3-p-Isopropylphenyl-3-methylpropanal

Details

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Internal ID 397853a6-e4e8-4c48-86b0-aa93e5ad6076
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Aromatic monoterpenoids
IUPAC Name 3-(4-propan-2-ylphenyl)butanal
SMILES (Canonical) CC(C)C1=CC=C(C=C1)C(C)CC=O
SMILES (Isomeric) CC(C)C1=CC=C(C=C1)C(C)CC=O
InChI InChI=1S/C13H18O/c1-10(2)12-4-6-13(7-5-12)11(3)8-9-14/h4-7,9-11H,8H2,1-3H3
InChI Key HQQPOVNESMNPNH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H18O
Molecular Weight 190.28 g/mol
Exact Mass 190.135765193 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.50
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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HQQPOVNESMNPNH-UHFFFAOYSA-N
3-p-isopropylphenyl-3-methylpropanal
LS-14230
D91134

2D Structure

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2D Structure of 3-p-Isopropylphenyl-3-methylpropanal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9960 99.60%
Caco-2 + 0.9024 90.24%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.8857 88.57%
Subcellular localzation Mitochondria 0.6232 62.32%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9129 91.29%
OATP1B3 inhibitior + 0.9575 95.75%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8328 83.28%
P-glycoprotein inhibitior - 0.9696 96.96%
P-glycoprotein substrate - 0.9419 94.19%
CYP3A4 substrate - 0.7366 73.66%
CYP2C9 substrate - 0.5824 58.24%
CYP2D6 substrate - 0.7235 72.35%
CYP3A4 inhibition - 0.9313 93.13%
CYP2C9 inhibition - 0.9373 93.73%
CYP2C19 inhibition - 0.9416 94.16%
CYP2D6 inhibition - 0.9050 90.50%
CYP1A2 inhibition - 0.6061 60.61%
CYP2C8 inhibition - 0.9885 98.85%
CYP inhibitory promiscuity - 0.8551 85.51%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5364 53.64%
Carcinogenicity (trinary) Non-required 0.6383 63.83%
Eye corrosion + 0.9182 91.82%
Eye irritation + 0.9082 90.82%
Skin irritation + 0.8289 82.89%
Skin corrosion - 0.8338 83.38%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7143 71.43%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation + 0.9689 96.89%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity - 0.5724 57.24%
Acute Oral Toxicity (c) III 0.9494 94.94%
Estrogen receptor binding - 0.8313 83.13%
Androgen receptor binding - 0.5900 59.00%
Thyroid receptor binding - 0.6543 65.43%
Glucocorticoid receptor binding - 0.7997 79.97%
Aromatase binding - 0.7073 70.73%
PPAR gamma - 0.7877 78.77%
Honey bee toxicity - 0.9135 91.35%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5273 52.73%
Fish aquatic toxicity + 0.8640 86.40%

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
CHEMBL2581 P07339 Cathepsin D 93.08% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.52% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 91.31% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.91% 94.45%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.39% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.32% 91.11%
CHEMBL4208 P20618 Proteasome component C5 85.98% 90.00%
CHEMBL3492 P49721 Proteasome Macropain subunit 83.64% 90.24%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.44% 96.09%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.77% 100.00%

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.
Foeniculum vulgare

Cross-Links

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PubChem 7687
LOTUS LTS0117046
wikiData Q105109954