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pancreatic cancer cells

Targeting ASCT2-Mediated Glutamine Metabolism Inhibits Proliferation and Promotes Apoptosis of Pancreatic Cancer Cell

[Bioscience Reports] Scientists showed that alanine serine cysteine‑preferring transporter 2 (ASCT2) expression was significantly higher in pancreatic cancer than in normal pancreatic duct cells and pancreas.

A Two-Phase Approach to Fusicoccane Synthesis to Uncover a Compound That Reduces Tumourigenesis in Pancreatic Cancer Cells

[Angewandte Chemie-International Edition] Scientists generated 15 g of the tricyclic intermediate in 8 steps from ( R )-limonene and 720 mg of the penultimate bioactive intermediate in a protecting-group-free manner.

A Novel Chemo-Phenotypic Method Identifies Mixtures of Salpn, Vitamin D3, and Pesticides Involved in the Development of Colorectal and Pancreatic Cancer

[Ecotoxicology and Environmental Safety] Researchers described a novel computational method for characterizing toxicity, associated biological perturbations and disease outcome, called the Chemo-Phenotypic Based Toxicity Measurement. The method was validated in the in vitro, in vivo and organoid models.

A Comparison of 64Cu-Labeled Bi-terminally PEGylated A20FMDV2 Peptides Targeting Integrin ανβ6

[Oncotarget] Researchers described the radiolabeling, in vitro and in vivo evaluation of a bi-terminally PEGylated A20FMDV2 conjugated with DOTA or PCTA for 64Cu radiolabeling.

A Two-Phase Approach to Fusicoccane Synthesis to Uncover a Compound That Reduces Tumourigenesis in Pancreatic Cancer Cells

[Angewandte Chemie-International Edition] Scientists generated 15 g of the tricyclic intermediate in 8 steps from ( R )-limonene and 720 mg of the penultimate bioactive intermediate in a protecting-group-free manner.

A Novel Chemo-Phenotypic Method Identifies Mixtures of Salpn, Vitamin D3, and Pesticides Involved in the Development of Colorectal and Pancreatic Cancer

[Ecotoxicology and Environmental Safety] Researchers described a novel computational method for characterizing toxicity, associated biological perturbations and disease outcome, called the Chemo-Phenotypic Based Toxicity Measurement. The method was validated in the in vitro, in vivo and organoid models.

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