Pages that link to "Q48420847"
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The following pages link to Aliphatic propargylamines: potent, selective, irreversible monoamine oxidase B inhibitors (Q48420847):
Displaying 28 items.
- Symptomatic and neuroprotective properties of the aliphatic propargylamines (Q33828747) (← links)
- Aliphatic propargylamines as symptomatic and neuroprotective treatments for neurodegenerative diseases (Q34802137) (← links)
- Neuroprotection by propargylamines in Parkinson's disease: suppression of apoptosis and induction of prosurvival genes (Q34802158) (← links)
- Direct addition of alkynes to imines and related C=N electrophiles: A convenient access to propargylamines (Q36626654) (← links)
- Future of neuroprotection in Parkinson's disease (Q40693116) (← links)
- Relevance of benzyloxy group in 2-indolyl methylamines in the selective MAO-B inhibition (Q42039544) (← links)
- Effect of the ortho-hydroxy group of salicylaldehyde in the A3 coupling reaction: A metal-catalyst-free synthesis of propargylamine (Q42293322) (← links)
- Amine oxidases and their inhibitors: what can they tell us about neuroprotection and the development of drugs for neuropsychiatric disorders? (Q42399167) (← links)
- Chemoselective amination of propargylic C(sp³)-H bonds by cobalt(II)-based metalloradical catalysis (Q42764343) (← links)
- Effect of adding selegeline to levodopa in early, mild Parkinson's disease. Selegeline may be toxic in presence of increased dopamine concentrations (Q43187396) (← links)
- Formation of formaldehyde from adrenaline in vivo; a potential risk factor for stress-related angiopathy (Q43486869) (← links)
- Synthesis of N-propargylphenelzine and analogues as neuroprotective agents (Q43759907) (← links)
- Three‐Component Enantioselective Synthesis of Propargylamines through Zr‐Catalyzed Additions of Alkyl Zinc Reagents to Alkynylimines (Q44591982) (← links)
- N-Propargylamine protects SH-SY5Y cells from apoptosis induced by an endogenous neurotoxin, N-methyl(R)salsolinol, through stabilization of mitochondrial membrane and induction of anti-apoptotic Bcl-2. (Q46448361) (← links)
- N-(6-18F-fluorohexyl)-N-methylpropargylamine: a fluorine-18-labeled monoamine oxidase B inhibitor for potential use in PET studies (Q48252695) (← links)
- Aliphatic N-Methylpropargylamines: Monoamine Oxidase-B Inhibitors and Antiapoptotic Drugs (Q48609486) (← links)
- An Arylation Strategy to Propargylamines: Catalytic Asymmetric Friedel-Crafts-type Arylation Reactions of C-Alkynyl Imines (Q48954848) (← links)
- Immunohistochemical evidence of neuroprotection by R(-)-deprenyl and N-(2-hexyl)-N-methylpropargylamine on DSP-4-induced degeneration of rat brain noradrenergic axons and terminals (Q49116462) (← links)
- Prolongation of life in an experimental model of aging in Drosophila melanogaster. (Q52568284) (← links)
- Lanthanide-Catalyzed Reversible Alkynyl Exchange by Carbon-Carbon Single-Bond Cleavage Assisted by a Secondary Amino Group. (Q52855246) (← links)
- Highly Stereoselective Synthesis of Stereochemically Defined Polyhydroxylated Propargylamines by Alkynylation ofN-Benzylimines Derived from (R)-Glyceraldehyde (Q63344018) (← links)
- Some new mechanisms underlying the actions of (-)-deprenyl: possible relevance to neurodegeneration (Q70959414) (← links)
- Inhibition of MAO-B by (-)-deprenyl alters dopamine metabolism in the macaque (Macaca facicularis) brain (Q71492555) (← links)
- Enantioselective gas chromatographic assay of 2-alkylamines using N-(trifluoroacetyl)prolyl derivatives and a chiral capillary column (Q73134115) (← links)
- Development of N-[3-(2',4'-dichlorophenoxy)-2-18F-fluoropropyl]-N-methylpropargylamine (18F-fluoroclorgyline) as a potential PET radiotracer for monoamine oxidase-A (Q73247339) (← links)
- Behavioral and biochemical studies of dichloromethane fraction from the Areca catechu nut (Q73363228) (← links)
- Nanofibrils of a CuII-Thiophenyltriazine-Based Porous Polymer: A Diverse Heterogeneous Nanocatalyst (Q92760679) (← links)
- In Situ Immobilized Silver Nanoparticles on Rubia tinctorum Extract-Coated Ultrasmall Iron Oxide Nanoparticles: An Efficient Nanocatalyst with Magnetic Recyclability for Synthesis of Propargylamines by A3 Coupling Reaction (Q93190633) (← links)