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Makoto Sasaki

Researcher at Tohoku University

Publications -  319
Citations -  7275

Makoto Sasaki is an academic researcher from Tohoku University. The author has contributed to research in topics: Total synthesis & Ring (chemistry). The author has an hindex of 46, co-authored 303 publications receiving 6915 citations. Previous affiliations of Makoto Sasaki include Hokkaido University & Kyushu University.

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Transcellular transport of organic anions across a double-transfected Madin-Darby canine kidney II cell monolayer expressing both human organic anion-transporting polypeptide (OATP2/SLC21A6) and multidrug resistance-associated protein 2 (MRP2/ABCC2)

TL;DR: A double-transfected Madin-Darby canine kidney (MDCK II) cell monolayer is established, which expresses both OATP2 and MRP2 on basal and apical membranes, respectively, and may be used to analyze the hepatic vectorial transport of organic anions and to screen the transport profiles of new drug candidates.
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Identification of the Hepatic Efflux Transporters of Organic Anions Using Double-Transfected Madin-Darby Canine Kidney II Cells Expressing Human Organic Anion-Transporting Polypeptide 1B1 (OATP1B1)/Multidrug Resistance-Associated Protein 2, OATP1B1/Multidrug Resistance 1, and OATP1B1/Breast Cancer Resistance Protein

TL;DR: Two kinds of 3-hydroxy-3-methylglutaryl-CoA reductase inhibitors, CER and PRA, were also substrates of all these efflux transporters, and the rank order of the efflux clearance of PRA mediated by each transporter was the same as that of EG, whereas the contribution of MDR1 to theefflux of CER was relatively greater than for PRA.
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Development of a 3DOF mobile exoskeleton robot for human upper-limb motion assist

TL;DR: A mechanism and control method of a mobile exoskeleton robot for 3DOF upper-limb motion assist (shoulder vertical and horizontal flexion/extension, and elbow flexion-extension motion assist) and an obstacle avoidance algorithm is applied to prevent accidental collision between the user's upper- Limb and the robot frame is proposed.
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Total Synthesis of Gambierol

TL;DR: The first total synthesis of (-)-gambierol (1), a marine polycyclic ether toxin, has been achieved as discussed by the authors, which includes a convergent union of the ABC and EFGH ring fragments via a developed B-alkyl Suzuki-Miyaura cross-coupling strategy leading to the octacyclic polyether core 4 and a late-stage introduction of the sensitive triene side chain by use of Pd(PPh(3))(4)/CuCl/LiCl-promoted Stille coupling.