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1-oxo-1,2,3,4-tetrahydroisoquinoline and indazoles

1-oxo-1,2,3,4-tetrahydroisoquinoline has been researched along with indazoles in 1 studies

*Indazoles: A group of heterocyclic aromatic organic compounds consisting of the fusion of BENZENE and PYRAZOLES. [MeSH]

*Indazoles: A group of heterocyclic aromatic organic compounds consisting of the fusion of BENZENE and PYRAZOLES. [MeSH]

Compound Research Comparison

Studies
(1-oxo-1,2,3,4-tetrahydroisoquinoline)
Trials
(1-oxo-1,2,3,4-tetrahydroisoquinoline)
Recent Studies (post-2010)
(1-oxo-1,2,3,4-tetrahydroisoquinoline)
Studies
(indazoles)
Trials
(indazoles)
Recent Studies (post-2010) (indazoles)
8055,6095503,265

Protein Interaction Comparison

ProteinTaxonomy1-oxo-1,2,3,4-tetrahydroisoquinoline (IC50)indazoles (IC50)
Chain A, Cell Division Protein Kinase 2Homo sapiens (human)185
Chain A, CELL DIVISION PROTEIN KINASE 2Homo sapiens (human)185
Chain A, Cell Division Protein Kinase 2Homo sapiens (human)185
Chain A, CELL DIVISION PROTEIN KINASE 2Homo sapiens (human)185
Chain A, CELL DIVISION PROTEIN KINASE 2Homo sapiens (human)185
Chain A, CELL DIVISION PROTEIN KINASE 2Homo sapiens (human)185
Chain A, CELL DIVISION PROTEIN KINASE 2Homo sapiens (human)185
Chain A, CELL DIVISION PROTEIN KINASE 2Homo sapiens (human)185
Chain A, CELL DIVISION PROTEIN KINASE 2Homo sapiens (human)185
Chain A, CELL DIVISION PROTEIN KINASE 2Homo sapiens (human)185
Chain A, CELL DIVISION PROTEIN KINASE 2Homo sapiens (human)185
Chain A, CELL DIVISION PROTEIN KINASE 2Homo sapiens (human)185
Chain A, CELL DIVISION PROTEIN KINASE 2Homo sapiens (human)185
Chain A, Cell Division Protein Kinase 2Homo sapiens (human)185

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Guo, WH; Huang, SS; Kong, LY; Li, XM; Yang, MH1

Other Studies

1 other study(ies) available for 1-oxo-1,2,3,4-tetrahydroisoquinoline and indazoles

ArticleYear
Three new alkaloids from the seeds of Nigella glandulifera.
    Journal of Asian natural products research, 2017, Volume: 19, Issue:1

    Topics: Alkaloids; Drugs, Chinese Herbal; Indazoles; Isoquinolines; Molecular Structure; Nigella; Nuclear Magnetic Resonance, Biomolecular; Phenylurea Compounds; Seeds

2017