3-Hydroxy-1-(2-hydroxy-4,5-dimethoxyphenyl)propan-1-one

Details

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Internal ID 44134147-506e-4ea2-9df8-d434f86c22b7
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name 3-hydroxy-1-(2-hydroxy-4,5-dimethoxyphenyl)propan-1-one
SMILES (Canonical) COC1=C(C=C(C(=C1)C(=O)CCO)O)OC
SMILES (Isomeric) COC1=C(C=C(C(=C1)C(=O)CCO)O)OC
InChI InChI=1S/C11H14O5/c1-15-10-5-7(8(13)3-4-12)9(14)6-11(10)16-2/h5-6,12,14H,3-4H2,1-2H3
InChI Key YBLJMFGWUGQHDR-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H14O5
Molecular Weight 226.23 g/mol
Exact Mass 226.08412354 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 1.00
Atomic LogP (AlogP) 0.97
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-Hydroxy-1-(2-hydroxy-4,5-dimethoxyphenyl)propan-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9639 96.39%
Caco-2 + 0.8329 83.29%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.8952 89.52%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8815 88.15%
OATP1B3 inhibitior + 0.9555 95.55%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8683 86.83%
P-glycoprotein inhibitior - 0.9517 95.17%
P-glycoprotein substrate - 0.9112 91.12%
CYP3A4 substrate - 0.6695 66.95%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7770 77.70%
CYP3A4 inhibition - 0.8136 81.36%
CYP2C9 inhibition - 0.7975 79.75%
CYP2C19 inhibition - 0.7132 71.32%
CYP2D6 inhibition - 0.9082 90.82%
CYP1A2 inhibition + 0.5768 57.68%
CYP2C8 inhibition - 0.8393 83.93%
CYP inhibitory promiscuity - 0.8422 84.22%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.8200 82.00%
Carcinogenicity (trinary) Non-required 0.7762 77.62%
Eye corrosion - 0.9534 95.34%
Eye irritation + 0.9793 97.93%
Skin irritation - 0.6263 62.63%
Skin corrosion - 0.9545 95.45%
Ames mutagenesis - 0.7537 75.37%
Human Ether-a-go-go-Related Gene inhibition - 0.7131 71.31%
Micronuclear - 0.8123 81.23%
Hepatotoxicity - 0.5445 54.45%
skin sensitisation - 0.6353 63.53%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity + 0.4790 47.90%
Acute Oral Toxicity (c) III 0.8073 80.73%
Estrogen receptor binding - 0.5651 56.51%
Androgen receptor binding - 0.9315 93.15%
Thyroid receptor binding - 0.5900 59.00%
Glucocorticoid receptor binding - 0.5850 58.50%
Aromatase binding - 0.6164 61.64%
PPAR gamma - 0.7060 70.60%
Honey bee toxicity - 0.9494 94.94%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.8949 89.49%
Fish aquatic toxicity - 0.6964 69.64%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.57% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.56% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.01% 99.17%
CHEMBL4208 P20618 Proteasome component C5 88.03% 90.00%
CHEMBL2535 P11166 Glucose transporter 87.01% 98.75%
CHEMBL2581 P07339 Cathepsin D 86.80% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.54% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.07% 95.56%
CHEMBL1255126 O15151 Protein Mdm4 82.32% 90.20%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.92% 91.07%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.50% 94.00%

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.
Codonopsis cordifolioidea

Cross-Links

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PubChem 162867017
LOTUS LTS0034829
wikiData Q105345907