2-Propyl-2-heptenal

Details

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Internal ID e934abf3-a711-442d-83d7-47f71f4ba854
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aldehydes > Medium-chain aldehydes
IUPAC Name 2-propylhept-2-enal
SMILES (Canonical) CCCCC=C(CCC)C=O
SMILES (Isomeric) CCCCC=C(CCC)C=O
InChI InChI=1S/C10H18O/c1-3-5-6-8-10(9-11)7-4-2/h8-9H,3-7H2,1-2H3
InChI Key GADNZGQWPNTMCH-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C10H18O
Molecular Weight 154.25 g/mol
Exact Mass 154.135765193 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.10
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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2-Propyl-2-heptenal
34880-43-8
2-Propylheptenal
(Z)-2-propylhept-2-enal
2-n-propyl-2-heptenal
GADNZGQWPNTMCH-UHFFFAOYSA-N
AKOS030239842

2D Structure

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2D Structure of 2-Propyl-2-heptenal

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 + 0.9779 97.79%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Plasma membrane 0.2960 29.60%
OATP2B1 inhibitior - 0.8468 84.68%
OATP1B1 inhibitior + 0.8590 85.90%
OATP1B3 inhibitior + 0.9358 93.58%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8525 85.25%
P-glycoprotein inhibitior - 0.9725 97.25%
P-glycoprotein substrate - 0.8996 89.96%
CYP3A4 substrate - 0.6645 66.45%
CYP2C9 substrate - 0.5918 59.18%
CYP2D6 substrate - 0.8311 83.11%
CYP3A4 inhibition - 0.9690 96.90%
CYP2C9 inhibition - 0.9343 93.43%
CYP2C19 inhibition - 0.9400 94.00%
CYP2D6 inhibition - 0.9492 94.92%
CYP1A2 inhibition + 0.5181 51.81%
CYP2C8 inhibition - 0.9129 91.29%
CYP inhibitory promiscuity - 0.6297 62.97%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5500 55.00%
Carcinogenicity (trinary) Non-required 0.5987 59.87%
Eye corrosion + 0.9246 92.46%
Eye irritation + 0.9835 98.35%
Skin irritation + 0.7566 75.66%
Skin corrosion - 0.8816 88.16%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6050 60.50%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6449 64.49%
skin sensitisation + 0.9576 95.76%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity - 0.8889 88.89%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity + 0.5688 56.88%
Acute Oral Toxicity (c) III 0.8944 89.44%
Estrogen receptor binding - 0.9449 94.49%
Androgen receptor binding - 0.8503 85.03%
Thyroid receptor binding - 0.7962 79.62%
Glucocorticoid receptor binding - 0.8760 87.60%
Aromatase binding - 0.8961 89.61%
PPAR gamma - 0.8322 83.22%
Honey bee toxicity - 0.9897 98.97%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9848 98.48%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 91.46% 92.08%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.35% 99.17%
CHEMBL2581 P07339 Cathepsin D 84.52% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.69% 95.56%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 83.62% 85.94%
CHEMBL3401 O75469 Pregnane X receptor 82.32% 94.73%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 81.31% 97.29%

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.
Coleus paniculatus

Cross-Links

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PubChem 118745
LOTUS LTS0039230
wikiData Q81994538