Page last updated: 2024-09-05

phenserine and physovenine

phenserine has been researched along with physovenine in 4 studies

Compound Research Comparison

Studies
(phenserine)
Trials
(phenserine)
Recent Studies (post-2010)
(phenserine)
Studies
(physovenine)
Trials
(physovenine)
Recent Studies (post-2010) (physovenine)
886391407

Protein Interaction Comparison

ProteinTaxonomyphenserine (IC50)physovenine (IC50)
CholinesteraseHomo sapiens (human)0.0067
AcetylcholinesteraseHomo sapiens (human)0.0155

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (25.00)18.2507
2000's1 (25.00)29.6817
2010's1 (25.00)24.3611
2020's1 (25.00)2.80

Authors

AuthorsStudies
Chaudhaery, SS; Nath, C; Nazir, A; Roy, KK; Sammi, SR; Saxena, AK; Saxena, G; Shakya, N1
Li, X; Wang, S; Wang, Y; Wang, Z; Zhang, H1
Brossi, A; Greig, NH; Ingram, DK; Pei, XF; Soncrant, TT1
Barak, D; Greig, NH; Ordentlich, A; Shafferman, A; Stein, D; Yu, QS1

Reviews

2 review(s) available for phenserine and physovenine

ArticleYear
Recent advance on carbamate-based cholinesterase inhibitors as potential multifunctional agents against Alzheimer's disease.
    European journal of medicinal chemistry, 2022, Oct-05, Volume: 240

    Topics: Aged; Alzheimer Disease; Carbamates; Cholinesterase Inhibitors; Humans; Ligands

2022
Phenserine and ring C hetero-analogues: drug candidates for the treatment of Alzheimer's disease.
    Medicinal research reviews, 1995, Volume: 15, Issue:1

    Topics: Alzheimer Disease; Animals; Cholinesterase Inhibitors; Humans; Physostigmine; Rats; Structure-Activity Relationship

1995

Other Studies

2 other study(ies) available for phenserine and physovenine

ArticleYear
Novel carbamates as orally active acetylcholinesterase inhibitors found to improve scopolamine-induced cognition impairment: pharmacophore-based virtual screening, synthesis, and pharmacology.
    Journal of medicinal chemistry, 2010, Sep-09, Volume: 53, Issue:17

    Topics: Acetylcholinesterase; Administration, Oral; Animals; Avoidance Learning; Caenorhabditis elegans; Carbamates; Catalytic Domain; Cholinesterase Inhibitors; Databases, Factual; Hydrogen Bonding; Hydrophobic and Hydrophilic Interactions; Male; Mice; Models, Molecular; Nootropic Agents; Quantitative Structure-Activity Relationship; Scopolamine

2010
Accommodation of physostigmine and its analogues by acetylcholinesterase is dominated by hydrophobic interactions.
    The Biochemical journal, 2009, Jan-01, Volume: 417, Issue:1

    Topics: Acetylcholinesterase; Binding Sites; Catalysis; Cholinesterase Inhibitors; Humans; Hydrophobic and Hydrophilic Interactions; Kinetics; Models, Molecular; Molecular Structure; Mutation; Phenylcarbamates; Physostigmine; Protein Binding; Pyridostigmine Bromide; Rivastigmine; Structure-Activity Relationship

2009