1-(3,6-Dihydroxy-2-methoxy-4-methylphenyl)ethanone

Details

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Internal ID f959dba0-3b8f-4d53-aaad-9bfc3aaed919
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name 1-(3,6-dihydroxy-2-methoxy-4-methylphenyl)ethanone
SMILES (Canonical) CC1=CC(=C(C(=C1O)OC)C(=O)C)O
SMILES (Isomeric) CC1=CC(=C(C(=C1O)OC)C(=O)C)O
InChI InChI=1S/C10H12O4/c1-5-4-7(12)8(6(2)11)10(14-3)9(5)13/h4,12-13H,1-3H3
InChI Key VTSHCKFPQXOAPJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H12O4
Molecular Weight 196.20 g/mol
Exact Mass 196.07355886 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.62
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-(3,6-Dihydroxy-2-methoxy-4-methylphenyl)ethanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9811 98.11%
Caco-2 + 0.5059 50.59%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.8715 87.15%
OATP2B1 inhibitior - 0.8611 86.11%
OATP1B1 inhibitior + 0.9361 93.61%
OATP1B3 inhibitior + 0.9515 95.15%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9593 95.93%
P-glycoprotein inhibitior - 0.9440 94.40%
P-glycoprotein substrate - 0.9727 97.27%
CYP3A4 substrate - 0.6119 61.19%
CYP2C9 substrate - 0.8016 80.16%
CYP2D6 substrate - 0.8116 81.16%
CYP3A4 inhibition - 0.8738 87.38%
CYP2C9 inhibition - 0.9714 97.14%
CYP2C19 inhibition - 0.7216 72.16%
CYP2D6 inhibition - 0.9070 90.70%
CYP1A2 inhibition - 0.6791 67.91%
CYP2C8 inhibition - 0.8236 82.36%
CYP inhibitory promiscuity - 0.7773 77.73%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7454 74.54%
Carcinogenicity (trinary) Non-required 0.6683 66.83%
Eye corrosion + 0.5401 54.01%
Eye irritation + 0.9783 97.83%
Skin irritation + 0.5421 54.21%
Skin corrosion - 0.9267 92.67%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7134 71.34%
Micronuclear + 0.5700 57.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation - 0.7779 77.79%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity - 0.7269 72.69%
Acute Oral Toxicity (c) III 0.6273 62.73%
Estrogen receptor binding - 0.6711 67.11%
Androgen receptor binding - 0.7130 71.30%
Thyroid receptor binding - 0.7374 73.74%
Glucocorticoid receptor binding - 0.7764 77.64%
Aromatase binding - 0.8382 83.82%
PPAR gamma - 0.7321 73.21%
Honey bee toxicity - 0.9642 96.42%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.8492 84.92%

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 97.68% 91.11%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.62% 99.15%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 86.31% 97.21%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.23% 96.09%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 85.11% 93.65%
CHEMBL3401 O75469 Pregnane X receptor 84.64% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.89% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.52% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.33% 95.56%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.75% 96.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.08% 99.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.75% 85.14%
CHEMBL4208 P20618 Proteasome component C5 80.36% 90.00%

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.
Agathis lanceolata
Dracaena concinna
Isodon amethystoides
Neolitsea pulchella
Vigna angularis

Cross-Links

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PubChem 86251457
NPASS NPC185326