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Nobuo Shimma

Researcher at Hoffmann-La Roche

Publications -  92
Citations -  3268

Nobuo Shimma is an academic researcher from Hoffmann-La Roche. The author has contributed to research in topics: Alkyl & Capecitabine. The author has an hindex of 24, co-authored 92 publications receiving 3160 citations. Previous affiliations of Nobuo Shimma include Chugai Pharmaceutical Co..

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Journal ArticleDOI

Hispidospermidin, a novel phospholipase C inhibitor produced by Chaetosphaeronema hispidulum (Cda) Moesz NR 7127. II. Isolation, characterization and structural elucidation.

TL;DR: Hispidospermidin is a novel phospholipase C inhibitor produced by Chaetosphaeronema hispidulum (Cda) Moesz NR 7127 that has been elucidated as a cage compound with a trimethylspermidine side chain based on various NMR studies, including 1H-1H COSY, HOHAHA, HMBC, COLOC and long range J C-H resolved 2D spectroscopy.
Patent

3-[4-(4-cyanophenyl)thiazol-2-y)]-1-(1h-1,2,4-triazol-1-yl)-butan-2-ol derivatives having antifungal activity

TL;DR: Azole derivatives of formula (I) and the salts thereof can be used in the production of medicaments for treating fungal infections and mycoses as discussed by the authors, and they are a pharmaceutically acceptable anion.
Journal ArticleDOI

Cassette dosing approach and quantitative structure-pharmacokinetic relationship study of antifungal N-myristoyltransferase inhibitors.

TL;DR: The QSPKR model obtained is predictive and simple, and would give a direction for designing new Nmt inhibitors having good PK profiles, and the number of rotational bonds (Rotlbonds).
Journal ArticleDOI

Penitricin, a new class of antibiotic produced by Penicillium aculeatum. III. Structural confirmation by chemical synthesis and biological activity.

TL;DR: A novel antibiotic, penitricin showing anti-Gram-negative activity, has been isolated from the culture filtrate of Penicillium aculeatum and its structure was determined as hydroxymethylcyclopropenone by chemical synthesis from propargyl alcohol.
Journal ArticleDOI

3D-QSAR study of antifungal N-myristoyltransferase inhibitors by comparative molecular surface analysis

TL;DR: The 3D-QSAR model has given additional information about the binding of a benzofuran inhibitor to Nmt and the resulting best model is significantly more predictive than the one with all chemical descriptors.