Microxanthone

Details

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Internal ID e995dace-50e4-4081-b311-4c6bba693ab2
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name methyl 4,8-dihydroxy-6-methyl-9-oxoxanthene-1-carboxylate
SMILES (Canonical) CC1=CC(=C2C(=C1)OC3=C(C=CC(=C3C2=O)C(=O)OC)O)O
SMILES (Isomeric) CC1=CC(=C2C(=C1)OC3=C(C=CC(=C3C2=O)C(=O)OC)O)O
InChI InChI=1S/C16H12O6/c1-7-5-10(18)13-11(6-7)22-15-9(17)4-3-8(16(20)21-2)12(15)14(13)19/h3-6,17-18H,1-2H3
InChI Key ROBVUHWNBUASTR-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H12O6
Molecular Weight 300.26 g/mol
Exact Mass 300.06338810 g/mol
Topological Polar Surface Area (TPSA) 93.10 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.45
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Microxanthone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9158 91.58%
Caco-2 + 0.5753 57.53%
Blood Brain Barrier - 0.9000 90.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.7069 70.69%
OATP2B1 inhibitior - 0.6983 69.83%
OATP1B1 inhibitior + 0.9114 91.14%
OATP1B3 inhibitior + 0.8878 88.78%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.6489 64.89%
P-glycoprotein inhibitior - 0.6784 67.84%
P-glycoprotein substrate - 0.8804 88.04%
CYP3A4 substrate + 0.5225 52.25%
CYP2C9 substrate - 0.5626 56.26%
CYP2D6 substrate - 0.8850 88.50%
CYP3A4 inhibition - 0.8504 85.04%
CYP2C9 inhibition - 0.8237 82.37%
CYP2C19 inhibition - 0.8951 89.51%
CYP2D6 inhibition - 0.8472 84.72%
CYP1A2 inhibition - 0.5722 57.22%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity - 0.8210 82.10%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5730 57.30%
Eye corrosion - 0.9610 96.10%
Eye irritation + 0.8475 84.75%
Skin irritation - 0.7500 75.00%
Skin corrosion - 0.9743 97.43%
Ames mutagenesis + 0.7936 79.36%
Human Ether-a-go-go-Related Gene inhibition - 0.6151 61.51%
Micronuclear + 0.8900 89.00%
Hepatotoxicity + 0.5976 59.76%
skin sensitisation - 0.9490 94.90%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity + 0.5171 51.71%
Acute Oral Toxicity (c) III 0.6374 63.74%
Estrogen receptor binding + 0.8944 89.44%
Androgen receptor binding + 0.8242 82.42%
Thyroid receptor binding - 0.6244 62.44%
Glucocorticoid receptor binding + 0.8996 89.96%
Aromatase binding + 0.7669 76.69%
PPAR gamma + 0.7582 75.82%
Honey bee toxicity - 0.9406 94.06%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.7866 78.66%
Fish aquatic toxicity + 0.8695 86.95%

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 97.92% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 92.61% 94.73%
CHEMBL4040 P28482 MAP kinase ERK2 91.10% 83.82%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.30% 94.00%
CHEMBL2581 P07339 Cathepsin D 90.29% 98.95%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 90.24% 81.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.08% 99.23%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 88.94% 93.65%
CHEMBL1951 P21397 Monoamine oxidase A 87.78% 91.49%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.53% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.38% 95.56%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 85.94% 94.42%
CHEMBL2535 P11166 Glucose transporter 85.46% 98.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.37% 94.45%
CHEMBL4208 P20618 Proteasome component C5 84.02% 90.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.50% 89.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 81.43% 94.80%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 81.39% 99.15%
CHEMBL3194 P02766 Transthyretin 80.98% 90.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.88% 99.17%
CHEMBL340 P08684 Cytochrome P450 3A4 80.78% 91.19%

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.
There are no matching plants.

Cross-Links

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PubChem 102300482
LOTUS LTS0188066
wikiData Q77514031