Skip to content
5,7,8-trihydroxyflavone

Structure via PubChem · Public domain (PubChem)

EntityQ15425306· pop 7· linked from 407 articles

5,7,8-trihydroxyflavone

Sign in to save

Also known as 2-Phenyl-5,7,8-trihydroxy-4H-1-benzopyran-4-one, Norwogonin

Norwogonin, also known as 5,7,8-trihydroxyflavone (5,7,8-THF), is a flavone, a naturally occurring flavonoid-like chemical compound which is found in Scutellaria baicalensis (Baikal skullcap). It has been found to act as an agonist of the TrkB, the main signaling receptor of brain-derived neurotrophic factor (BDNF), and appears to possess roughly the same activity in this regard to that of the closely related but more well-known tropoflavin (7,8-DHF).

Chemical data

Formula
C15H10O5
Molecular weight
270.24 g/mol
IUPAC name
5,7,8-trihydroxy-2-phenylchromen-4-one
SMILES
C1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)O
InChIKey
ZFKKRRMUPBBYRS-UHFFFAOYSA-N
XLogP
2.7
Polar surface area
87 Ų
H-bond donors
3
H-bond acceptors
5
Formal charge
0

via PubChem

Drug data · ChEMBL

Molecule type
Small molecule

via ChEMBL · EBI

Wikidata facts

Subclass of
flavone
Mass
270.052823
Show 4 more facts
canonical SMILES
C1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)O
chemical formula
C₁₅H₁₀O₅
Commons category
Norwogonin
Sources (2)

via Wikidata · CC0

~1 min read

Encyclopedic overview

2 sections
Contents
  • See also
  • References

Norwogonin, also known as 5,7,8-trihydroxyflavone (5,7,8-THF), is a flavone, a naturally occurring flavonoid-like chemical compound which is found in Scutellaria baicalensis (Baikal skullcap). It has been found to act as an agonist of the TrkB, the main signaling receptor of brain-derived neurotrophic factor (BDNF), and appears to possess roughly the same activity in this regard to that of the closely related but more well-known tropoflavin (7,8-DHF).

== See also == Tropomyosin receptor kinase B § Agonists

Excerpted from Wikipedia’s “5,7,8-trihydroxyflavone” article, available under the CC BY-SA 4.0 licence.

Available in 6 languages

via Wikidata sitelinks · CC0