Alkaloids indolizidine 235B', quinolizidine 1-epi-207I, and the tricyclic 205B are potent and selective noncompetitive inhibitors of nicotinic acetylcholine receptors.

Alkaloids indolizidine 235B', quinolizidine 1-epi-207I, and the tricyclic 205B are potent and selective noncompetitive inhibitors of nicotinic acetylcholine receptors.

Item
http://www.wikidata.org/entity/Q34333976
First-Principles Determination of Molecular Conformations of Indolizidine (-)-235B' in SolutionIndolizidine (-)-235B' and related structural analogs: discovery of nicotinic receptor antagonists that inhibit nicotine-evoked [3H]dopamine releaseTotal synthesis of alkaloid 205B.Flexible synthetic routes to poison-frog alkaloids of the 5,8-disubstituted indolizidine-class I: synthesis of common lactam chiral building blocks and application to the synthesis of (-)-203A, (-)-205A, and (-)-219F.Flexible synthesis of poison-frog alkaloids of the 5,8-disubstituted indolizidine-class. II: Synthesis of (-)-209B, (-)-231C, (-)-233D, (-)-235B", (-)-221I, and an epimer of 193E and pharmacological effects at neuronal nicotinic acetylcholine receptSynthesis of alkaloid (-)-205B via stereoselective reductive cross-coupling and intramolecular [3+2] cycloaddition.Facile synthesis of two diastereomeric indolizidines corresponding to the postulated structure of alkaloid 5,9E-259B from a Bufonid toad (Melanophryniscus)Efficient enantio- and diastereodivergent synthesis of poison-frog alkaloids 251O and trans-223B.Asymmetric total synthesis of alkaloids 223A and 6-epi-223ACyclic enaminones. Part II: applications as versatile intermediates in alkaloid synthesis.A two-directional approach to pyrrolizidines: total syntheses and biological evaluation of alkaloid cis-223B and (±)-xenovenine.Non-competitive Inhibition of Nicotinic Acetylcholine Receptors by Ladybird Beetle Alkaloids.Metallacycle-Mediated Cross-Coupling in Natural Product Synthesis.Concise total synthesis of the frog alkaloid (-)-205B.
P2860

Alkaloids indolizidine 235B', quinolizidine 1-epi-207I, and the tricyclic 205B are potent and selective noncompetitive inhibitors of nicotinic acetylcholine receptors.

Item
http://www.wikidata.org/entity/Q34333976
description
2004 nî lūn-bûn
@nan
2004 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Alkaloids indolizidine 235B', ...... tinic acetylcholine receptors.
@ast
Alkaloids indolizidine 235B', ...... tinic acetylcholine receptors.
@en
Alkaloids indolizidine 235B', ...... tinic acetylcholine receptors.
@nl
type
label
Alkaloids indolizidine 235B', ...... tinic acetylcholine receptors.
@ast
Alkaloids indolizidine 235B', ...... tinic acetylcholine receptors.
@en
Alkaloids indolizidine 235B', ...... tinic acetylcholine receptors.
@nl
prefLabel
Alkaloids indolizidine 235B', ...... tinic acetylcholine receptors.
@ast
Alkaloids indolizidine 235B', ...... tinic acetylcholine receptors.
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Alkaloids indolizidine 235B', ...... tinic acetylcholine receptors.
@nl
P1433
P1476
P2093
P304
P31
P356
P433
P478
P577
P5875
P698
P356
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Alkaloids indolizidine 235B', ...... tinic acetylcholine receptors.
@en
P2093
P304
P31
P356
P433
P478
P577
P5875
P698