2-Ethyl-3-propylacrolein, (Z)-

Details

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Internal ID 5c9df0d9-a391-4efd-bba7-7d2a1de1ff1e
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aldehydes > Medium-chain aldehydes
IUPAC Name (Z)-2-ethylhex-2-enal
SMILES (Canonical) CCCC=C(CC)C=O
SMILES (Isomeric) CCC/C=C(/CC)\C=O
InChI InChI=1S/C8H14O/c1-3-5-6-8(4-2)7-9/h6-7H,3-5H2,1-2H3/b8-6-
InChI Key PYLMCYQHBRSDND-VURMDHGXSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C8H14O
Molecular Weight 126.20 g/mol
Exact Mass 126.104465066 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.32
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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cis-2-Ethyl-2-hexenal
2-Ethyl-3-propylacrolein, (Z)-
2-Hexenal, 2-ethyl-, (2Z)-
UNII-0Y7M27M05R
0Y7M27M05R
88288-45-3
(Z)-2-Ethyl-2-hexenal
(Z)-2-ethyl-3-propylacrolein
645-62-5
Hexenal, 2-ethyl-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2-Ethyl-3-propylacrolein, (Z)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9933 99.33%
Caco-2 + 0.9664 96.64%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Plasma membrane 0.2967 29.67%
OATP2B1 inhibitior - 0.8438 84.38%
OATP1B1 inhibitior + 0.9123 91.23%
OATP1B3 inhibitior + 0.9326 93.26%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8904 89.04%
P-glycoprotein inhibitior - 0.9869 98.69%
P-glycoprotein substrate - 0.9660 96.60%
CYP3A4 substrate - 0.7075 70.75%
CYP2C9 substrate - 0.5918 59.18%
CYP2D6 substrate - 0.8311 83.11%
CYP3A4 inhibition - 0.9712 97.12%
CYP2C9 inhibition - 0.9350 93.50%
CYP2C19 inhibition - 0.9518 95.18%
CYP2D6 inhibition - 0.9501 95.01%
CYP1A2 inhibition - 0.5774 57.74%
CYP2C8 inhibition - 0.9481 94.81%
CYP inhibitory promiscuity - 0.6210 62.10%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5200 52.00%
Carcinogenicity (trinary) Non-required 0.5044 50.44%
Eye corrosion + 0.8903 89.03%
Eye irritation + 0.9896 98.96%
Skin irritation + 0.7034 70.34%
Skin corrosion - 0.9613 96.13%
Ames mutagenesis - 0.9600 96.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6308 63.08%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5551 55.51%
skin sensitisation + 0.9702 97.02%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.9111 91.11%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.6063 60.63%
Acute Oral Toxicity (c) III 0.8584 85.84%
Estrogen receptor binding - 0.9473 94.73%
Androgen receptor binding - 0.9040 90.40%
Thyroid receptor binding - 0.8598 85.98%
Glucocorticoid receptor binding - 0.9218 92.18%
Aromatase binding - 0.8669 86.69%
PPAR gamma - 0.9171 91.71%
Honey bee toxicity - 0.9773 97.73%
Biodegradation + 0.8000 80.00%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.9717 97.17%

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
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 84.12% 89.34%
CHEMBL3401 O75469 Pregnane X receptor 80.62% 94.73%

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.
Cinnamomum aromaticum
Conioselinum anthriscoides
Ligusticum officinale

Cross-Links

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PubChem 10997035
NPASS NPC13212