Tadeusz Molinski
Organic chemistry of marine natural products, synthesis, NMR, and biomedical applications
Contact Information
Department of Chemistry and Biochemistry
Skaggs School of Pharmacy and Pharmaceutical Sciences
Center for Marine Biotechnology and Biomedicine, SIO
Office: PACH 5100E
Phone: (858) 534-7115
Fax: (858) 822-0386
Email: tmolinsk@ucsd.edu
View group members

Education and Appointments
1984 Ph.D., Australian National University, Canberra, Australia
1979 B.S., Monash University, Melbourne

Awards and Academic Honors
2009 President, American Society of Pharmacognosy
2006 Albert Hofmann Centennial Prize, University of Zürich
2004 Chair, Gordon Conference, Marine Natural Products

Research Interests
Marine natural products (MNP's) are chemically-diverse compounds found in marine organisms, such as marine sponges, ascidians, algae and molluscs. Many MNP's have complex molecular structures with multiple elements stereocenters, the presence of halogen (Cl, Br, I) and exotic functional groups. Our group investigates the structure, synthesis and biological properties of novel MNP's. Recent results include discovery of compounds that inhibit cancer cell growth or survival pathways that render cancer cells prone to programmed cell death (apoptosis) and may be useful as drug leads for treatment of human disease.
Fungal infections in individuals with with weakened immune systems such as AIDS patients or those undergoing chemotherapy including are caused by Candida and Cryptococcus and other species. We have discovered compounds that may prove useful in understanding the progression of fungal disease and its treatment.
An outstanding challenge in modern natural products is development of spectroscopic tools that push the limits of detection with vanishingly small quantities of organic compounds. In our nanomole-scale natural products program, we are developing tools which integrate analysis using micro-NMR (e.g. 1.7 mm cryoprobe), chiroptical spectroscopy, particularly circular dichroism (CD), and mass spectrometry for determining absolute configuration of natural products available in amounts <10 nanomole. Funded for our research is from the National Institutes of Health.
Primary Research Area: Interdisciplinary Specialties:
Organic Chemistry Bioorganic
Synthesis


Image Gallery:
Figure 1: Hemiphorboxazole from Phorbas sp. (Indian ocean) Figure 2: Muironolide A from Phorbas sp. (Indian ocean)
Figure 3: Phorbas amaranthus

Selected Publications
  • Masuno MN, Pessah IN, Olmstead MM, Molinski TF, "Simplified cyclic analogues of bastadin-5. Structure-activity relationships for modulation of the RyR1/FKBP12 Ca2+ channel complex." J Med Chem 15(4497-511): , 2006. [Go to PubMed]
  • Skepper CK, Macmillan JB, Zhou GX, Masuno MN, Molinski TF, "Chlorocyclopropane macrolides from the marine sponge Phorbas sp. assignment of the configurations of phorbasides A and B by quantitative CD." J Am Chem Soc 14(4150-1): , 2007. [Go to PubMed]
  • Rogers EW, Dalisay DS, Molinski TF, "(+)-Zwittermicin A: assignment of its complete configuration by total synthesis of the enantiomer and implication of D-serine in its biosynthesis." Angew Chem Int Ed Engl 42(8086-9): , 2008. [Go to PubMed]
  • Molinski TF, Dalisay DS, Lievens SL, Saludes JP, "Drug development from marine natural products." Nat Rev Drug Discov 1(69-85): , 2009. [Go to PubMed]
  • Pigza JA, Quach T, Molinski TF, "Oxazoline-oxazinone oxidative rearrangement. divergent syntheses of (2S,3S)-4,4,4-trifluorovaline and (2S,4S)-5,5,5-Trifluoroleucine." J Org Chem 15(5510-5): , 2009. [Go to PubMed]
  • Dalisay DS, Quach T, Nicholas GN, Molinski TF, "Amplification of the Cotton effect of a single chromophore through liposomal ordering-stereochemical assignment of plakinic acids I and J." Angew Chem Int Ed Engl 24(4367-71): , 2009. [Go to PubMed]
  • Mulder RJ, Shafer CM, Dalisay DS, Molinski TF, "Synthesis and structure-activity relationships of bengazole A analogs." Bioorg Med Chem Lett 11(2928-30): , 2009. [Go to PubMed]
  • Dalisay DS, Molinski TF, "Structure elucidation at the nanomole scale. 2. Hemi-phorboxazole A from Phorbas sp." Org Lett 9(1967-70): , 2009. [Go to PubMed]
  • Morinaka BI, Pawlik JR, Molinski TF, "Amaroxocanes A and B: Sulfated Dimeric Sterols Defend the Caribbean Coral Reef Sponge Phorbas amaranthus from Fish Predators." J Nat Prod (): , 2009. [Go to PubMed]
  • Dalisay DS, Morinaka BI, Skepper CK, Molinski TF, "A tetrachloro polyketide hexahydro-1H-isoindolone, muironolide A, from the marine sponge Phorbas sp. natural products at the nanomole scale." J Am Chem Soc 22(7552-3): , 2009. [Go to PubMed]