4-(2-Hydroxyethyl)-3,5-dimethyl-2-(2-methyl-3-oxoprop-1-enyl)benzaldehyde

Details

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Internal ID 494197a3-0ff1-4408-b85d-6d13a7338d5c
Taxonomy Phenylpropanoids and polyketides > Cinnamaldehydes
IUPAC Name 4-(2-hydroxyethyl)-3,5-dimethyl-2-(2-methyl-3-oxoprop-1-enyl)benzaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H18O3/c1-10(8-17)6-15-12(3)14(4-5-16)11(2)7-13(15)9-18/h6-9,16H,4-5H2,1-3H3
InChI Key QQQDFWJDGZDCQP-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C15H18O3
Molecular Weight 246.30 g/mol
Exact Mass 246.125594432 g/mol
Topological Polar Surface Area (TPSA) 54.40 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.25
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-(2-Hydroxyethyl)-3,5-dimethyl-2-(2-methyl-3-oxoprop-1-enyl)benzaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9953 99.53%
Caco-2 + 0.8907 89.07%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.8052 80.52%
OATP2B1 inhibitior - 0.8577 85.77%
OATP1B1 inhibitior + 0.7359 73.59%
OATP1B3 inhibitior + 0.9308 93.08%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.6425 64.25%
P-glycoprotein inhibitior - 0.9682 96.82%
P-glycoprotein substrate - 0.8364 83.64%
CYP3A4 substrate - 0.5562 55.62%
CYP2C9 substrate - 0.6033 60.33%
CYP2D6 substrate - 0.8170 81.70%
CYP3A4 inhibition - 0.5546 55.46%
CYP2C9 inhibition - 0.8087 80.87%
CYP2C19 inhibition - 0.6904 69.04%
CYP2D6 inhibition - 0.7783 77.83%
CYP1A2 inhibition - 0.5346 53.46%
CYP2C8 inhibition - 0.8542 85.42%
CYP inhibitory promiscuity - 0.8220 82.20%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.6846 68.46%
Carcinogenicity (trinary) Non-required 0.7375 73.75%
Eye corrosion - 0.9636 96.36%
Eye irritation - 0.6889 68.89%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9321 93.21%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4911 49.11%
Micronuclear - 0.8900 89.00%
Hepatotoxicity - 0.5175 51.75%
skin sensitisation + 0.7300 73.00%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity + 0.6966 69.66%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity + 0.5100 51.00%
Acute Oral Toxicity (c) III 0.7976 79.76%
Estrogen receptor binding - 0.5528 55.28%
Androgen receptor binding - 0.7462 74.62%
Thyroid receptor binding - 0.5981 59.81%
Glucocorticoid receptor binding - 0.6106 61.06%
Aromatase binding - 0.6206 62.06%
PPAR gamma + 0.7297 72.97%
Honey bee toxicity - 0.9172 91.72%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.8200 82.00%
Fish aquatic toxicity + 0.9284 92.84%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.82% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 93.71% 94.73%
CHEMBL2581 P07339 Cathepsin D 91.78% 98.95%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 91.63% 98.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.68% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.27% 91.11%
CHEMBL2664 P23526 Adenosylhomocysteinase 80.84% 86.67%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.69% 96.00%

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.
There are no matching plants.

Cross-Links

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PubChem 162845062
LOTUS LTS0039123
wikiData Q105225989