D. R. Cary

发表

Identification of a selective DDX3X inhibitor with newly developed quantitative high-throughput RNA helicase assays.

Masahiro Ito, S. Aparicio, T. Kawamoto, 2020, Biochemical and biophysical research communications.

Ligand-centered oxidation in a diiron s-indacene complex

S. Barlow, D. O′Hare, Jennifer C. Green, 2000 .

New strongly coupled dinuclear metal centres in organometallic s-indacene complexes

S. Barlow, D. O′Hare, Jennifer C. Green, 1997 .

Discovery of Novel 5-(Piperazine-1-carbonyl)pyridin-2(1H)-one Derivatives as Orally eIF4A3-Selective Inhibitors.

K. Fukuda, Y. Imaeda, Y. Kosugi, 2017, ACS medicinal chemistry letters.

Discovery of Novel 1,4-Diacylpiperazines as Selective and Cell-Active eIF4A3 Inhibitors.

Masahiro Ito, S. Aparicio, T. Kawamoto, 2017, Journal of medicinal chemistry.

Studies of CDK 8/19 inhibitors: Discovery of novel and selective CDK8/19 dual inhibitors and elimination of their CYP3A4 time-dependent inhibition potential.

Maki Hasegawa, Kazunobu Aoyama, A. Hata, 2017, Bioorganic & medicinal chemistry.

Design and synthesis of selective CDK8/19 dual inhibitors: Discovery of 4,5-dihydrothieno[3',4':3,4]benzo[1,2-d]isothiazole derivatives.

Hiroshi Banno, Yuka Hasegawa, M. Okaniwa, 2017, Bioorganic & medicinal chemistry.

Unusual reactivity and isomerisation in dicobalt s-indacene complexes

D. O′Hare, Mark J. Drewitt, D. R. Cary, 1998 .

Isostearyl Mixed Anhydrides for the Preparation of N-Methylated Peptides Using C-Terminally Unprotected N-Methylamino Acids.

K. Masuya, Yutaka Kobayashi, N. Nishizawa, 2020, Organic letters.

Synthesis and Characterization of Divalent Lanthanide Selenolates and Tellurolates. X-ray Crystal Structures of Yb[SeSi(SiMe3)3]2(TMEDA)2 and {Eu[TeSi(SiMe3)3]2(DMPE)2}2(.mu.-DMPE)

J. Arnold, D. R. Cary, 1994 .

Fragment-based discovery of nonpeptidic BACE-1 inhibitors using tethering.

Jian Sun, D. M. Penny, Wanli Lu, 2009, Biochemistry.

Trivalent Lanthanide Selenolates and Tellurolates Incorporating Sterically Hindered Ligands and Their Characterization by Multinuclear NMR Spectroscopy and X-ray Crystallography

G. Ball, J. Arnold, D. R. Cary, 1995 .

Preparation of lanthanide tellurolates and evidence for the formation of cluster intermediates in their thermal decomposition to bulk metal tellurides

J. Arnold, D. R. Cary, 1993 .

Rhenium bipyridine complexes for the recognition of glucose.

J. Satcher, S. Lane, W. P. van Antwerp, 2002, Inorganic chemistry.

Selective ion-exchange intercalation of isomeric dicarboxylate anions into the layered double hydroxide [LiAl2(OH)6]Cl.H2O

D. O′Hare, S. Shyu, A. Fogg, 1998 .

TP-064, a potent and selective small molecule inhibitor of PRMT4 for multiple myeloma

K. Saikatendu, C. Arrowsmith, M. Schapira, 2018, Oncotarget.

Design, synthesis, and evaluation of novel VEGFR2 kinase inhibitors: discovery of [1,2,4]triazolo[1,5-a]pyridine derivatives with slow dissociation kinetics.

M. Tawada, Naoki Miyamoto, Yuya Oguro, 2013, Bioorganic & medicinal chemistry.

Structure-Based Approach for the Discovery of Pyrrolo[3,2-d]pyrimidine-Based EGFR T790M/L858R Mutant Inhibitors.

Yoshikazu Ohta, Tomoyasu Ishikawa, Terufumi Takagi, 2013, ACS medicinal chemistry letters.

Identification of Novel, Potent, and Orally Available GCN2 Inhibitors with Type I Half Binding Mode.

M. Klein, R. Tjhen, Biching Sang, 2019, ACS medicinal chemistry letters.

Constrained Peptides in Drug Discovery and Development

K. Masuya, P. Reid, D. R. Cary, 2017 .

Extended Solution-phase Peptide Synthesis Strategy Using Isostearyl-Mixed Anhydride Coupling and a New C-Terminal Silyl Ester-Protecting Group for N-Methylated Cyclic Peptide Production

K. Masuya, M. Yoshino, D. R. Cary, 2021, Organic Process Research & Development.

Macrocyclic Peptides as a Novel Class of NNMT Inhibitors: A SAR Study Aimed at Inhibitory Activity in the Cell.

Masataka Fumoto, Shiho Yamamoto, Shota Uehara, 2021, ACS medicinal chemistry letters.