Search Results - "LEE, Mase"
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1
Comparative Metabolite Profiling of Wild and Cultivated Justicia procumbens L. Based on 1H-NMR Spectroscopy and HPLC-DAD Analysis
Published in Plants (Basel) (07-07-2020)“…Justicia procumbens L. is known across Korea, India, China, and Taiwan as a remedy against fever, cough, sore throat, and cirrhosis of ascites. J. procumbens…”
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2
The medicinal chemistry of 5-HT6 receptor ligands with a focus on arylsulfonyltryptamine analogs
Published in Current topics in medicinal chemistry (01-04-2010)“…Arylsulfonyl analogs of aminopyrimidines (e.g. Ro 04-6790; 2), aminopyridines (e.g. Ro 63-0563; 3), 1-phenylpiperazines (e.g. SB-271046; 4), and tryptamines…”
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3
Preparation of Novel Donepezil Long‐Acting Injectable, IVL3003, and its Pharmacokinetic Study via Subcutaneous Injection in Dogs and Monkeys
Published in Alzheimer's & dementia (01-12-2023)“…Background Donepezil is a selective oral acetylcholinesterase inhibitor to treat Alzheimer’s disease (AD). Most patients with AD need help with taking oral…”
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4
In Vitro Inhibitory Effect of Some Flavonoids on Rotavirus Infectivity
Published in Biological & pharmaceutical bulletin (01-09-2000)“…The inhibitory effects of some flavonoids on the infectivity of rotavirus, which predominantly causes sporadic diarrhea in infants and young children, were…”
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5
Development of a novel long-acting injectable, IVL4002 for modulation of multiple sclerosis: Pharmacokinetics and efficacy studies in an experimental autoimmune encephalomyelitis mouse model
Published in The Journal of immunology (1950) (01-05-2024)“…Multiple sclerosis (MS), a prevalent autoimmune disease and lacking a well-defined etiology and cures, drove the development of diverse disease-modifying…”
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6
A Phase I, Open-Label, Sequential, Single-Dose Clinical Trial to Evaluate the Pharmacokinetic, Pharmacodynamic, and Safety of IVL3001, a Finasteride-Based Novel Long-Acting Injection for Androgenetic Alopecia
Published in Advances in therapy (01-07-2024)“…Introduction Hair loss is driven by multiple factors, including genetics. Androgenetic alopecia (AGA) is a condition in which treatments necessitate prolonged…”
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7
Construction of three types of fused isoindoles via furan-pyrrole ring exchange reaction
Published in Tetrahedron (10-06-1996)“…The new synthetic route of three types of fused isoindoles using furan-pyrrole ring exchange reaction as the main synthetic strategy is presented…”
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8
Formulation and evaluation of an alternative triglyceride-free propofol microemulsion
Published in Archives of pharmacal research (01-09-2010)“…A new triglyceride-free propofol microemulsion for intravenous injection was formulated using nonionic surfactants, poloxamers and polyethylene glycol 660…”
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9
2-Substituted tryptamines: agents with selectivity for 5-HT(6) serotonin receptors
Published in Journal of medicinal chemistry (09-03-2000)“…Several 2-alkyl-5-methoxytryptamine analogues were designed and prepared as potential 5-HT(6) serotonin agonists. It was found that 5-HT(6) receptors…”
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10
N1-(Benzenesulfonyl)tryptamines as novel 5-HT6 antagonists
Published in Bioorganic & medicinal chemistry letters (01-10-2000)Get full text
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11
2-Substituted Tryptamines: Agents with Selectivity for 5-HT6 Serotonin Receptors
Published in Journal of medicinal chemistry (09-03-2000)“…Several 2-alkyl-5-methoxytryptamine analogues were designed and prepared as potential 5-HT6 serotonin agonists. It was found that 5-HT6 receptors accommodate…”
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12
N1-(Benzenesulfonyl)tryptamines as novel 5-HT6 antagonists
Published in Bioorganic & medicinal chemistry letters (16-10-2000)“…N-Benzenesulfonyl-5-methoxy-N,N-dimethyltryptamine (BS/5-OMe DMT; 5) was shown to bind at human 5-HT6 serotonin receptors with high affinity (Ki = 2.3 nM)…”
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13
1-(1-Naphthyl)piperazine as a novel template for 5-HT6 serotonin receptor ligands
Published in Bioorganic & medicinal chemistry letters (15-03-2005)“…4-Sulfonyl analogs of 1-(1-naphthyl)piperazine bind at human 5-HT6 receptors and represent a novel class of human 5-HT6 receptor ligands…”
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14
S(+)- and R(−) N-Methyl-1-(3,4-methylenedioxyphenyl)-2-aminopropane (MDMA) as discriminative stimuli: Effect of cocaine
Published in Pharmacology, biochemistry and behavior (01-11-2005)“…Racemic N-methyl-1-(3,4-methylenedioxyphenyl)-2-aminopropane (methylenedioxymethamphetamine, MDMA), a central stimulant and empathogenic agent, and cocaine are…”
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15
1-(1-Naphthyl)piperazine as a novel template for 5-HT 6 serotonin receptor ligands
Published in Bioorganic & medicinal chemistry letters (2005)“…4-Arylsulfone derivatives of 1-(1-naphthyl)piperazine represent a novel class of human 5-HT 6 serotonin receptor ligands. In particular, compounds such as 1f (…”
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16
3-(4-Aminobutyn-1-yl)pyridines: binding at α4β2 nicotinic cholinergic receptors
Published in Bioorganic & medicinal chemistry letters (2004)“…The binding of a series pyridylbutynylamines 6 was examined at α4β2 nACh receptors. Structural modifications, comparing 6 with pyridyl ethers 2, did not…”
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17
Quaternary ammonium 3-(aminoethoxy)pyridines as antinociceptive agents
Published in Bioorganic & medicinal chemistry letters (01-09-2003)“…Quaternization via N-methylation of the terminal amines of a series of 3-(dialkylaminoethoxy)pyridines resulted in analogues that displayed up to 50–60-fold…”
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18
Enantioselective Total Synthesis of cis-Trikentrin B
Published in Journal of organic chemistry (17-05-1996)“…Natural cis-trikentrin B was synthesized enantioselectively using, as key steps, an intramolecular Diels−Alder reaction of an allenic dienamide followed by…”
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19
6-(2-Phenylethyl)nicotine: A novel nicotinic cholinergic receptor ligand
Published in Bioorganic & medicinal chemistry letters (01-07-2005)“…Defying presumed structure–affinity relationships, nicotine analog 1b ( K i = 15 nM) was unexpectedly found to bind to α4β2 nACh receptors. Administered via an…”
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20
3-(4-Aminobutyn-1-yl)pyridines: binding at alpha 4 beta 2 nicotinic cholinergic receptors
Published in Bioorganic & medicinal chemistry letters (19-01-2004)“…The binding of a series pyridylbutynylamines 6 was examined at alpha4beta2 nACh receptors. Structural modifications, comparing 6 with pyridyl ethers 2, did not…”
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