1-Hydroxy-5,6-dimethoxyxanthone

Details

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Internal ID c27b0c59-d3ef-4acb-acda-47ec64fdb4ad
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1-hydroxy-5,6-dimethoxyxanthen-9-one
SMILES (Canonical) COC1=C(C2=C(C=C1)C(=O)C3=C(C=CC=C3O2)O)OC
SMILES (Isomeric) COC1=C(C2=C(C=C1)C(=O)C3=C(C=CC=C3O2)O)OC
InChI InChI=1S/C15H12O5/c1-18-11-7-6-8-13(17)12-9(16)4-3-5-10(12)20-14(8)15(11)19-2/h3-7,16H,1-2H3
InChI Key GPLUNIIWKODZMV-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C15H12O5
Molecular Weight 272.25 g/mol
Exact Mass 272.06847348 g/mol
Topological Polar Surface Area (TPSA) 65.00 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.67
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-Hydroxy-5,6-dimethoxyxanthone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9791 97.91%
Caco-2 + 0.8816 88.16%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.7024 70.24%
OATP2B1 inhibitior - 0.7248 72.48%
OATP1B1 inhibitior + 0.9541 95.41%
OATP1B3 inhibitior + 0.9932 99.32%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.5621 56.21%
P-glycoprotein inhibitior - 0.4758 47.58%
P-glycoprotein substrate - 0.8466 84.66%
CYP3A4 substrate + 0.5295 52.95%
CYP2C9 substrate - 0.6401 64.01%
CYP2D6 substrate - 0.8296 82.96%
CYP3A4 inhibition + 0.5215 52.15%
CYP2C9 inhibition - 0.8938 89.38%
CYP2C19 inhibition + 0.6902 69.02%
CYP2D6 inhibition - 0.7703 77.03%
CYP1A2 inhibition + 0.9595 95.95%
CYP2C8 inhibition + 0.4512 45.12%
CYP inhibitory promiscuity + 0.5264 52.64%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6210 62.10%
Eye corrosion - 0.9551 95.51%
Eye irritation + 0.8707 87.07%
Skin irritation - 0.5807 58.07%
Skin corrosion - 0.9822 98.22%
Ames mutagenesis + 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5673 56.73%
Micronuclear + 0.8959 89.59%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation - 0.9125 91.25%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity + 0.4734 47.34%
Acute Oral Toxicity (c) III 0.4994 49.94%
Estrogen receptor binding + 0.8275 82.75%
Androgen receptor binding + 0.7232 72.32%
Thyroid receptor binding + 0.6835 68.35%
Glucocorticoid receptor binding + 0.8027 80.27%
Aromatase binding + 0.7452 74.52%
PPAR gamma + 0.7551 75.51%
Honey bee toxicity - 0.9299 92.99%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6049 60.49%
Fish aquatic toxicity + 0.8492 84.92%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.42% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 94.43% 93.99%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.15% 91.11%
CHEMBL1255126 O15151 Protein Mdm4 93.91% 90.20%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 93.24% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.91% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.48% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.45% 94.45%
CHEMBL4040 P28482 MAP kinase ERK2 91.28% 83.82%
CHEMBL2581 P07339 Cathepsin D 91.07% 98.95%
CHEMBL2535 P11166 Glucose transporter 90.86% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.82% 86.33%
CHEMBL1937 Q92769 Histone deacetylase 2 84.26% 94.75%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 82.68% 80.78%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 81.84% 94.03%
CHEMBL3401 O75469 Pregnane X receptor 81.67% 94.73%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.36% 95.50%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Calophyllum thwaitesii
Cratoxylum cochinchinense

Cross-Links

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PubChem 90906816
LOTUS LTS0234224
wikiData Q105014987