Ethyl 2,4-dihydroxy-3,5,6-trimethylbenzoate

Details

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Internal ID e04fda5c-6b42-437d-9d1e-c826452bb9f5
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > p-Hydroxybenzoic acid esters > p-Hydroxybenzoic acid alkyl esters
IUPAC Name ethyl 2,4-dihydroxy-3,5,6-trimethylbenzoate
SMILES (Canonical) CCOC(=O)C1=C(C(=C(C(=C1C)C)O)C)O
SMILES (Isomeric) CCOC(=O)C1=C(C(=C(C(=C1C)C)O)C)O
InChI InChI=1S/C12H16O4/c1-5-16-12(15)9-6(2)7(3)10(13)8(4)11(9)14/h13-14H,5H2,1-4H3
InChI Key NHKFCDQZJNYGKZ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C12H16O4
Molecular Weight 224.25 g/mol
Exact Mass 224.10485899 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.20
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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81345-10-0
ethyl 3,5-dimethylorsellinate
DTXSID60559786
2,4-Dihydroxy-3,5,6-trimethylbenzoic acid ethyl ester

2D Structure

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2D Structure of Ethyl 2,4-dihydroxy-3,5,6-trimethylbenzoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9738 97.38%
Caco-2 + 0.7397 73.97%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.9079 90.79%
OATP2B1 inhibitior - 0.8496 84.96%
OATP1B1 inhibitior + 0.8427 84.27%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.7952 79.52%
P-glycoprotein inhibitior - 0.9095 90.95%
P-glycoprotein substrate - 0.9610 96.10%
CYP3A4 substrate - 0.5902 59.02%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.8718 87.18%
CYP3A4 inhibition - 0.8309 83.09%
CYP2C9 inhibition - 0.7391 73.91%
CYP2C19 inhibition - 0.6248 62.48%
CYP2D6 inhibition - 0.9359 93.59%
CYP1A2 inhibition - 0.5748 57.48%
CYP2C8 inhibition - 0.8654 86.54%
CYP inhibitory promiscuity - 0.6268 62.68%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7260 72.60%
Carcinogenicity (trinary) Non-required 0.7920 79.20%
Eye corrosion - 0.9621 96.21%
Eye irritation + 0.9269 92.69%
Skin irritation - 0.6685 66.85%
Skin corrosion - 0.9674 96.74%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7480 74.80%
Micronuclear - 0.6326 63.26%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.5365 53.65%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.5523 55.23%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity - 0.5794 57.94%
Acute Oral Toxicity (c) III 0.8300 83.00%
Estrogen receptor binding + 0.7267 72.67%
Androgen receptor binding - 0.5805 58.05%
Thyroid receptor binding - 0.6047 60.47%
Glucocorticoid receptor binding - 0.6581 65.81%
Aromatase binding - 0.6947 69.47%
PPAR gamma - 0.8137 81.37%
Honey bee toxicity - 0.9765 97.65%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.6755 67.55%
Fish aquatic toxicity + 0.9661 96.61%

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 89.03% 96.09%
CHEMBL2581 P07339 Cathepsin D 88.28% 98.95%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 88.05% 93.65%
CHEMBL3401 O75469 Pregnane X receptor 83.24% 94.73%
CHEMBL221 P23219 Cyclooxygenase-1 81.24% 90.17%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.29% 94.33%

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.
Calypogeia integristipula
Cirsium brevistylum
Gentiana dahurica
Gymnanthemum amygdalinum
Hylodesmum podocarpum subsp. oxyphyllum
Putterlickia verrucosa

Cross-Links

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PubChem 14394297
NPASS NPC69355