Page last updated: 2024-08-23

staurosporine and 2-carboxyarabinitol 1-phosphate

staurosporine has been researched along with 2-carboxyarabinitol 1-phosphate in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's3 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ali, SF; Aziz, G; Hansen, TV; Paulsen, RE; Rongved, P; Strand, OA1
Botham, RC; Dirikolu, L; Fan, TM; Hergenrother, PJ; Roth, HS; Schmid, SC1
Bao, G; Du, B; Gong, P; Li, W; Lv, J; Ma, J; Wang, L; Xu, B; Zhai, X1

Other Studies

3 other study(ies) available for staurosporine and 2-carboxyarabinitol 1-phosphate

ArticleYear
Synthesis and initial in vitro biological evaluation of two new zinc-chelating compounds: comparison with TPEN and PAC-1.
    Bioorganic & medicinal chemistry, 2013, Sep-01, Volume: 21, Issue:17

    Topics: Amines; Animals; Apoptosis; Caspase 3; Caspase Inhibitors; Chelating Agents; Ethylenediamines; Hydrazones; PC12 Cells; Picolinic Acids; Piperazines; Pyridoxine; Rats; Reactive Oxygen Species; Zinc; Zinc Sulfate

2013
Removal of Metabolic Liabilities Enables Development of Derivatives of Procaspase-Activating Compound 1 (PAC-1) with Improved Pharmacokinetics.
    Journal of medicinal chemistry, 2015, May-14, Volume: 58, Issue:9

    Topics: Animals; Antineoplastic Agents; Apoptosis; Area Under Curve; Cell Line, Tumor; Dogs; Drug Screening Assays, Antitumor; Half-Life; Humans; Hydrazones; Mice; Microsomes, Liver; Piperazines; Rats; Small Molecule Libraries; Structure-Activity Relationship

2015
Design, synthesis, biological evaluation and preliminary mechanism study of novel benzothiazole derivatives bearing indole-based moiety as potent antitumor agents.
    European journal of medicinal chemistry, 2015, Volume: 96

    Topics: Antineoplastic Agents; Benzothiazoles; Cell Line, Tumor; Cell Proliferation; Dose-Response Relationship, Drug; Drug Design; Drug Screening Assays, Antitumor; Humans; Indoles; Models, Molecular; Molecular Structure; Quantitative Structure-Activity Relationship

2015