Compounds > indole

indole and piperidine

indole has been researched along with piperidine in 4 studies

Research

Studies (4)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (50.00)	29.6817
2010's	1 (25.00)	24.3611
2020's	1 (25.00)	2.80

Authors

Authors	Studies
Bartoszyk, GD; Böttcher, H; Greiner, HE; Heinrich, T; Seyfried, CA; Van Amsterdam, C	1
Curillová, Z; Kutschy, P; McDonald, J; Mezencev, R; Mojzis, J; Pilátová, M; Salayová, A	1
Anderskewitz, R; Dollinger, H; Grundl, MA; Kriegl, JM; Martyres, D; Rast, G; Schmid, B; Seither, P; Tautermann, CS	1
Abe, H; Asawa, Y; Katsuragi, K; Makino, K; Nakamura, H; Nomura, M; Ogino, Y; Okazawa, M; Oyama, T; Sakamoto, Y; Sato, A; Shibasaki, Y; Takahashi, H; Tanuma, N; Tanuma, SI; Uchiumi, F; Yamazaki, H; Yoshimori, A	1

Other Studies

4 other study(ies) available for indole and piperidine

Article	Year
Indolebutylamines as selective 5-HT(1A) agonists. Journal of medicinal chemistry, 2004, Sep-09, Volume: 47, Issue:19 Topics: Animals; Biological Availability; Butylamines; Hippocampus; Humans; Indoles; Inhibitory Concentration 50; Male; Molecular Structure; Oxindoles; Piperidines; Pyridines; Rats; Receptor, Serotonin, 5-HT1A; Serotonin 5-HT1 Receptor Agonists; Structure-Activity Relationship; Substrate Specificity	2004
Anticancer properties of 2-piperidyl analogues of the natural indole phytoalexin 1-methoxyspirobrassinol. Chemotherapy, 2008, Volume: 54, Issue:5 Topics: Antineoplastic Agents; Biological Products; Cell Line, Tumor; Cell Proliferation; Drug Evaluation, Preclinical; Humans; Indoles; Molecular Structure; Piperidines; Spiro Compounds; Structure-Activity Relationship	2008
Rodent selectivity of piperidine-4-yl-1H-indoles, a series of CC chemokine receptor-3 (CCR3) antagonists: insights from a receptor model. Bioorganic & medicinal chemistry letters, 2015, Jan-15, Volume: 25, Issue:2 Topics: Animals; Humans; Indoles; Mice; Models, Molecular; Piperidines; Protein Structure, Secondary; Protein Structure, Tertiary; Rats; Receptors, CCR3; Species Specificity	2015
Structural Basis of Beneficial Design for Effective Nicotinamide Phosphoribosyltransferase Inhibitors. Molecules (Basel, Switzerland), 2020, Aug-10, Volume: 25, Issue:16 Topics: Binding Sites; Catalytic Domain; Drug Design; Enzyme Inhibitors; Humans; Indoles; Kinetics; Molecular Docking Simulation; Nicotinamide Phosphoribosyltransferase; Piperazine; Piperidines	2020