3,5-Dihydroxy-4-methoxy-xanthen-9-one

Details

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Internal ID 40105494-7a57-42f1-819a-680fd4fbea76
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 3,5-dihydroxy-4-methoxyxanthen-9-one
SMILES (Canonical) COC1=C(C=CC2=C1OC3=C(C2=O)C=CC=C3O)O
SMILES (Isomeric) COC1=C(C=CC2=C1OC3=C(C2=O)C=CC=C3O)O
InChI InChI=1S/C14H10O5/c1-18-14-10(16)6-5-8-11(17)7-3-2-4-9(15)12(7)19-13(8)14/h2-6,15-16H,1H3
InChI Key JNQLXRMQDHWYIN-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C14H10O5
Molecular Weight 258.23 g/mol
Exact Mass 258.05282342 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.37
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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3,5-Dihydroxy-4-methoxy-9H-xanthen-9-one

2D Structure

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2D Structure of 3,5-Dihydroxy-4-methoxy-xanthen-9-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9711 97.11%
Caco-2 + 0.5597 55.97%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.7377 73.77%
OATP2B1 inhibitior - 0.7136 71.36%
OATP1B1 inhibitior + 0.9641 96.41%
OATP1B3 inhibitior + 0.9934 99.34%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.7413 74.13%
P-glycoprotein inhibitior - 0.7189 71.89%
P-glycoprotein substrate - 0.9162 91.62%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.8382 83.82%
CYP2D6 substrate - 0.7720 77.20%
CYP3A4 inhibition - 0.7181 71.81%
CYP2C9 inhibition - 0.5805 58.05%
CYP2C19 inhibition + 0.7909 79.09%
CYP2D6 inhibition - 0.7438 74.38%
CYP1A2 inhibition + 0.9811 98.11%
CYP2C8 inhibition - 0.7345 73.45%
CYP inhibitory promiscuity + 0.6572 65.72%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5675 56.75%
Eye corrosion - 0.9577 95.77%
Eye irritation + 0.8636 86.36%
Skin irritation - 0.5200 52.00%
Skin corrosion - 0.9642 96.42%
Ames mutagenesis + 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7660 76.60%
Micronuclear + 0.9200 92.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.9205 92.05%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.6327 63.27%
Acute Oral Toxicity (c) III 0.8197 81.97%
Estrogen receptor binding + 0.8143 81.43%
Androgen receptor binding + 0.5390 53.90%
Thyroid receptor binding + 0.6672 66.72%
Glucocorticoid receptor binding + 0.8966 89.66%
Aromatase binding + 0.8153 81.53%
PPAR gamma + 0.6382 63.82%
Honey bee toxicity - 0.9128 91.28%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.8258 82.58%

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 98.15% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.57% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.17% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.41% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.18% 99.15%
CHEMBL3192 Q9BY41 Histone deacetylase 8 89.89% 93.99%
CHEMBL2581 P07339 Cathepsin D 89.75% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.76% 89.00%
CHEMBL2535 P11166 Glucose transporter 86.53% 98.75%
CHEMBL3401 O75469 Pregnane X receptor 85.53% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.06% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.71% 86.33%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 81.38% 80.78%
CHEMBL1937 Q92769 Histone deacetylase 2 80.96% 94.75%
CHEMBL1907 P15144 Aminopeptidase N 80.24% 93.31%

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.
Artemisia anomala
Eupatorium glehnii
Leptochloa digitata
Pinus heldreichii
Piper umbellatum
Senecio brasiliensis
Tovomita krukovii

Cross-Links

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PubChem 5493669
NPASS NPC257298
LOTUS LTS0164525
wikiData Q105132069