6-Hydroxy-1,2,5-trimethoxyxanthen-9-one

Details

• Internal ID: 77dd83e0-f8d0-42ca-a0d9-d99a6f3a5674
• Taxonomy: Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
• IUPAC Name: 6-hydroxy-1,2,5-trimethoxyxanthen-9-one
• SMILES (Canonical): COC1=C(C2=C(C=C1)OC3=C(C2=O)C=CC(=C3OC)O)OC
• SMILES (Isomeric): COC1=C(C2=C(C=C1)OC3=C(C2=O)C=CC(=C3OC)O)OC
• InChI: InChI=1S/C16H14O6/c1-19-11-7-6-10-12(16(11)21-3)13(18)8-4-5-9(17)15(20-2)14(8)22-10/h4-7,17H,1-3H3
• InChI Key: BKSUQMQAIGVECD-UHFFFAOYSA-N
• Popularity: 1 reference in papers

Physical and Chemical Properties

• Molecular Formula: C₁₆H₁₄O₆
• Molecular Weight: 302.28 g/mol
• Exact Mass: 302.07903816 g/mol
• Topological Polar Surface Area (TPSA): 74.20 Ų
• XlogP: 2.50
• Atomic LogP (AlogP): 2.68
• H-Bond Acceptor: 6
• H-Bond Donor: 1
• Rotatable Bonds: 3

Synonyms

There are no found synonyms.

2D Structure

ADMET Properties (via admetSAR 2)

Target	Value	Probability (raw)	Probability (%)
Human Intestinal Absorption	+	0.9769	97.69%
Caco-2	+	0.7566	75.66%
Blood Brain Barrier	-	0.7750	77.50%
Human oral bioavailability	+	0.5857	58.57%
Subcellular localzation	Mitochondria	0.6863	68.63%
OATP2B1 inhibitior	-	0.5857	58.57%
OATP1B1 inhibitior	+	0.9638	96.38%
OATP1B3 inhibitior	+	0.9884	98.84%
MATE1 inhibitior	-	0.7800	78.00%
OCT2 inhibitior	-	0.9750	97.50%
BSEP inhibitior	-	0.6908	69.08%
P-glycoprotein inhibitior	-	0.5376	53.76%
P-glycoprotein substrate	-	0.8870	88.70%
CYP3A4 substrate	-	0.5313	53.13%
CYP2C9 substrate	-	0.8382	83.82%
CYP2D6 substrate	-	0.7720	77.20%
CYP3A4 inhibition	-	0.6511	65.11%
CYP2C9 inhibition	-	0.9806	98.06%
CYP2C19 inhibition	-	0.6277	62.77%
CYP2D6 inhibition	-	0.8588	85.88%
CYP1A2 inhibition	+	0.9585	95.85%
CYP2C8 inhibition	-	0.6487	64.87%
CYP inhibitory promiscuity	-	0.5523	55.23%
UGT catelyzed	-	0.6000	60.00%
Carcinogenicity (binary)	-	0.9900	99.00%
Carcinogenicity (trinary)	Non-required	0.6004	60.04%
Eye corrosion	-	0.9679	96.79%
Eye irritation	+	0.8424	84.24%
Skin irritation	-	0.6803	68.03%
Skin corrosion	-	0.9860	98.60%
Ames mutagenesis	+	0.6536	65.36%
Human Ether-a-go-go-Related Gene inhibition	-	0.5471	54.71%
Micronuclear	+	0.8359	83.59%
Hepatotoxicity	+	0.5750	57.50%
skin sensitisation	-	0.9331	93.31%
Respiratory toxicity	+	0.6111	61.11%
Reproductive toxicity	+	0.8111	81.11%
Mitochondrial toxicity	+	0.5375	53.75%
Nephrotoxicity	-	0.7074	70.74%
Acute Oral Toxicity (c)	II	0.5755	57.55%
Estrogen receptor binding	+	0.8893	88.93%
Androgen receptor binding	+	0.6984	69.84%
Thyroid receptor binding	+	0.6775	67.75%
Glucocorticoid receptor binding	+	0.8345	83.45%
Aromatase binding	+	0.8670	86.70%
PPAR gamma	+	0.7043	70.43%
Honey bee toxicity	-	0.8843	88.43%
Biodegradation	-	0.7750	77.50%
Crustacea aquatic toxicity	-	0.6000	60.00%
Fish aquatic toxicity	+	0.8585	85.85%

Targets

Proven Targets:

No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID	UniProt ID	Name	Probability	Model accuracy
CHEMBL5619	P27695	DNA-(apurinic or apyrimidinic site) lyase	96.67%	91.11%
CHEMBL3108638	O15164	Transcription intermediary factor 1-alpha	94.35%	95.56%
CHEMBL2635	P51452	Dual specificity protein phosphatase 3	93.84%	94.00%
CHEMBL4203	Q9HAZ1	Dual specificity protein kinase CLK4	91.86%	94.45%
CHEMBL3038477	P67870	Casein kinase II alpha/beta	91.14%	99.23%
CHEMBL1806	P11388	DNA topoisomerase II alpha	90.74%	89.00%
CHEMBL2085	P14174	Macrophage migration inhibitory factor	90.74%	80.78%
CHEMBL3192	Q9BY41	Histone deacetylase 8	87.46%	93.99%
CHEMBL1255126	O15151	Protein Mdm4	87.11%	90.20%
CHEMBL2535	P11166	Glucose transporter	87.09%	98.75%
CHEMBL1951	P21397	Monoamine oxidase A	84.71%	91.49%
CHEMBL1293249	Q13887	Kruppel-like factor 5	83.99%	86.33%
CHEMBL2581	P07339	Cathepsin D	83.49%	98.95%
CHEMBL3194	P02766	Transthyretin	82.02%	90.71%
CHEMBL1860	P10827	Thyroid hormone receptor alpha	80.84%	99.15%

Plants that contains it

• Calophyllum teysmannii

Cross-Links

• PubChem: 101717280
• LOTUS: LTS0061615
• wikiData: Q104937779