isomethyleugenol has been researched along with chiniofon in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (20.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 3 (60.00) | 24.3611 |
| 2020's | 1 (20.00) | 2.80 |
| Authors | Studies |
|---|---|
| Haradahira, T; Suzuki, K | 1 |
| Gengan, RM; Kumarsamy, C; Mohan, PS; Pandian, P | 1 |
| Beswick, P; Heightman, TD; Jadhav, A; Kawamura, A; King, ON; Klose, RJ; Li, XS; Maloney, DJ; Mott, BT; Ng, SS; Oppermann, U; Quinn, AM; Rai, G; Rose, NR; Sakurai, M; Schofield, CJ; Simeonov, A | 1 |
| Garneau-Tsodikova, S; Garzan, A; Mori, S; Tsodikov, OV | 1 |
| Denkhaus, L; Einsle, O; Fetzner, S; Gerhardt, S; Sartor, P | 1 |
5 other study(ies) available for isomethyleugenol and chiniofon
| Article | Year |
|---|---|
An improved synthesis of [11C]L-703,717 as a radioligand for the glycine site of the NMDA receptor.
Topics: Carbon Radioisotopes; Chromatography, High Pressure Liquid; Hydroxyquinolines; Methylation; Molecular Structure; Quinolones; Radiochemistry; Radioligand Assay; Receptors, Glycine; Receptors, N-Methyl-D-Aspartate; Sodium Hydroxide | 1999 |
Convenient and efficient microwave-assisted synthesis of a methyl derivative of the fused indoloquinoline alkaloid cryptosanguinolentine.
Topics: Alkaloids; Hydroxyquinolines; Indole Alkaloids; Indolequinones; Methylation; Microwaves; Quinaldines | 2010 |
Quantitative high-throughput screening identifies 8-hydroxyquinolines as cell-active histone demethylase inhibitors.
Topics: Biocatalysis; Dose-Response Relationship, Drug; Drug Evaluation, Preclinical; Enzyme Inhibitors; HeLa Cells; Histones; Humans; Hydroxyquinolines; Jumonji Domain-Containing Histone Demethylases; Lysine; Mass Spectrometry; Methylation; Molecular Structure | 2010 |
Deciphering Nature's Intricate Way of N,S-Dimethylating l-Cysteine: Sequential Action of Two Bifunctional Adenylation Domains.
Topics: Biosynthetic Pathways; Cysteine; Hydroxyquinolines; Methylation; Micromonosporaceae; Oligopeptides; Peptide Biosynthesis, Nucleic Acid-Independent; Peptide Synthases; Protein Domains | 2017 |
Structural basis of O-methylation of (2-heptyl-)1-hydroxyquinolin-4(1H)-one and related compounds by the heterocyclic toxin methyltransferase Rv0560c of Mycobacterium tuberculosis.
Topics: Amino Acid Sequence; Bacterial Proteins; Binding Sites; Biocatalysis; Catalytic Domain; Crystallography, X-Ray; Hydroxyquinolines; Methylation; Methyltransferases; Models, Chemical; Models, Molecular; Molecular Structure; Mutagenesis, Site-Directed; Mycobacterium tuberculosis; Protein Conformation; S-Adenosylmethionine; Sequence Homology, Amino Acid; Substrate Specificity | 2021 |