Basic Molecular Information

Basic Information

DICL ID
DICL_CP_0323534
PubChem CID
Molecular Formula
C16H12O5
Molecular Weight
284.267 g/mol
Synonyms/Alias
[acacetin; 480-44-4; Linarigenin; 57-Dihydroxy-4-methoxyflavone; Buddleoflavonol; Acacetine; 4-Methoxyapigenin; 57-Dihydroxy-2-(4-methoxyphenyl)-4H-chromen-4-one; Linarisenin; Apigenin 4-methyl ether;...
InChI Key
DANYIYRPLHHOCZ-UHFFFAOYSA-N
InChI
InChI=1S/C16H12O5/c1-20-11-4-2-9(3-5-11)14-8-13(19)16-12(18)6-10(17)7-15(16)21-14/h2-8,17-18H,1H3
IUPAC Name
57-dihydroxy-2-(4-methoxyphenyl)chromen-4-one
CAS Number
481-53-8

Structure Information

Chemical Structure Visualization

SMILES Notation
2D Molecular Drawing
Carbon (C)
Hydrogen (H)
Oxygen (O)
Nitrogen (N)
Sulfur (S)
SDF

33 35 0 0 0 0 0 0 0 0999 V2000
6.4686 -0.0479 -0.1918 C 0 0 0 0 0 0 0 0 0 0 0 0
5.3943 -0.6842 -0.8763 O 0 0 0 0 0 0 0 0 0 0 0 0
4.0408 -0.532...

Experimental Data

Activity Data

Target Ion Channel
Small Conductance Calcium activated potassium channel (SKCa1)
Uniprot Accession Number
Function
Blocker
Species
Homo sapiens (Human)
IC50
IC50: 12400 nM
EC50
N/A (Not available)
Ki
N/A (Not available)
Kd
N/A (Not available)
Inhibition
N/A (Not available)

Experimental Conditions

pH
pH 7.3
Holding Potential
−80 mV mV
Temperature
22−23 °C
Test Method
Patch-clamping
Test Species
HEK293 cell (Homo sapiens embryonic kidney 293 cell)

Binding Information

Binding Site
Not specified
Binding Site Residue
Not specified

Disease Information

Related Disease
Not specified

References

URL
N/A (Not available)
PMID
Patent
N/A (Not available)

Computed Properties

Heavy Atom Count
21
Rotatable Bonds
2
logP
2.8798
Complexity
77.8016
TPSA (Ų)
79.9
H-Bond Donors
2
H-Bond Acceptors
5
Ring Count
3
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