Page last updated: 2024-08-18

quinuclidines and 3-quinuclidinol

quinuclidines has been researched along with 3-quinuclidinol in 9 studies

Research

Studies (9)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (33.33)29.6817
2010's6 (66.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Allen, DD; Geldenhuys, WJ; Lockman, PR1
Barták, P; Bednár, P; Hlavác, J; Lemr, K; Sevcík, J; Stránský, Z; Stýskala, J; Wiedermannová, I1
Bosak, A; Orsulić, M; Primozic, I; Simeon-Rudolf, V; Tomić, S1
Kataoka, M; Nishimoto, Y; Nomoto, F; Sakoda, A; Shimizu, S; Uzura, A1
Isotani, K; Itoh, N; Kurokawa, J1
Isotani, K; Itoh, N; Kurokawa, J; Matsuda, M; Negishi, T; Nomoto, S; Suzuki, F1
Huang, L; Pan, J; Xu, GC; Xu, JH; Yu, HL; Zhang, WX1
Karthikraj, R; Murty, MR; Prabhakar, S; Raju, NP; Sridhar, L; Vairamani, M1
Degering, C; Hausmann, S; Leggewie, C; Schwaneberg, U; Spickermann, D1

Other Studies

9 other study(ies) available for quinuclidines and 3-quinuclidinol

ArticleYear
3-D-QSAR and docking studies on the neuronal choline transporter.
    Bioorganic & medicinal chemistry letters, 2010, Aug-15, Volume: 20, Issue:16

    Topics: Binding Sites; Blood-Brain Barrier; Computer Simulation; Membrane Transport Proteins; Models, Molecular; Neurons; Quantitative Structure-Activity Relationship; Quaternary Ammonium Compounds

2010
Capillary electrophoresis/mass spectrometry: a promising tool for the control of some physiologically hazardous compounds. I-derivatives of 3-quinuclidinol.
    Journal of mass spectrometry : JMS, 2002, Volume: 37, Issue:12

    Topics: Electrophoresis, Capillary; Fresh Water; Hallucinogens; Mass Spectrometry; Molecular Structure; Quinuclidines; Quinuclidinyl Benzilate; Sensitivity and Specificity; Water Pollutants

2002
Preparation of enantiomers of quinuclidin-3-Ol derivatives and their interactions with human cholinesterases.
    Chemico-biological interactions, 2005, Dec-15, Volume: 157-158

    Topics: Cholinesterase Inhibitors; Cholinesterases; Humans; Molecular Structure; Quinuclidines; Stereoisomerism

2005
Stereoselective synthesis of (R)-3-quinuclidinol through asymmetric reduction of 3-quinuclidinone with 3-quinuclidinone reductase of Rhodotorula rubra.
    Applied microbiology and biotechnology, 2009, Volume: 83, Issue:4

    Topics: Alcohol Oxidoreductases; Amino Acid Sequence; Base Sequence; Biotransformation; Cloning, Molecular; DNA, Fungal; Escherichia coli; Fungal Proteins; Gene Expression; Glucose 1-Dehydrogenase; Molecular Sequence Data; Quinuclidines; Rhodotorula; Sequence Analysis, DNA; Sequence Homology, Amino Acid; Stereoisomerism

2009
Production of (R)-3-quinuclidinol by E. coli biocatalysts possessing NADH-dependent 3-quinuclidinone reductase (QNR or bacC) from Microbacterium luteolum and Leifsonia alcohol dehydrogenase (LSADH).
    International journal of molecular sciences, 2012, Oct-19, Volume: 13, Issue:10

    Topics: Actinomycetales; Alcohol Dehydrogenase; Biocatalysis; Escherichia coli; Genetic Vectors; NADH, NADPH Oxidoreductases; Optical Rotation; Quinuclidines; Stereoisomerism; Time Factors

2012
Gene cloning and characterization of two NADH-dependent 3-quinuclidinone reductases from Microbacterium luteolum JCM 9174.
    Applied and environmental microbiology, 2013, Volume: 79, Issue:4

    Topics: Actinomycetales; Amino Acid Sequence; Cloning, Molecular; Coenzymes; DNA, Bacterial; Escherichia coli; Molecular Sequence Data; NAD; Oxidoreductases; Quinuclidines; Recombinant Fusion Proteins; Sequence Alignment; Sequence Analysis, DNA; Substrate Specificity

2013
Highly efficient synthesis of (R)-3-quinuclidinol in a space-time yield of 916 g L(-1) d(-1) using a new bacterial reductase ArQR.
    Organic letters, 2013, Oct-04, Volume: 15, Issue:19

    Topics: 3-Hydroxyacyl-CoA Dehydrogenase; Escherichia coli; Quinuclidines; Stereoisomerism

2013
p-Tolyl isocyanate derivatization for analysis of CWC-related polar degradation products by mass spectrometry.
    Analytical and bioanalytical chemistry, 2014, Volume: 406, Issue:21

    Topics: Chemical Warfare Agents; Ethanolamines; Gas Chromatography-Mass Spectrometry; Humans; Hydroxides; Isocyanates; Quinuclidines; Spectrometry, Mass, Electrospray Ionization; Static Electricity; Sulfhydryl Compounds

2014
Engineering of highly selective variants of Parvibaculum lavamentivorans alcohol dehydrogenase.
    Chembiochem : a European journal of chemical biology, 2014, Sep-22, Volume: 15, Issue:14

    Topics: Alcohol Dehydrogenase; Alphaproteobacteria; Catalytic Domain; Models, Molecular; Mutation; Oxidation-Reduction; Protein Engineering; Quinuclidines

2014