Gary Dewayne Probst

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1994-2001 Chemistry Stanford University, Palo Alto, CA 
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Barry M. Trost grad student 1994-2001 Stanford
 (A formal synthesis of alternaric acid and synthetic studies into the mycalamides, onnamides, and theopederins.)
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Franzini M, Ye XM, Adler M, et al. (2013) Triazolopyridazine LRRK2 kinase inhibitors. Bioorganic & Medicinal Chemistry Letters. 23: 1967-73
Garofalo AW, Adler M, Aubele DL, et al. (2013) Discovery of 4-alkylamino-7-aryl-3-cyanoquinoline LRRK2 kinase inhibitors. Bioorganic & Medicinal Chemistry Letters. 23: 1974-7
Garofalo AW, Adler M, Aubele DL, et al. (2013) Novel cinnoline-based inhibitors of LRRK2 kinase activity. Bioorganic & Medicinal Chemistry Letters. 23: 71-4
Bowers S, Truong AP, Neitz RJ, et al. (2011) Design and synthesis of a novel, orally active, brain penetrant, tri-substituted thiophene based JNK inhibitor. Bioorganic & Medicinal Chemistry Letters. 21: 1838-43
Probst GD, Bowers S, Sealy JM, et al. (2011) Highly selective c-Jun N-terminal kinase (JNK) 2 and 3 inhibitors with in vitro CNS-like pharmacokinetic properties prevent neurodegeneration. Bioorganic & Medicinal Chemistry Letters. 21: 315-9
Hom RK, Bowers S, Sealy JM, et al. (2010) Design and synthesis of disubstituted thiophene and thiazole based inhibitors of JNK. Bioorganic & Medicinal Chemistry Letters. 20: 7303-7
Kasibhatla SR, Bookser BC, Probst G, et al. (2010) ChemInform Abstract: AMP Deaminase Inhibitors. Part 3. SAR of 3-(Carboxyarylalkyl)coformycin Aglycon Analogues. Cheminform. 31: no-no
TROST BM, PROBST GD, SCHOOP A. (2010) ChemInform Abstract: Ruthenium-Catalyzed Alder Ene Type Reactions. A Formal Synthesis of Alternaric Acid. Cheminform. 30: no-no
Trost BM, Yang H, Probst GD. (2004) A formal synthesis of (-)-mycalamide A. Journal of the American Chemical Society. 126: 48-9
Trost BM, Probst GD, Schoop A. (1998) Ruthenium-catalyzed alder ene type reactions. A formal synthesis of alternaric acid Journal of the American Chemical Society. 120: 9228-9236
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