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По вашему запросу найдено документов: 401797

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Biofunctional chemistry and reactivity of biogenic acrolein for cancer diagnosis and therapy

Pradipta A.R., Tanaka K.

Acrolein holds excellent potential as a biomarker in various oxidative stress-related diseases

Targeted 1,3-dipolar cycloaddition with acrolein for cancer prodrug activation

Pradipta A.R., Ahmadi P., Terashima K., Muguruma K., Fujii M., Ichino T., Maeda S., Tanaka K.

significantly affect healthy cells. Prodrug therapy provides an alternative approach using a less cytotoxic form

Application of Acrolein Imines to Organic Synthesis, Biofunctional Studies, and Clinical Practice

Pradipta A.R., Tanaka K.

N-alkyl unsaturated imines derived from acrolein, a toxin produced during oxidative stress

In Vivo Gold Complex Catalysis within Live Mice

Tsubokura K., Vong K., Pradipta A., Ogura A., Urano S., Tahara T., Nozaki S., Onoe H., Nakao Y., Sibgatullina R., Kurbangalieva A., Watanabe Y., Tanaka K.

© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, WeinheimMetal complex catalysis within biological systems

Disease-associated acrolein: A possible diagnostic and therapeutic substrate for in vivo synthetic chemistry

Muguruma K., Pradipta A.R., Ode Y., Terashima K., Michiba H., Fujii M., Tanaka K.

© 2020 Elsevier Ltd Acrolein, a highly reactive α,β-unsaturated aldehyde, is a compound to which

Unexplored reactivity of N-alkyl unsaturated imines: A simple procedure for producing optically active 1,3-diamines via a stereocontrolled formal [4+2] and [4+2+2] iminocycloaddition

Pradipta A., Tanaka K.

imines derived from substituted aldehydes, a chiral aminoalcohol, and paraformaldehyde to produce

Enantioselective synthesis of cyclic and linear diamines by imine cycloadditions

Chang T.C., Pradipta A.R., Tanaka K.

derivatives in excellent yields. Under a similar condition, in the presence of formaldehyde, the [4 + 2

Microfluidic Mixing of Polyamine with Acrolein Enables the Detection of the [4+4] Polymerization of Intermediary Unsaturated Imines: The Properties of a Cytotoxic 1,5-Diazacyclooctane Hydrogel

Pradipta A., Tsutsui A., Ogura A., Hanashima S., Yamaguchi Y., Kurbangalieva A., Tanaka K.

The [4+4] polymerization of an unsaturated imine, generated from the condensation of a polyamine

Unexplored reactivity of N-alkyl unsaturated imines: A simple procedure for producing optically active 1,3-diamines via a stereocontrolled formal [4+2] and [4+2+2] iminocycloaddition

Pradipta A., Tanaka K.

imines derived from substituted aldehydes, a chiral aminoalcohol, and paraformaldehyde to produce

Expanding the Applicability of the Metal Labeling of Biomolecules by the RIKEN Click Reaction: A Case Study with Gallium-68 Positron Emission Tomography

Nakamoto Y., Pradipta A., Mukai H., Zouda M., Watanabe Y., Kurbangalieva A., Ahmadi P., Manabe Y., Fukase K., Tanaka K.

© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Radiolabeled biomolecules with short half

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