5,7-Dihydroxy-6-methoxyflavone, a benzodiazepine site ligand isolated from Scutellaria baicalensis Georgi, with selective antagonistic properties (Q28180798)

From Wikidata

Jump to navigation Jump to search

scientific article (publication date: July 2003)

Language	Label	Description	Also known as
English	5,7-Dihydroxy-6-methoxyflavone, a benzodiazepine site ligand isolated from Scutellaria baicalensis Georgi, with selective antagonistic properties	scientific article (publication date: July 2003)

Statements

scholarly article

0 references

5,7-Dihydroxy-6-methoxyflavone, a benzodiazepine site ligand isolated from Scutellaria baicalensis Georgi, with selective antagonistic properties (English)

0 references

2 references

ChEBI release 2020-05-28

Scutellaria baicalensis

1 reference

object named as

Hong Xue

7

0 references

author name string

Michael S Y Huen

1

0 references

Justin W C Leung

2

0 references

Wah Ng

3

0 references

W S Lui

4

0 references

Michelle N S Chan

5

0 references

J Tze-Fei Wong

6

0 references

language of work or name

0 references

publication date

July 2003

1 reference

16 September 2022

Biochemical Pharmacology

0 references

66

0 references

1

0 references

125-32

0 references

High affinity of the naturally-occurring biflavonoid, amentoflavon, to brain benzodiazepine receptors in vitro

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2803%2900233-8

7 January 2021

Chrysin (5,7-di-OH-flavone), a naturally-occurring ligand for benzodiazepine receptors, with anticonvulsant properties

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2803%2900233-8

7 January 2021

6-Bromoflavone, a high affinity ligand for the central benzodiazepine receptors is a member of a family of active flavonoids.

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2803%2900233-8

7 January 2021

6,3'-dibromoflavone and 6-nitro-3'-bromoflavone: new additions to the 6,3'-disubstituted flavone family of high-affinity ligands of the brain benzodiazepine binding site with agonistic properties

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2803%2900233-8

7 January 2021

6-Chloro-3'-nitroflavone is a potent ligand for the benzodiazepine binding site of the GABA(A) receptor devoid of intrinsic activity

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2803%2900233-8

7 January 2021

6-Methyl-3'-bromoflavone, a high-affinity ligand for the benzodiazepine binding site of the GABA(A) receptor with some antagonistic properties

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2803%2900233-8

7 January 2021

GABAergic modulation of benzodiazepine binding site sensitivity

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2803%2900233-8

7 January 2021

Flumazenil in drug overdose: randomized, placebo-controlled study to assess cost effectiveness.

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2803%2900233-8

7 January 2021

The use of flumazenil in the management of acute drug poisoning — a review

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2803%2900233-8

7 January 2021

Effects of the benzodiazepine receptor antagonist flumazenil in hepatic encephalopathy in humans.

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2803%2900233-8

7 January 2021

Antiviral Chinese medicinal herbs against respiratory syncytial virus

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2803%2900233-8

7 January 2021

Wogonin inhibits inducible prostaglandin E(2) production in macrophages

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2803%2900233-8

7 January 2021

Baicalin and baicalein, constituents of an important medicinal plant, inhibit intracellular Ca2+ elevation by reducing phospholipase C activity in C6 rat glioma cells.

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2803%2900233-8

7 January 2021

Interaction of flavones from the roots of Scutellaria baicalensis with the benzodiazepine site

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2803%2900233-8

7 January 2021

Anxiolytic effect of wogonin, a benzodiazepine receptor ligand isolated from Scutellaria baicalensis Georgi

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2803%2900233-8

7 January 2021

Effects of time of day and food deprivation on exploratory activity in the rat.

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2803%2900233-8

7 January 2021

Factor analysis of spatiotemporal and ethological measures in the murine elevated plus-maze test of anxiety

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2803%2900233-8

7 January 2021

Ethopharmacological analysis of rat behavior on the elevated plus-maze.

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2803%2900233-8

7 January 2021

Benzodiazepine antagonist Ro 15-1788: Neurological and behavioral effects

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2803%2900233-8

7 January 2021

Overview--flavonoids: a new family of benzodiazepine receptor ligands.

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2803%2900233-8

7 January 2021

GABA(A)-receptor ligands of flavonoid structure

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2803%2900233-8

7 January 2021

Gossypin-induced analgesia in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2803%2900233-8

7 January 2021

Benzodiazepine actions mediated by specific gamma-aminobutyric acid(A) receptor subtypes.

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2803%2900233-8

7 January 2021

Molecular and neuronal substrate for the selective attenuation of anxiety.

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2803%2900233-8

7 January 2021

Molecular targets for the myorelaxant action of diazepam.

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2803%2900233-8

7 January 2021

Mechanism of action of the hypnotic zolpidem in vivo

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2803%2900233-8

7 January 2021

Resolving differences in GABAA receptor mutant mouse studies.

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2803%2900233-8

7 January 2021

Detection of benzodiazepine receptor ligands in small libraries of flavone derivatives synthesized by solution phase combinatorial chemistry

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2803%2900233-8

7 January 2021

Structure-activity relationships and molecular modeling analysis of flavonoids binding to the benzodiazepine site of the rat brain GABA(A) receptor complex

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2803%2900233-8

7 January 2021

Molecular modeling and QSAR analysis of the interaction of flavone derivatives with the benzodiazepine binding site of the GABA(A) receptor complex

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2803%2900233-8

7 January 2021

3D-QSAR model of flavonoids binding at benzodiazepine site in GABAA receptors

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2803%2900233-8

7 January 2021

Identifiers

10.1016/S0006-2952(03)00233-8

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q28180798&oldid=2090705830"