(4R)-4-(4-methylphenyl)pentanal

Details

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Internal ID 55e2e2e7-55c6-454d-b728-d0f4309d4abd
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Aromatic monoterpenoids
IUPAC Name (4R)-4-(4-methylphenyl)pentanal
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H16O/c1-10-5-7-12(8-6-10)11(2)4-3-9-13/h5-9,11H,3-4H2,1-2H3/t11-/m1/s1
InChI Key XPYKOJLMORBJQP-LLVKDONJSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C12H16O
Molecular Weight 176.25 g/mol
Exact Mass 176.120115130 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.70
Atomic LogP (AlogP) 3.08
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4R)-4-(4-methylphenyl)pentanal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9968 99.68%
Caco-2 + 0.9479 94.79%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Mitochondria 0.5003 50.03%
OATP2B1 inhibitior - 0.8652 86.52%
OATP1B1 inhibitior + 0.9204 92.04%
OATP1B3 inhibitior + 0.9546 95.46%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.7799 77.99%
P-glycoprotein inhibitior - 0.9870 98.70%
P-glycoprotein substrate - 0.9238 92.38%
CYP3A4 substrate - 0.6973 69.73%
CYP2C9 substrate - 0.5824 58.24%
CYP2D6 substrate - 0.7235 72.35%
CYP3A4 inhibition - 0.9536 95.36%
CYP2C9 inhibition - 0.9649 96.49%
CYP2C19 inhibition - 0.9274 92.74%
CYP2D6 inhibition - 0.9351 93.51%
CYP1A2 inhibition + 0.5276 52.76%
CYP2C8 inhibition - 0.9952 99.52%
CYP inhibitory promiscuity - 0.8876 88.76%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Non-required 0.7329 73.29%
Eye corrosion + 0.9276 92.76%
Eye irritation + 0.8504 85.04%
Skin irritation + 0.8901 89.01%
Skin corrosion - 0.8373 83.73%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation + 0.9329 93.29%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.6889 68.89%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity + 0.5524 55.24%
Acute Oral Toxicity (c) III 0.9284 92.84%
Estrogen receptor binding - 0.8820 88.20%
Androgen receptor binding - 0.7286 72.86%
Thyroid receptor binding - 0.7769 77.69%
Glucocorticoid receptor binding - 0.8202 82.02%
Aromatase binding - 0.7542 75.42%
PPAR gamma - 0.7990 79.90%
Honey bee toxicity - 0.9069 90.69%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.8449 84.49%

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 95.97% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 94.07% 94.73%
CHEMBL2581 P07339 Cathepsin D 93.81% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 88.20% 96.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.62% 93.56%
CHEMBL1907 P15144 Aminopeptidase N 83.41% 93.31%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.96% 96.09%
CHEMBL4581 P52732 Kinesin-like protein 1 81.54% 93.18%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.02% 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.
Santalum album

Cross-Links

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PubChem 15592387
LOTUS LTS0263116
wikiData Q105339099