(Q35447941)

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Identification of GABA A receptor modulators in Kadsura longipedunculata and assignment of absolute configurations by quantum-chemical ECD calculations

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21889177%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

Identification of GABA A receptor modulators in Kadsura longipedunculata and assignment of absolute configurations by quantum-chemical ECD calculations (English)

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21889177%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

Kadsura longepedunculata

object named as

Kadsura longipedunculata

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inferred from title

Martin Smieško

3

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12 February 2020

Matthias Hamburger

6

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Matthias Hamburger

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12 February 2020

Samad Nejad Ebrahimi

2

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Samad Nejad Ebrahimi

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12 February 2020

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Janine Zaugg

1

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12 February 2020

Igor Baburin

4

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12 February 2020

Steffen Hering

5

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12 February 2020

publication date

31 August 2011

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12 February 2020

1 reference

Europe PubMed Central

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12 February 2020

72

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12 February 2020

18

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12 February 2020

2385-2395

1 reference

Europe PubMed Central

PMC publication ID

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12 February 2020

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1 reference

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1 reference

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1 reference

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Analysis of Schisandra chinensis and Schisandra sphenanthera

1 reference

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International Union of Pharmacology. LXX. Subtypes of gamma-aminobutyric acid(A) receptors: classification on the basis of subunit composition, pharmacology, and function. Update

1 reference

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HPLC-based activity profiling approach for the discovery of GABAA receptor ligands using an automated two microelectrode voltage clamp assay on Xenopus oocytes

1 reference

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Pharmacology of Schisandra chinensis Bail.: an overview of Russian research and uses in medicine.

1 reference

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1 reference

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Patch clamp measurements on Xenopus laevis oocytes: currents through endogenous channels and implanted acetylcholine receptor and sodium channels

1 reference

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Identification and characterization of GABA(A) receptor modulatory diterpenes from Biota orientalis that decrease locomotor activity in mice.

1 reference

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26 September 2018

HPLC-based activity profiling of Angelica pubescens roots for new positive GABAA receptor modulators in Xenopus oocytes

1 reference

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A simple and sensitive HPLC method for the simultaneous determination of eight bioactive components and fingerprint analysis of Schisandra sphenanthera

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HPLC-based activity profiling: discovery of piperine as a positive GABA(A) receptor modulator targeting a benzodiazepine-independent binding site

1 reference

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1 reference

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Beyond polymaxenolide: Cembrane-africanane terpenoids from the hybrid soft coral Sinularia maxima x S. polydactyla

1 reference

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Sedative and hypnotic activities of the ethanol fraction from Fructus Schisandrae in mice and rats

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Dibenzo[a,c]cyclooctadiene lignans of the genus Schisandra: importance, isolation and determination

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1 reference

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Chemical constituents of two Chinese Magnoliaceae plants, Tsoongiodendron odorum and Manglietiastrum sinicum, and their inhibition of platelet aggregation

1 reference

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based on heuristic

inferred from PubMed ID database lookup

Stereochemical Investigations of Isochromenones and Isobenzofuranones Isolated fromLeptosphaeriasp. KTC 727

1 reference

https://pubmed.ncbi.nlm.nih.gov/21889177

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Argument on the correct Chinese name of genus Kadsura Kaempf.ex Juss]

1 reference

https://pubmed.ncbi.nlm.nih.gov/21889177

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

BI-32169, a Bicyclic 19-Peptide with Strong Glucagon Receptor Antagonist Activity fromStreptomycessp.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21889177

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based on heuristic

inferred from PubMed ID database lookup

[A study of the central pharmacological action of piperine and its derivatives]

1 reference

https://pubmed.ncbi.nlm.nih.gov/21889177

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The constituents of Kadsura japonica Dunal. I. The structures of three new lignans, acetyl-, angeloyl- and caproyl-binankadsurin A.

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.29.123

The constituents of Schizandra chinensis Baill. V. The structures of four new lignans, gomisin N, gomisin O, epigomisin O and gomisin E, and transformation of gomisin N to deangeloylgomisin B.

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.27.2695

Identifiers

10.1016/J.PHYTOCHEM.2011.08.014

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21889177%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21889177%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21889177%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

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