Lichexanthone

Details

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Internal ID 7ac3f63d-6486-45c9-9a38-f214762078e8
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1-hydroxy-3,6-dimethoxy-8-methylxanthen-9-one
SMILES (Canonical) CC1=CC(=CC2=C1C(=O)C3=C(C=C(C=C3O2)OC)O)OC
SMILES (Isomeric) CC1=CC(=CC2=C1C(=O)C3=C(C=C(C=C3O2)OC)O)OC
InChI InChI=1S/C16H14O5/c1-8-4-9(19-2)6-12-14(8)16(18)15-11(17)5-10(20-3)7-13(15)21-12/h4-7,17H,1-3H3
InChI Key QDLAGTHXVHQKRE-UHFFFAOYSA-N
Popularity 12 references in papers

Physical and Chemical Properties

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Molecular Formula C16H14O5
Molecular Weight 286.28 g/mol
Exact Mass 286.08412354 g/mol
Topological Polar Surface Area (TPSA) 65.00 Ų
XlogP 3.50
Atomic LogP (AlogP) 2.98
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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15222-53-4
1-Hydroxy-3,6-dimethoxy-8-methyl-9H-xanthen-9-one
1-hydroxy-3,6-dimethoxy-8-methylxanthen-9-one
Xanthen-9-one, 1-hydroxy-3,6-dimethoxy-8-methyl-
9H-Xanthen-9-one, 1-hydroxy-3,6-dimethoxy-8-methyl-
CHEBI:67821
92O5D9Z07W
LICHEXANTHONE B804322K045
NSC 288657
NSC-288657
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Lichexanthone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9841 98.41%
Caco-2 + 0.8919 89.19%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.6678 66.78%
OATP2B1 inhibitior - 0.8581 85.81%
OATP1B1 inhibitior + 0.9288 92.88%
OATP1B3 inhibitior + 0.9873 98.73%
MATE1 inhibitior - 0.6000 60.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.6309 63.09%
P-glycoprotein inhibitior - 0.4712 47.12%
P-glycoprotein substrate - 0.9464 94.64%
CYP3A4 substrate - 0.5469 54.69%
CYP2C9 substrate - 0.6360 63.60%
CYP2D6 substrate - 0.8410 84.10%
CYP3A4 inhibition + 0.5994 59.94%
CYP2C9 inhibition - 0.9188 91.88%
CYP2C19 inhibition - 0.6082 60.82%
CYP2D6 inhibition - 0.8535 85.35%
CYP1A2 inhibition + 0.9359 93.59%
CYP2C8 inhibition - 0.7101 71.01%
CYP inhibitory promiscuity - 0.6092 60.92%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9113 91.13%
Carcinogenicity (trinary) Non-required 0.5650 56.50%
Eye corrosion - 0.9482 94.82%
Eye irritation + 0.9277 92.77%
Skin irritation - 0.7107 71.07%
Skin corrosion - 0.9915 99.15%
Ames mutagenesis + 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6967 69.67%
Micronuclear + 0.8200 82.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation - 0.9602 96.02%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.6176 61.76%
Acute Oral Toxicity (c) III 0.5893 58.93%
Estrogen receptor binding + 0.8097 80.97%
Androgen receptor binding + 0.7109 71.09%
Thyroid receptor binding + 0.6862 68.62%
Glucocorticoid receptor binding + 0.7717 77.17%
Aromatase binding + 0.8585 85.85%
PPAR gamma + 0.7408 74.08%
Honey bee toxicity - 0.8985 89.85%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.7667 76.67%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.90% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.05% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.45% 85.14%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 93.06% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.94% 94.00%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 91.02% 93.65%
CHEMBL3401 O75469 Pregnane X receptor 87.96% 94.73%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.13% 93.99%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.70% 89.00%
CHEMBL2581 P07339 Cathepsin D 86.20% 98.95%
CHEMBL4208 P20618 Proteasome component C5 85.89% 90.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.30% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.66% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.25% 99.17%
CHEMBL3194 P02766 Transthyretin 82.78% 90.71%
CHEMBL2535 P11166 Glucose transporter 80.03% 98.75%

Cross-Links

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PubChem 5358904
NPASS NPC310340
LOTUS LTS0074910
wikiData Q27136297