4-Hydroxy-5-propionyl-1,3-di-o-methylpyrogallol

Details

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Internal ID d621bd19-eb9f-433b-8454-3d541e3c30a9
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name 1-(2,4-dihydroxy-3,5-dimethoxyphenyl)propan-1-one
SMILES (Canonical) CCC(=O)C1=CC(=C(C(=C1O)OC)O)OC
SMILES (Isomeric) CCC(=O)C1=CC(=C(C(=C1O)OC)O)OC
InChI InChI=1S/C11H14O5/c1-4-7(12)6-5-8(15-2)10(14)11(16-3)9(6)13/h5,13-14H,4H2,1-3H3
InChI Key DMZJXYVZVWKSFA-UHFFFAOYSA-N
Popularity 2 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 1.90
Atomic LogP (AlogP) 1.71
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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CHEBI:70419
1-(2,4-dihydroxy-3,5-dimethoxyphenyl)propan-1-one
Q27138757

2D Structure

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2D Structure of 4-Hydroxy-5-propionyl-1,3-di-o-methylpyrogallol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9308 93.08%
Caco-2 + 0.7162 71.62%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.8071 80.71%
OATP2B1 inhibitior - 0.8602 86.02%
OATP1B1 inhibitior + 0.8829 88.29%
OATP1B3 inhibitior + 0.9486 94.86%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8801 88.01%
P-glycoprotein inhibitior - 0.9328 93.28%
P-glycoprotein substrate - 0.8845 88.45%
CYP3A4 substrate - 0.6320 63.20%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7801 78.01%
CYP3A4 inhibition - 0.5306 53.06%
CYP2C9 inhibition - 0.7215 72.15%
CYP2C19 inhibition + 0.7296 72.96%
CYP2D6 inhibition - 0.6039 60.39%
CYP1A2 inhibition + 0.5159 51.59%
CYP2C8 inhibition + 0.4489 44.89%
CYP inhibitory promiscuity + 0.5000 50.00%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8223 82.23%
Carcinogenicity (trinary) Non-required 0.7205 72.05%
Eye corrosion - 0.8835 88.35%
Eye irritation + 0.9490 94.90%
Skin irritation - 0.6918 69.18%
Skin corrosion - 0.9025 90.25%
Ames mutagenesis - 0.6974 69.74%
Human Ether-a-go-go-Related Gene inhibition - 0.6232 62.32%
Micronuclear - 0.5582 55.82%
Hepatotoxicity - 0.5555 55.55%
skin sensitisation - 0.6649 66.49%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity - 0.9002 90.02%
Acute Oral Toxicity (c) III 0.7253 72.53%
Estrogen receptor binding - 0.4744 47.44%
Androgen receptor binding - 0.7920 79.20%
Thyroid receptor binding - 0.6062 60.62%
Glucocorticoid receptor binding - 0.5853 58.53%
Aromatase binding - 0.8576 85.76%
PPAR gamma - 0.7699 76.99%
Honey bee toxicity - 0.9614 96.14%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.7404 74.04%
Fish aquatic toxicity + 0.7577 75.77%

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 95.09% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.91% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.74% 99.17%
CHEMBL2535 P11166 Glucose transporter 89.08% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.82% 86.33%
CHEMBL4208 P20618 Proteasome component C5 86.25% 90.00%
CHEMBL2581 P07339 Cathepsin D 86.23% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.92% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.85% 94.45%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.81% 96.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.71% 95.50%
CHEMBL1255126 O15151 Protein Mdm4 80.73% 90.20%

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.
Garcia parviflora
Leucanthemopsis pallida

Cross-Links

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PubChem 70698279
NPASS NPC35907
LOTUS LTS0023701
wikiData Q27138757