3-(2-Hydroxy-3,4-dimethoxyphenyl)propanoic acid

Details

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Internal ID 7aea71c7-59fe-4029-b2dd-3774730fb6bc
Taxonomy Phenylpropanoids and polyketides > Phenylpropanoic acids
IUPAC Name 3-(2-hydroxy-3,4-dimethoxyphenyl)propanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H14O5/c1-15-8-5-3-7(4-6-9(12)13)10(14)11(8)16-2/h3,5,14H,4,6H2,1-2H3,(H,12,13)
InChI Key QLACLEPYLWLNTD-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 1.30
Atomic LogP (AlogP) 1.43
H-Bond Acceptor 4
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-(2-Hydroxy-3,4-dimethoxyphenyl)propanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9387 93.87%
Caco-2 + 0.8003 80.03%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.8810 88.10%
OATP2B1 inhibitior - 0.8573 85.73%
OATP1B1 inhibitior + 0.9267 92.67%
OATP1B3 inhibitior + 0.9409 94.09%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9156 91.56%
P-glycoprotein inhibitior - 0.9829 98.29%
P-glycoprotein substrate - 0.9108 91.08%
CYP3A4 substrate - 0.5841 58.41%
CYP2C9 substrate + 0.5641 56.41%
CYP2D6 substrate - 0.7778 77.78%
CYP3A4 inhibition - 0.9505 95.05%
CYP2C9 inhibition - 0.8480 84.80%
CYP2C19 inhibition - 0.7716 77.16%
CYP2D6 inhibition - 0.9144 91.44%
CYP1A2 inhibition - 0.6693 66.93%
CYP2C8 inhibition + 0.4565 45.65%
CYP inhibitory promiscuity - 0.9073 90.73%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7815 78.15%
Carcinogenicity (trinary) Non-required 0.7301 73.01%
Eye corrosion - 0.9440 94.40%
Eye irritation + 0.9090 90.90%
Skin irritation - 0.5643 56.43%
Skin corrosion - 0.8912 89.12%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5454 54.54%
Micronuclear - 0.6265 62.65%
Hepatotoxicity + 0.5034 50.34%
skin sensitisation - 0.8244 82.44%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.8514 85.14%
Acute Oral Toxicity (c) III 0.6260 62.60%
Estrogen receptor binding - 0.6562 65.62%
Androgen receptor binding - 0.7355 73.55%
Thyroid receptor binding - 0.6477 64.77%
Glucocorticoid receptor binding - 0.6484 64.84%
Aromatase binding - 0.7840 78.40%
PPAR gamma - 0.7386 73.86%
Honey bee toxicity - 0.9692 96.92%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.8929 89.29%
Fish aquatic toxicity + 0.6850 68.50%

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
CHEMBL1255126 O15151 Protein Mdm4 96.72% 90.20%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.34% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.95% 91.11%
CHEMBL2581 P07339 Cathepsin D 92.48% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.39% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.02% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.80% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.16% 95.56%
CHEMBL4208 P20618 Proteasome component C5 81.27% 90.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 117325047
LOTUS LTS0031586
wikiData Q105223442