Compounds > 2-oxindole
Page last updated: 2024-08-24

2-oxindole and urea

2-oxindole has been researched along with urea in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (25.00)18.2507
2000's0 (0.00)29.6817
2010's3 (75.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Hull-Campbell, NE; Kent, LL; Lau, T; Nori, M; Thompson, SA; Wu, JC1
Chang, CN; Chen, CH; Chen, GS; Chen, YC; Chern, JW; Chou, NT; Chou, SH; Hseu, TH; Hsu, HC; Hu, TL; Huang, CH; Hwang, CS; Khanwelkar, RR; Ko, CH; Lee, O; Lin, HC; Lin, MW; Liu, CP; Shih, YC; Tsai, YJ; Tseng, HW; Tu, CM; Wang, HC; Wang, LM; Yu, CW1
Chang, PT; Chen, GS; Chern, JW; Jagtap, AD; Liu, CP; Liu, JR; Tseng, HW; Wang, HC1
Abdel-Aziz, HA; Alsherbiny, MA; Aly, MH; Eldehna, WM; Fares, M; Ghabbour, HA; Ibrahim, HS1

Other Studies

4 other study(ies) available for 2-oxindole and urea

ArticleYear
Characterization of novel inhibitors of cyclin-dependent kinases.
    Biochemical and biophysical research communications, 1999, Jul-14, Volume: 260, Issue:3

    Topics: Adenosine Triphosphate; Antineoplastic Agents; Benzoic Acid; Blotting, Western; Breast Neoplasms; Cell Division; Cyclin D1; Cyclin-Dependent Kinase 4; Cyclin-Dependent Kinases; Drug Screening Assays, Antitumor; Enzyme Inhibitors; Humans; Indoles; Inhibitory Concentration 50; Kinetics; Oxindoles; Proto-Oncogene Proteins; Retinoblastoma Protein; Substrate Specificity; Tumor Cells, Cultured; Urea

1999
Synthesis and structure-activity relationship of 6-arylureido-3-pyrrol-2-ylmethylideneindolin-2-one derivatives as potent receptor tyrosine kinase inhibitors.
    Bioorganic & medicinal chemistry, 2010, Jul-01, Volume: 18, Issue:13

    Topics: Animals; Aurora Kinases; Binding Sites; Cell Line, Tumor; Computer Simulation; Drug Screening Assays, Antitumor; ErbB Receptors; Humans; Indoles; Leukemia, Myeloid; Mice; Oxindoles; Protein Kinase Inhibitors; Protein Serine-Threonine Kinases; Pyrroles; Receptors, Platelet-Derived Growth Factor; Structure-Activity Relationship; Transplantation, Heterologous; Urea

2010
Bioisosteric replacement of an acylureido moiety attached to an indolin-2-one scaffold with a malonamido or a 2/4-pyridinoylamido moiety produces a selectively potent Aurora-B inhibitor.
    European journal of medicinal chemistry, 2014, Sep-12, Volume: 84

    Topics: Amides; Antineoplastic Agents; Apoptosis; Aurora Kinase B; Cell Line, Tumor; Cell Proliferation; Dihydropyridines; Dose-Response Relationship, Drug; Enzyme Inhibitors; Hep G2 Cells; Humans; Indoles; Malonates; Molecular Structure; Pyridones; Structure-Activity Relationship; Urea; Xenograft Model Antitumor Assays

2014
Synthesis and Cytotoxic Activity of Biphenylurea Derivatives Containing Indolin-2-one Moieties.
    Molecules (Basel, Switzerland), 2016, Jun-10, Volume: 21, Issue:6

    Topics: Antineoplastic Agents; Breast Neoplasms; Cell Proliferation; Doxorubicin; Drug Screening Assays, Antitumor; Female; Humans; Indoles; Male; MCF-7 Cells; Prostatic Neoplasms; Rhodamines; Structure-Activity Relationship; Urea

2016