Ethyl 2-(9-hydroxy-10-oxophenanthren-9-yl)acetate

Details

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Internal ID c9089aab-4840-4a84-a7b7-bda492020590
Taxonomy Benzenoids > Phenanthrenes and derivatives > Hydrophenanthrenes
IUPAC Name ethyl 2-(9-hydroxy-10-oxophenanthren-9-yl)acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H16O4/c1-2-22-16(19)11-18(21)15-10-6-5-8-13(15)12-7-3-4-9-14(12)17(18)20/h3-10,21H,2,11H2,1H3
InChI Key LETAZYCBVRNMHS-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C18H16O4
Molecular Weight 296.30 g/mol
Exact Mass 296.10485899 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.69
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Ethyl 2-(9-hydroxy-10-oxophenanthren-9-yl)acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9905 99.05%
Caco-2 + 0.7129 71.29%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.8477 84.77%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9051 90.51%
OATP1B3 inhibitior + 0.9601 96.01%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.7155 71.55%
P-glycoprotein inhibitior - 0.6669 66.69%
P-glycoprotein substrate - 0.9387 93.87%
CYP3A4 substrate + 0.5302 53.02%
CYP2C9 substrate - 0.7919 79.19%
CYP2D6 substrate - 0.8394 83.94%
CYP3A4 inhibition - 0.8071 80.71%
CYP2C9 inhibition - 0.6267 62.67%
CYP2C19 inhibition - 0.6356 63.56%
CYP2D6 inhibition - 0.9270 92.70%
CYP1A2 inhibition - 0.6645 66.45%
CYP2C8 inhibition - 0.6523 65.23%
CYP inhibitory promiscuity - 0.8612 86.12%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.5959 59.59%
Eye corrosion - 0.9923 99.23%
Eye irritation - 0.6669 66.69%
Skin irritation - 0.7808 78.08%
Skin corrosion - 0.9677 96.77%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8352 83.52%
Micronuclear - 0.5041 50.41%
Hepatotoxicity + 0.6313 63.13%
skin sensitisation - 0.8088 80.88%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.6979 69.79%
Acute Oral Toxicity (c) III 0.6686 66.86%
Estrogen receptor binding + 0.8287 82.87%
Androgen receptor binding + 0.5857 58.57%
Thyroid receptor binding - 0.5425 54.25%
Glucocorticoid receptor binding + 0.8715 87.15%
Aromatase binding + 0.7591 75.91%
PPAR gamma + 0.7228 72.28%
Honey bee toxicity - 0.9478 94.78%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9851 98.51%

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
CHEMBL2581 P07339 Cathepsin D 92.69% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.20% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.96% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.86% 86.33%
CHEMBL221 P23219 Cyclooxygenase-1 89.89% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.66% 91.11%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.73% 82.69%
CHEMBL2535 P11166 Glucose transporter 81.81% 98.75%
CHEMBL4208 P20618 Proteasome component C5 81.38% 90.00%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 81.02% 96.67%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.96% 96.95%
CHEMBL3401 O75469 Pregnane X receptor 80.68% 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.
Toona ciliata

Cross-Links

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PubChem 12454672
LOTUS LTS0098968
wikiData Q104170884