scispace - formally typeset
T

Takashi Tsukamoto

Researcher at Johns Hopkins University

Publications -  91
Citations -  4465

Takashi Tsukamoto is an academic researcher from Johns Hopkins University. The author has contributed to research in topics: Glutamate carboxypeptidase II & Glutaminase. The author has an hindex of 29, co-authored 78 publications receiving 3802 citations. Previous affiliations of Takashi Tsukamoto include Johns Hopkins University School of Medicine & Chiba University.

Papers
More filters
Journal ArticleDOI

Design, synthesis, and pharmacological evaluation of bis-2-(5-phenylacetamido-1,2,4-thiadiazol-2-yl)ethyl sulfide 3 (BPTES) analogs as glutaminase inhibitors.

TL;DR: In an attempt to identify more potent GLS inhibitors with improved drug-like molecular properties, a series of BPTES analogs were synthesized and evaluated and revealed that some truncated analogs retained the potency of B PTES, presenting an opportunity to improve its aqueous solubility.
Journal ArticleDOI

Synthesis and biological evaluation of D-amino acid oxidase inhibitors.

TL;DR: Oral administration of CBIO in conjunction with d-serine enhanced the plasma and brain levels of d-Serine in rats compared to the oral administration of d -serine alone.
Journal ArticleDOI

Inhibition of glutaminase selectively suppresses the growth of primary acute myeloid leukemia cells with IDH mutations

TL;DR: This study lays the groundwork for strategies to target a specific subtype of AML metabolically with IDH mutations with a unique reprogramming of intermediary metabolism that culminates in glutamine dependency of cancer cells for survival.
Journal ArticleDOI

High-affinity near-infrared fluorescent small-molecule contrast agents for in vivo imaging of prostate-specific membrane antigen.

TL;DR: Nearly complete preclinical development of an optically based small-molecule contrast agent for image-guided surgery is described and sensitive and specific in vitro imaging of endogenous and ectopically expressed PSMA in human cells and in vivo imaging of xenograft tumors is demonstrated.
Journal ArticleDOI

Synthesis and biological evaluation of thiol-based inhibitors of glutamate carboxypeptidase II: discovery of an orally active GCP II inhibitor.

TL;DR: The most potent thiol-based inhibitor, 2-(3-mercaptopropyl)pentanedioic acid (IC(50) = 90 nM), was found to be orally bioavailable in rats and exhibited efficacy in an animal model of neuropathic pain following oral administration.