference, Pensacola, FL
1998 Invited Lecturer, XIII International Round Table on Nucleosides, Nucleotides
and Their Biological Applications, Montpellier, France
1998 Invited Lecturer, 19th International Carbohydrate Symposium, La Jolla, CA
1998 Plenary Lecturer, Western Switzerland Lecture Tour
1998 Plenary Speaker, Spring Meeting, French Chemical Society, Paris
1998 Plenary Lecturer, Robert A. Welch Foundation
1997 Plenary Speaker, 2nd AFMC International Medicinal Chemistry Symposium
(AIMECS 97), Seoul
1997 Invited Lecturer, 16th International Congress of Heterocyclic Chemistry,
Montana State University, Bozeman, MT
1995 American Chemical Society Arthur C. Cope Scholar Award
1995 Plenary Lecturer, Gordon Conference on Purines, Pyrimidines,
and Other Related Substances
1995 Plenary Lecturer, 5th French American Chemical Society (FACS) Conference
1992 Hanson-Dow Teaching Award, UCLA
1991 Herbert Newby McCoy Award Recipient, UCLA
1991 Fujii-Ohtsuka Professor, University of Tokushima, Tokushima, Japan
1988 Plenary Lecturer, 3rd Nozaki Conference, Sagamihara, Japan
1987 Glenn T. Seaborg Award Recipient
1987
Plenary
Lecturer, Gordon Conference on Natural
Products Chemistry
1987 Plenary Lecturer, Gordon Conference on Organic Reactions and Processes
1986 Inaugural UCLA Gold Shield Faculty Prize
1985 Plenary Lecturer, 9th Oxford Symposium on Organic Synthesis, Oxford
1982 Plenary Lecturer, 4th International Conference on Organic Synthesis, Tokyo
1981 Invited
Participant, Twelfth Annual Workshop on
Organic Synthesis in 1978
Invited
Speaker, Symposium for Creative Work in
Synthetic Organic
Chemistry,
175th ACS National Meeting, Anaheim 1978
Plenary
Lecturer, 5th Annual Conference on
Organosilicon Chemistry 1977
Invited
Participant, Eight Annual Workshop on Organic Synthesis in Natural
Products
Chemistry, Dartmouth College Minary Conference Center, NH 1975
UCLA Summer
Faculty Fellow
Natural
Products Chemistry, Pingree Park, Colorado
1981 Plenary
Lecturer, French Chemical Society Meeting,
Paris (Spring)
1980 Fulbright-Hays
Grant, U.S. Research Scholar Award
1980 American Cyanamid
Young
Researcher Award
1980 Plenary
Lecturer, Gordon Conference on
Organometallic Chemistry
1979 Alfred
P. Sloan Foundation Research Fellow
1979 Camille and
Henry Dreyfus Teacher-Scholar
Grantee
1977 Eli
Lilly Grantee
1978 University
Distinguished Teaching Award
Postgraduate
- Eidgenössische Technische
Hochschule
1973
Hammett
Award for Research
Graduate
- Columbia University
Undergraduate
- Rice University
1968 Phi Beta Kappa
1967-69 ARCS Foundation Scholar
1967-68 Blanche White Honor Scholar
1966-67 William Marsh Rice Scholar
1965-66 University Prize Scholar
MEMBERSHIP ON
SCIENTIFIC ADVISORY BOARDS
Neurocrine Biosciences, Inc., La Jolla, CA, 2003 - present
Auspex Pharmaceuticals, Inc., Vista, CA, 2004 - present
Medivation, Inc., San Francisco, CA, 2006 - present
Trius Pharmaceuticals (formerly Rx3 Pharmaceuticals), San Diego, CA, 2006 - present
Encore
Pharmaceutical, Inc., Loma Linda, CA, 1998 - 2002
CONSULTANTSHIPS
Wyeth
Research, Inc.
(formerly
Wyeth-Ayerst, American Home Products (AHP), American
Cyanamid Company,
Lederle
Laboratories), Pearl River, NY, 1988 - present
Wyeth Research, Inc. (formerly AHP Medical Research Div.), Princeton, NJ, 1995 - present
Wyeth Research, Inc., Collegeville, PA (formerly Radnor, PA), 1998 - present
Wyeth Research, Inc. (formerly Genetics Institute), Cambridge, MA, 2001 - present
ORIL, S.A., Bolbec, France, 1996 - present
Gilead Science Process Chemistry, Foster City, CA, 1996 - present
Gilead Science Medicinal Chemistry, Foster City, CA, 1999 - present
Neurocrine Biosciences, Inc., La Jolla, CA, 1999 - present
Institut de Recherche Servier, Servier Pharmaceutical Inc., Suresnes, France, 2000 - present
DuPont Crop Protection, Newark, DE, 2002 - present
Alnylam, Inc., Cambridge, MA, CA, 2003 - present
Ardea Pharmaceutical
(formerly
Valeant), San
Diego, CA, 2003 - present
Cylene Pharmaceuticals, San Diego, CA, 2003 - present.
Celgene Pharmaceutical, Inc., San Diego, CA, 2003 - present
Auspex Pharmaceuticals, Inc., Vista, CA, 2004 - present
ArQule Pharmaceutical Inc., Woburn, MA, 2005 - present
Abraxis BioSciences, Inc., Santa Monica, CA, 2005 - present
Trius Pharmaceuticals
(formerly Rx3
Pharmaceuticals), San Diego, CA 2006 -
present
ZaCh System, Inc. (formerly PPG-Sipsy), Angers, France 2007 - present
Medivation, Inc., San
Francisco, CA
2007 - present
Prestwick Chemicals,
Inc., Strasbourg,
France 2007 - present
SePRO, Inc.,
Indianapolis, IN,
1998-2000, 2007 - present
Critical Therapeutics,
Inc.,
Lexington, MA 2007 - present
GlaxoSmithKline (GSK)
Pharmaceuticals,
Inc., Collegeville, PA 2008 - present
GlaxoSmithKline (GSK)
Pharmaceuticals,
Inc., Res. Triangle Park, NC, 2008 - present
Vertex Pharmaceutical,
San Diego, CA,
2008 - present
Orphagen
Pharmaceuticals, San Diego,
CA 2008 - present
CacliMedica, Inc., San Diego,
CA 2008 - present
The
majority of the research personnel in my group are currently engaged in
three general fields of interest: the
development of new synthetic methods, the total synthesis of
biologically active natural products, and medicinal chemistry. We are
pursuing the total synthesis of potent antiviral agents, e.g., modified
nucleosides
and betulinic acid derivatives, several promising antitumor agents,
e.g.,
tedanolide and 13-deoxytedanolide, eleutherobin, dichlorolissoclimide,
haterumaimide E, the auripyrones, and laurenediterpenol. The use of
epoxide
rearrangements in synthesis, e.g., the non-aldol aldol process, and
others, is under
investigation as well, especially for the synthesis of new antibiotics
of the erythromycin class. We are also studying the use of various
reactions (e.g., Diels-Alder reactions, bridged Robinson annulation,
[3,3]
rearrangements) for the synthesis of biologically active molecules,
e.g., the acetylcholinesterase inhibitors, the arisugacins; the
immunosuppressive
agent brasilicardin A; the antibacterial agent mycosporulone; and
multiple drug resistance
reversing agents such as welwitindolinone C. In particular, we are
developing the mixed Lewis acid system, 5-10:1 AlBr3:AlMe3,
in a variety of reactions, e.g.,
cycloadditions, nucleophilic additions, etc. We are developing new
processes for the efficient
synthesis of various oxygenated steroids, e. g., the cardioactive
compound ouabain and the
antitumor compound, rhodexin A. We have several collaborative programs
in medicinal chemistry, e.g., to prepare various naturally occurring
oxidation products of arachidonic acids, the epoxy isoprostanes (which
are
involved in the onset of atherosclerosis); to develop a new method of
delivering
antibacterial agents to resistant bacterial strains; the preparation
and testing of
new selective binders for both the estrogen and the androgen receptors
as
anti-cancer agents; the synthesis of molecules which differentiate stem
cells into
osteoblasts; the preparation of molecules to bind to the Sortase-A
binding pocket to determine the structure of this important medicinal
target; small
molecule inhibitors of the growth of various viruses; and agents to
stop the
growth of tuberculosis.
OTHER PUBLICATIONS
1. M. E. Jung, "An Improved Procedure for the Conversion of Amines to Alcohols at Low Temperature; New Synthesis of Alkenes and Alkynes from Amines," Chemtracts 1990, 3, 392.
2. M. E. Jung, "Iodomethyl Methyl Ether," Encyclopedia of Reagents for Organic Synthesis, John Wiley & Sons, Ltd., 1995.
3. M. E. Jung, "Trimethylsilyl iodide," Encyclopedia of Reagents for Organic Synthesis, John Wiley & Sons, Ltd., 1995.
4. M. E. Jung, "1-Trimethylsilyloxy-1,3-butadiene," Encyclopedia of Reagents for Organic Synthesis, John Wiley & Sons, Ltd., 1995.
5. M. E. Jung, "2-Trimethylsilyloxy-1,3-butadiene," Encyclopedia of Reagents for Organic Synthesis, John Wiley & Sons, Ltd., 1995.
6. M. E. Jung, "Triphenylcarbenium Tetrafluoroborate," Encyclopedia of Reagents for Organic Synthesis, John Wiley & Sons, Ltd., 1995.
7. W. J. Wechter, E. D. Murray, Jr., D. Kantoci, and M. E. Jung, "Characterization of Two New Endogenous Natriuretic Factors," Abstract, 29th Annual Meeting, American Society of Neurology, November 1996.
8. Crostic No. 49 in Crostics, No. 115, Simon & Schuster, New York, NY, ed. T. H. Middleton, 1996.
9. S. E. Denmark, M. E. Jung, A. Pfaltz, B. Giese, "Laudio for Professor Doctor Albert Eschenmoser," Synlett 1999, III.
10.
M. E. Jung, "Tungsten Hexachloride," Encyclopedia
of Reagents for Organic Synthesis,
John Wiley
& Sons, Ltd., 2006.
MEETING ABSTRACTS
1. Richardson, J. A.;
Amantea, C. M.;
Nguyen, K.; Jung, M. E.; Hahn, T. J.; Parhami, F. "Characterization of
osteogenic oxysterols and their molecular mechanism(s) of
action,"� J. Bone Mineral Res.
2005, 20, S414-S415 Suppl.
1.
2. Wechter, W. J.;
Murray, E. D.; Kantoci, D.; Jung, M. E. "Characterization of two new
endogenous natriuretic
factors," J. Am.
Soc. Nephrol. 1996, 7, A2867-A2867.
SHORT COURSES
1. Nov. 1980: Upjohn Co., Kalamazoo, MI, "New Advances in the Use of Diels-Alder Reactions in Synthesis."
2. Sept. 1985: American Cyanamid Co., Agricultural Research Division, Princeton, NJ, "Silicon in Organic Synthesis."
3. Sept. 1987: Zhongshan University, Guangzhou, PRC, "Modern Organic Synthesis."
4. Sept. 1987: Zhongshan University, Guangzhou, PRC, "Silicon in Organic Synthesis."
5. April 1996: 3M, St. Paul, MN, "Strategy and Design in Organic Synthesis."
6. April 1998: 3M, St. Paul, MN, "New Methods in Heterocyclic Chemistry."
7. Dec. 1999: Neurocrine Biosciences, "Introduction to Modern Heterocyclic Chemistry."
8. Mar. 2003: Université Pierre et Marie Curie, Paris, "Modern Heterocyclic Chemistry."
9. May 2008:
Vertex, Inc., San Diego, "Modern Heterocyclic Chemistry."
PATENTS AND
APPLICATIONS
1.
Cross, B.; Los, M.; Doehner, R. F., Jr.;
Ladner, D. W.; Johnson, J. L.; Jung, M. E.; Kamhi, V. M.; Tseng, S. S.;
Finn, J. M.; Wepplo, P. J. (Assignee: American Cyanamid Company)
"Preparation of Novel Fused Imidazolinylpyridines as
Herbicides,"� Eur.
Pat. Appl. 1987, EP 227932 A1.
2. Jung, M. E.; Gardiner, J. M.
(Assignee: The
Regents of the University of California) "Process for
the Synthesis of 2',3'-Dideoxynucleosides," US
Patent 5,220,003 (June 15, 1993).
3.
Cross, B.; Los, M.; Doehner, R. J., Jr.; Ladner, D. W.;
Johnson,
J. L.;
Jung, M. E.; Kamhi, V. M.; Tseng, S.-S.; Finn, J. M.; Wepplo, P. J.
(Assignee: American Cyanamid
Company) "(2-Imidazolin-2-yl) Fused Heteropyridine Compounds,
Intermediates for
the Preparation of and Use of Said Compounds as Herbicidal
Agents," US
Patent 5,252,538 (October 12,
1993).
4. Harrington, P. E.; Jung, M. E. (Assignee: American Cyanamid Company) "Stereoselective Bromination of β-Ribofuranosyl Amide: Synthesis of Herbicidal Analogues of Hydantocidin," US Patent 5,354,868 (October 11, 1994).
5.
Jung, M. E.; D'Amico, D. C.
(Assignee:
The Regents of the University of California)
"Stereospecific
Synthesis of Aldols," US Patent 5,426,206
(June 20, 1995).
6. Harrington, P. E.; Jung, M. E. (Assignee: American Cyanamid Company) "Process and Intermediates for the Preparation of (+)-Hydantocidin and Analogs Thereof ," US Patent 5,543,510 (August 6, 1996).
7. Jung, M. E.; Cook, P. D.; Kawasaki, A. M. (Assignee: Isis Pharmaceuticals) "Method for Removing Unreacted Electrophiles from a Reaction Mixture," US Patent 5,632,898 (May 27, 1997).
8. Fraser, A. S.; Manoharan, M.; Cook, P. D.; Jung, M. E.; Kawasaki, A. M. (Assignee: Isis Pharmaceuticals) "Alkylation of Alcohols, Amines, Thiols and Their Derivatives by Cyclic Sulfate Intermediates," US Patent 6,277,982 (August 21, 2001).
9. Manoharan, M.; Guzaev, A.; Jung, M. E.; Just, G.; Roland, A.; Wang, J. (Assignee: Isis Pharmaceuticals) "Oligonucleotides having Alkylphosphonate Linkages and Methods for Their Preparation," US Patent 6,486,313 (November 26, 2002).
10.
Jung,
M. E.; Xu, Y. (Assignee:
The Regents of the University of California) "Process for
the Synthesis
of L-Ribose and 2-Deoxy-L-Ribose," Application
Abandoned.
11. Manoharan, M.; Just, G.; Guzaev, A.; Roland, A.; Wang, J.; Jung, M. E. (Assignee: Isis Pharmaceuticals) "Solid Phase Synthesis of Alkylphosphonate-linked Oligodeoxyribonucleotides," PCT Int. Appl. (2000), WO 0049032.
12. Finn, J.; Morytko, M.; Parr, I. B.; Jung, M. E. (Assignee: Cubist Pharmaceuticals) "Preparation of novel depsipeptides as antibacterials," PCT Int. Appl. (2003), WO 0314147.
13. Morytko, M.; Zhang, Y.; Jung, M. E.; Finn, J.; Bouchard, M. (Assignee: Cubist Pharmaceuticals) "Preparation of lipopeptide stereoisomeric compounds as antibacterial agents," PCT Int. Appl. (2003), WO 0317924.
14. Jung, M. E.; Ouk, S.; Sawyers, C. L.; Chen, C. D.; Welsbie, D. (Assignee: The Regents of the University of California) "Preparation and Activity of Novel Prostate Cancer Drugs," US Provisional Patent Appl., G&C 30435.158-US-P1, Feb. 24, 2004.
15. Sawyers, C. L.; Jung, M. E.; Chen, C. D.; Ouk, S.; Welsbie, D. (Assignee: The Regents of the University of California) "Novel Androgen Receptor Inhibitors with Minimal Agonistic Activities," US Provisional Patent Application, 60/680,835, May 11, 2005.
16. Manoharan, M.; Jung, M. E.; Rajeev, K. G.; Pandey, R. K.; Wang, G. (Assignee: Alnylam Pharmaceuticals) "Processes and Reagents for Oligonucleotide Synthesis and Purification," US Provisional Patent Application, 11/099,430, April 5, 2005.
17. Whitten, J. P.; Pierre, F.; Regan, C.; Schwaebe, M.; Yiannikouros, G. P.; Jung, M. E. (Assignee: Cylene Pharmaceuticals) "Novel Benzothiazole Compounds and methods of Use Thereof," US Provisional Patent Application, 11/149,007, June 9, 2005. U.S. Pat. Appl. Publ. 2006, US 2006063761.
18. Manoharan, M.; Jung, M. E.; Rajeev, K. G.; Pandey, R. K.; Wang, G. (Assignee: Alnylam Pharmaceuticals) "Process and phosphoramidation reagents for oligonucleotide synthesis and purification," PCT Int. Appl. 2005, WO 2005097817.
19.
Jung, M. E.; Ouk, S.; Sawyers,
C. L.; Chen, C. D.; Welsbie,
D. (Assignee: The
Regents of the University of California)
"Androgen receptor-based methods and materials for assessing
prostate cancer therapies, and compounds," PCT Int. Appl. (2005), WO
2005099693.
20. Whitten, J. P.; Pierre, F.; Regan, C.; Schwaebe, M.; Yiannikouros, G. P.; Jung, M. E., Nagasawa, J. Y.; Chua, P. (Assignee: Cylene Pharmaceuticals) "Process for the Preparation of Benzothiazole and Phenoxazine Compounds," US Patent Application 2006063761.
21. Whitten, J. P.; Pierre, F.; Regan, C.; Schwaebe, M.; Yiannikouros, G. P.; Jung, M. E. (Assignee: Cylene Pharmaceuticals) "Preparation of fused quinolone analogs which inhibit cell proliferation and/or induce cell apoptosis," PCT Int. Appl., 2006, WO 2006034113.
22. Whitten, J. P.; Pierre, F.; Regan, C.; Schwaebe, M.; Yiannikouros, G. P.; Jung, M. E. (Assignee: Cylene Pharmaceuticals) "Preparation of fused quinolone analogs which inhibit cell proliferation and/or induce cell apoptosis," US Provisional Patent Application, 2006, US 2006074089, Cont.-in-part of U.S. Ser. No. 149,007.
23. Parhami, F.; Jung, M. E.; Nguyen, K.; Dwyer, J. R. (Assignee: The Regents of the University of California) "Synthesis and Regulation of Oxysterols," US Provisional Patent Application, Docket No. 38586-347, February 27, 2006.
24. Sawyers, C. L.; Jung, M. E.; Chen, C. D.; Ouk, S.; Welsbie, D.; Tran, C.; Wongvipat, J.; Yoo, D. (Assignee: The Regents of the University of California) "Preparation of Diarylthiohydantoin Compounds as Androgen Receptor Antagonists Useful against Hormone Refractory Prostate Cancer," PCT International Application 2006, 166 pp. WO 2006124118.
25. Parhami, F.; Jung, M. E.; Dwyer, J. R.; Nguyen, K. (Assignee: The Regents of the University of California) "Preparation of oxysterol compounds that stimulate the hedgehog pathway for treatment of various disorders," PCT International Application 2007, 83 pp. WO 2007098281 A2.
26. Jung, M. E.; Yoo, D.; Sawyers, C. L.; Tran, C. (Assignee: The Regents of the University of California) "Diarylthiohydantoin Compounds," US Patent Application Publication, US 2007254933.
27. Jung, M. E.; Sawyers, Charles L.; Ouk, S.; Tran, C.; Wongvipat, J. (Assignee: The Regents of the University of California) "Androgen Receptor Modulator for the Treatment of Prostate Cancer and Androgen Receptor-associated Diseases," PCT Int. Appl. (2007), WO 2007126765 A2.
INVITED
LECTURES
490 Lectures, seminars, and presentations at international and national chemical meetings and symposia, academic institutions, and industrial institutions from 1973-2008.