pyrroles has been researched along with isoquinoline in 10 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (10.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 3 (30.00) | 29.6817 |
2010's | 6 (60.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Kelland, LR; Thurston, DE; Tsotinis, A; Vlachou, M | 1 |
Dewey, WL; Elzey, MJ; Javed, RR; Smith, FL | 1 |
MENZEL, R; SCHNEIDER, W | 1 |
Adams, DR; Bentley, JM; Benwell, KR; Bickerdike, MJ; Bodkin, CD; Cliffe, IA; Dourish, CT; George, AR; Kennett, GA; Knight, AR; Malcolm, CS; Mansell, HL; Misra, A; Quirk, K; Roffey, JR; Vickers, SP | 1 |
Aichholz, R; Feifel, R; Hawtin, S; Heng, R; Hiestand, P; Huppertz, C; Jahnke, W; Koch, G; Kroemer, M; Möbitz, H; Revesz, L; Scheufler, C; Schlapbach, A; Velcicky, J | 1 |
Fajardo, C; Fraile, A; González, G; Martín, MR; Martín-Castro, AM; Ruano, JL | 1 |
Huang, L; Jiang, H; Qi, C; Tang, X; Wu, W | 1 |
Chen, J; Liao, W; Xu, Q | 1 |
Manjappa, KB; Syu, JR; Yang, DY | 1 |
B Manjappa, K; Lin, JM; Yang, DY | 1 |
10 other study(ies) available for pyrroles and isoquinoline
Article | Year |
---|---|
An expeditious synthesis of cytotoxic pyrroloisoquinoline derivatives. Structure-activity comparative studies with isomeric pyrroloquinolines.
Topics: Female; Humans; Isomerism; Isoquinolines; Pyrroles; Structure-Activity Relationship; Tumor Cells, Cultured | 2002 |
The expression of a high level of morphine antinociceptive tolerance in mice involves both PKC and PKA.
Topics: Analgesics; Animals; Brain; Carbazoles; Cyclic AMP-Dependent Protein Kinases; Dose-Response Relationship, Drug; Drug Interactions; Drug Therapy, Combination; Drug Tolerance; Enzyme Inhibitors; Indoles; Injections, Intraventricular; Isoquinolines; Male; Maleimides; Mice; Morphine; Morphine Dependence; Pain; Protein Kinase C; Protein Serine-Threonine Kinases; Pyrroles | 2003 |
[2,1-a] isoquinoline].
Topics: Isoquinolines; Pyrroles; Quinolines | 1962 |
Pyrrolo(iso)quinoline derivatives as 5-HT(2C) receptor agonists.
Topics: Animals; Anti-Obesity Agents; Disease Models, Animal; Eating; Isoquinolines; Pyrroles; Quinolines; Radioligand Assay; Rats; Serotonin 5-HT2 Receptor Agonists; Serotonin Receptor Agonists | 2006 |
In vivo and in vitro SAR of tetracyclic MAPKAP-K2 (MK2) inhibitors. Part I.
Topics: Administration, Oral; Amino Acids; Animals; Binding Sites; Crystallography, X-Ray; Heterocyclic Compounds, 4 or More Rings; Humans; Intracellular Signaling Peptides and Proteins; Isoquinolines; Ketones; Lactams; Mice; Protein Kinase Inhibitors; Protein Serine-Threonine Kinases; Pyrroles; Structure-Activity Relationship; Tumor Necrosis Factor-alpha | 2010 |
Asymmetric synthesis of pyrrolo[2,1-a]isoquinoline derivatives by 1,3-dipolar cycloadditions of stabilized isoquinolinium N-ylides with sulfinyl dipolarophiles.
Topics: Isoquinolines; Nitrogen; Pyrroles; Quinolinium Compounds; Sulfoxides | 2011 |
An efficient synthesis of polysubstituted pyrroles via copper-catalyzed coupling of oxime acetates with dialkyl acetylenedicarboxylates under aerobic conditions.
Topics: Acetates; Acetylene; Carboxylic Acids; Catalysis; Copper; Isoquinolines; Oximes; Pyrroles | 2013 |
Metal-free intramolecular carbocyanation of alkenes: catalytic stereoselective construction of pyrrolo[2,1-a]isoquinolines with multiple substituents.
Topics: Alkenes; Catalysis; Crystallography, X-Ray; Cyclization; Isoquinolines; Models, Molecular; Nitriles; Pyrroles; Stereoisomerism | 2014 |
Visible-Light-Promoted and Yb(OTf)3-Catalyzed Constructions of Coumarin-Pyrrole-(Iso)quinoline-Fused Pentacycles: Synthesis of Lamellarin Core, Lamellarin D Trimethyl Ether, and Lamellarin H.
Topics: Catalysis; Coumarins; Cyclization; Ethers; Heterocyclic Compounds, 4 or More Rings; Isoquinolines; Light; Mesylates; Molecular Structure; Nitro Compounds; Organometallic Compounds; Pyrroles | 2016 |
Construction of Pentacyclic Lamellarin Skeleton via Grob Reaction: Application to Total Synthesis of Lamellarins H and D.
Topics: Coumarins; Heterocyclic Compounds, 4 or More Rings; Isoquinolines; Molecular Structure; Pyrroles; Stereoisomerism | 2017 |