2,2,2-Trideuterio-1-(2-hydroxy-4-methoxyphenyl)ethanone

Details

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Internal ID b4d709b7-995d-4cb9-896f-2e8c8b4dc394
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name 2,2,2-trideuterio-1-(2-hydroxy-4-methoxyphenyl)ethanone
SMILES (Canonical) CC(=O)C1=C(C=C(C=C1)OC)O
SMILES (Isomeric) [2H]C([2H])([2H])C(=O)C1=C(C=C(C=C1)OC)O
InChI InChI=1S/C9H10O3/c1-6(10)8-4-3-7(12-2)5-9(8)11/h3-5,11H,1-2H3/i1D3
InChI Key UILPJVPSNHJFIK-FIBGUPNXSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C9H10O3
Molecular Weight 169.19 g/mol
Exact Mass 169.081824415 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 2.00
Atomic LogP (AlogP) 1.60
H-Bond Acceptor 3
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 2,2,2-Trideuterio-1-(2-hydroxy-4-methoxyphenyl)ethanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9928 99.28%
Caco-2 + 0.8781 87.81%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.9484 94.84%
OATP2B1 inhibitior - 0.8634 86.34%
OATP1B1 inhibitior + 0.9593 95.93%
OATP1B3 inhibitior + 0.9902 99.02%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9259 92.59%
P-glycoprotein inhibitior - 0.9514 95.14%
P-glycoprotein substrate - 0.9454 94.54%
CYP3A4 substrate - 0.6002 60.02%
CYP2C9 substrate - 0.8016 80.16%
CYP2D6 substrate - 0.8116 81.16%
CYP3A4 inhibition - 0.9023 90.23%
CYP2C9 inhibition - 0.9794 97.94%
CYP2C19 inhibition - 0.5112 51.12%
CYP2D6 inhibition - 0.9502 95.02%
CYP1A2 inhibition - 0.5947 59.47%
CYP2C8 inhibition - 0.7961 79.61%
CYP inhibitory promiscuity - 0.8570 85.70%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6718 67.18%
Carcinogenicity (trinary) Non-required 0.6657 66.57%
Eye corrosion + 0.9118 91.18%
Eye irritation + 0.8674 86.74%
Skin irritation + 0.8496 84.96%
Skin corrosion - 0.9347 93.47%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7884 78.84%
Micronuclear - 0.5767 57.67%
Hepatotoxicity - 0.7935 79.35%
skin sensitisation - 0.7205 72.05%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity - 0.5925 59.25%
Acute Oral Toxicity (c) III 0.8671 86.71%
Estrogen receptor binding - 0.5435 54.35%
Androgen receptor binding - 0.6005 60.05%
Thyroid receptor binding + 0.5626 56.26%
Glucocorticoid receptor binding - 0.5994 59.94%
Aromatase binding - 0.5364 53.64%
PPAR gamma + 0.7082 70.82%
Honey bee toxicity - 0.9514 95.14%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.8390 83.90%

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 97.71% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.35% 96.09%
CHEMBL4208 P20618 Proteasome component C5 92.16% 90.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.66% 99.15%
CHEMBL2535 P11166 Glucose transporter 88.91% 98.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.59% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.38% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.17% 99.17%
CHEMBL2581 P07339 Cathepsin D 85.31% 98.95%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 84.49% 91.07%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.74% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.03% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 80.39% 94.73%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.31% 95.50%

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.
Angelica dahurica
Morus alba
Paeonia anomala subsp. veitchii
Paeonia suffruticosa
Primula latifolia

Cross-Links

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PubChem 11816097
NPASS NPC233538