Butyloctenal

Details

Top
Internal ID 7c806398-7c49-4ca9-9544-80d2843709e1
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aldehydes > Medium-chain aldehydes
IUPAC Name 2-butyloct-2-enal
SMILES (Canonical) CCCCCC=C(CCCC)C=O
SMILES (Isomeric) CCCCCC=C(CCCC)C=O
InChI InChI=1S/C12H22O/c1-3-5-7-8-10-12(11-13)9-6-4-2/h10-11H,3-9H2,1-2H3
InChI Key LYGMPIZYNJGJKP-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

Top
Molecular Formula C12H22O
Molecular Weight 182.30 g/mol
Exact Mass 182.167065321 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 4.50
Atomic LogP (AlogP) 3.88
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 8

Synonyms

Top
13019-16-4
2-BUTYL-2-OCTENAL
UNII-82P740211E
SCHEMBL730613
DTXSID20864348
LYGMPIZYNJGJKP-UHFFFAOYSA-N
AKOS030227977

2D Structure

Top
2D Structure of Butyloctenal

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9950 99.50%
Caco-2 + 0.9801 98.01%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Lysosomes 0.3038 30.38%
OATP2B1 inhibitior - 0.8460 84.60%
OATP1B1 inhibitior + 0.7959 79.59%
OATP1B3 inhibitior + 0.9267 92.67%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.7211 72.11%
P-glycoprotein inhibitior - 0.9635 96.35%
P-glycoprotein substrate - 0.9391 93.91%
CYP3A4 substrate - 0.6481 64.81%
CYP2C9 substrate - 0.5918 59.18%
CYP2D6 substrate - 0.8311 83.11%
CYP3A4 inhibition - 0.9778 97.78%
CYP2C9 inhibition - 0.9349 93.49%
CYP2C19 inhibition - 0.9464 94.64%
CYP2D6 inhibition - 0.9487 94.87%
CYP1A2 inhibition + 0.5225 52.25%
CYP2C8 inhibition - 0.8753 87.53%
CYP inhibitory promiscuity - 0.6469 64.69%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5700 57.00%
Carcinogenicity (trinary) Non-required 0.5861 58.61%
Eye corrosion + 0.8917 89.17%
Eye irritation + 0.9793 97.93%
Skin irritation + 0.8111 81.11%
Skin corrosion - 0.8916 89.16%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5946 59.46%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5199 51.99%
skin sensitisation + 0.9652 96.52%
Respiratory toxicity - 0.8444 84.44%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity + 0.4691 46.91%
Acute Oral Toxicity (c) III 0.8186 81.86%
Estrogen receptor binding - 0.7993 79.93%
Androgen receptor binding - 0.8058 80.58%
Thyroid receptor binding - 0.6465 64.65%
Glucocorticoid receptor binding - 0.8073 80.73%
Aromatase binding - 0.8009 80.09%
PPAR gamma - 0.6808 68.08%
Honey bee toxicity - 0.9898 98.98%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity + 0.6047 60.47%
Fish aquatic toxicity + 0.9876 98.76%

Targets

Top

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 93.04% 92.08%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.23% 99.17%
CHEMBL230 P35354 Cyclooxygenase-2 88.24% 89.63%
CHEMBL2581 P07339 Cathepsin D 87.25% 98.95%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 86.28% 97.29%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 84.79% 85.94%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 83.72% 89.34%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.71% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 83.50% 94.73%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 83.44% 92.86%

Plants that contains it

Top
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.
Pyrus pyrifolia
Vincetoxicum glaucescens
Vincetoxicum stauntonii

Cross-Links

Top
PubChem 25610
NPASS NPC222591
LOTUS LTS0183014
wikiData Q72514452