Phellodenol A

Details

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Internal ID 7f990c4f-4be3-46da-8939-2e78948cb22e
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Hydroxycoumarins > 7-hydroxycoumarins
IUPAC Name 7-hydroxy-6-(2-hydroxyethyl)chromen-2-one
SMILES (Canonical) C1=CC(=O)OC2=CC(=C(C=C21)CCO)O
SMILES (Isomeric) C1=CC(=O)OC2=CC(=C(C=C21)CCO)O
InChI InChI=1S/C11H10O4/c12-4-3-7-5-8-1-2-11(14)15-10(8)6-9(7)13/h1-2,5-6,12-13H,3-4H2
InChI Key UNMQLUGEYMJJSH-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C11H10O4
Molecular Weight 206.19 g/mol
Exact Mass 206.05790880 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 1.10
Atomic LogP (AlogP) 1.03
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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612086-85-8
2H-1-Benzopyran-2-one, 7-hydroxy-6-(2-hydroxyethyl)-
7-hydroxy-6-(2-hydroxyethyl)-2H-chromen-2-one
CHEMBL3935284

2D Structure

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2D Structure of Phellodenol A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9071 90.71%
Caco-2 + 0.7055 70.55%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.8043 80.43%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8721 87.21%
OATP1B3 inhibitior + 0.9239 92.39%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9292 92.92%
P-glycoprotein inhibitior - 0.9796 97.96%
P-glycoprotein substrate - 0.9095 90.95%
CYP3A4 substrate - 0.6680 66.80%
CYP2C9 substrate - 0.5981 59.81%
CYP2D6 substrate - 0.8001 80.01%
CYP3A4 inhibition - 0.8646 86.46%
CYP2C9 inhibition - 0.7253 72.53%
CYP2C19 inhibition - 0.6605 66.05%
CYP2D6 inhibition - 0.8367 83.67%
CYP1A2 inhibition - 0.6948 69.48%
CYP2C8 inhibition - 0.8405 84.05%
CYP inhibitory promiscuity - 0.8783 87.83%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6639 66.39%
Eye corrosion - 0.9927 99.27%
Eye irritation + 0.9587 95.87%
Skin irritation - 0.7559 75.59%
Skin corrosion - 0.9668 96.68%
Ames mutagenesis - 0.6737 67.37%
Human Ether-a-go-go-Related Gene inhibition - 0.7158 71.58%
Micronuclear - 0.5367 53.67%
Hepatotoxicity - 0.5842 58.42%
skin sensitisation - 0.8613 86.13%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity - 0.5912 59.12%
Acute Oral Toxicity (c) III 0.4124 41.24%
Estrogen receptor binding + 0.5265 52.65%
Androgen receptor binding + 0.6031 60.31%
Thyroid receptor binding - 0.6854 68.54%
Glucocorticoid receptor binding + 0.7176 71.76%
Aromatase binding + 0.6731 67.31%
PPAR gamma + 0.8414 84.14%
Honey bee toxicity - 0.9580 95.80%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity + 0.6791 67.91%

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 98.77% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.19% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.96% 94.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 87.79% 90.71%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.97% 99.15%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 85.40% 86.92%
CHEMBL3401 O75469 Pregnane X receptor 84.64% 94.73%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 83.96% 83.57%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.81% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.81% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.32% 86.33%

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.
Fatoua villosa
Phellodendron amurense

Cross-Links

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PubChem 10910685
NPASS NPC232623
LOTUS LTS0011708
wikiData Q105276055