General
Preferred name
XANTHONE
Synonyms
Xanthone (Genicide) ()
Genicide ()
9H-xanthen-9-one ()
P&D ID
PD002208
CAS
90-47-1
Tags
available
Structure
Probe scores
P&D probe-likeness score
[[ v.score ]]%
Structure formats
[[ format ]]
[[ compound[format === 'MOL' ? 'molblock' : format.toLowerCase()] ]]
Description
(extracted from source data)
DESCRIPTION Xanthone is a monoamine oxidase A (MAO-A) inhibitor with an IC50 of 0.84 ¦ÌM. Xanthon inhibits Norepinephrine (HY-13715) and high-K+-induced vasoconstriction with IC50 values of 60.26 ¦ÌM and 82.9 ¦ÌM, respectively. Xanthon increases intracellular cyclic adenosine 3¡ä,5¡ä-monophosphate (cAMP) content and blocks Ca2+ channels. Xanthone is the scaffold of several pharmacologically active compounds[1][2].
PRICE 29
DESCRIPTION Xanthone (Xanthenone) is currently used as ovicide for codling moth eggs and as a larvicide.
DESCRIPTION Xanthone is a polyketide synthase-derived xanthone, isolated from Mangosteen. It has anti-bacterial, anti-fungal, anti-inflammatory, and anti-viral activities. Xanthone is an activator of Protein kinase C zeta type. (Enamine Bioactive Compounds)
DESCRIPTION Concentration required to inhibit monoamine oxidase activity by 50% (TargetMol Bioactive Compound Library)
Cell lines
1
Organisms
0
Compound Sets
9
AdooQ Bioactive Compound Library
Cayman Chemical Bioactives
Drug Repurposing Hub
Enamine Bioactive Compounds
Enamine BioReference Compounds
MedChem Express Bioactive Compound Library
Selleckchem Bioactive Compound Library
TargetMol Bioactive Compound Library
The Spectrum Collection
External IDs
29
Properties
(calculated by RDKit )
Molecular Weight
196.05
Hydrogen Bond Acceptors
2
Hydrogen Bond Donors
0
Rotatable Bonds
0
Ring Count
3
Aromatic Ring Count
3
cLogP
2.95
TPSA
30.21
Fraction CSP3
0.0
Chiral centers
0.0
Largest ring
6.0
QED
0.52
Structural alerts
0
No structural alerts detected
Custom attributes
(extracted from source data)
MOA
antimalarial agent
Target
Calcium Channel
Monoamine Oxidase
ADC Cytotoxin
Pathway
Membrane Transporter/Ion Channel
Neuronal Signaling
Source data