Dihydroxanthyletin

Details

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Internal ID afbea471-0ed0-43a1-97fb-6fa26764aef5
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Pyranocoumarins > Linear pyranocoumarins
IUPAC Name 2,2-dimethyl-3,4-dihydropyrano[3,2-g]chromen-8-one
SMILES (Canonical) CC1(CCC2=C(O1)C=C3C(=C2)C=CC(=O)O3)C
SMILES (Isomeric) CC1(CCC2=C(O1)C=C3C(=C2)C=CC(=O)O3)C
InChI InChI=1S/C14H14O3/c1-14(2)6-5-10-7-9-3-4-13(15)16-11(9)8-12(10)17-14/h3-4,7-8H,5-6H2,1-2H3
InChI Key OHVLVQZSSLHFMS-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C14H14O3
Molecular Weight 230.26 g/mol
Exact Mass 230.094294304 g/mol
Topological Polar Surface Area (TPSA) 35.50 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.90
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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CHEMBL1934198
SCHEMBL4741095
BDBM50361394
AKOS000278012

2D Structure

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2D Structure of Dihydroxanthyletin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9946 99.46%
Caco-2 + 0.8557 85.57%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.7578 75.78%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9196 91.96%
OATP1B3 inhibitior + 0.9819 98.19%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8640 86.40%
P-glycoprotein inhibitior - 0.9315 93.15%
P-glycoprotein substrate - 0.8603 86.03%
CYP3A4 substrate - 0.5496 54.96%
CYP2C9 substrate - 0.6794 67.94%
CYP2D6 substrate - 0.8056 80.56%
CYP3A4 inhibition - 0.8676 86.76%
CYP2C9 inhibition - 0.6336 63.36%
CYP2C19 inhibition - 0.6153 61.53%
CYP2D6 inhibition - 0.7773 77.73%
CYP1A2 inhibition + 0.5788 57.88%
CYP2C8 inhibition - 0.8565 85.65%
CYP inhibitory promiscuity - 0.9102 91.02%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5803 58.03%
Eye corrosion - 0.9790 97.90%
Eye irritation - 0.5222 52.22%
Skin irritation - 0.6604 66.04%
Skin corrosion - 0.9089 90.89%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7078 70.78%
Micronuclear - 0.7941 79.41%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation - 0.6900 69.00%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.5882 58.82%
Acute Oral Toxicity (c) III 0.7316 73.16%
Estrogen receptor binding + 0.7933 79.33%
Androgen receptor binding + 0.5524 55.24%
Thyroid receptor binding - 0.5601 56.01%
Glucocorticoid receptor binding + 0.6023 60.23%
Aromatase binding + 0.7393 73.93%
PPAR gamma + 0.6020 60.20%
Honey bee toxicity - 0.8798 87.98%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9538 95.38%

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 96.71% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.45% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.18% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.61% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.08% 95.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.97% 90.71%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 85.72% 85.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.05% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.02% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 82.41% 94.73%

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.
Ammi majus
Zanthoxylum spinosum

Cross-Links

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PubChem 10466390
NPASS NPC111347
LOTUS LTS0242500
wikiData Q104402661