Ethylacrolein

Details

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Internal ID 5018e88b-f2e6-4588-9682-7d8c9df33248
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Alpha,beta-unsaturated aldehydes > Enals
IUPAC Name 2-methylidenebutanal
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C5H8O/c1-3-5(2)4-6/h4H,2-3H2,1H3
InChI Key GMLDCZYTIPCVMO-UHFFFAOYSA-N
Popularity 56 references in papers

Physical and Chemical Properties

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Molecular Formula C5H8O
Molecular Weight 84.12 g/mol
Exact Mass 84.057514874 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.15
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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922-63-4
2-Methylenebutanal
Ethacrolein
alpha-Ethylacrolein
Ethylacrolein
DTXSID1029205
RefChem:111231
DTXCID309205
213-079-3
2-methylidenebutanal
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Ethylacrolein

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9943 99.43%
Caco-2 + 0.8433 84.33%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.3449 34.49%
OATP2B1 inhibitior - 0.8698 86.98%
OATP1B1 inhibitior + 0.9249 92.49%
OATP1B3 inhibitior + 0.9476 94.76%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9272 92.72%
P-glycoprotein inhibitior - 0.9841 98.41%
P-glycoprotein substrate - 0.9837 98.37%
CYP3A4 substrate - 0.7286 72.86%
CYP2C9 substrate - 0.7970 79.70%
CYP2D6 substrate - 0.7716 77.16%
CYP3A4 inhibition - 0.9551 95.51%
CYP2C9 inhibition - 0.9044 90.44%
CYP2C19 inhibition - 0.8842 88.42%
CYP2D6 inhibition - 0.9441 94.41%
CYP1A2 inhibition - 0.7745 77.45%
CYP2C8 inhibition - 0.9811 98.11%
CYP inhibitory promiscuity - 0.6474 64.74%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.7000 70.00%
Carcinogenicity (trinary) Non-required 0.5527 55.27%
Eye corrosion + 0.9869 98.69%
Eye irritation + 0.9917 99.17%
Skin irritation + 0.8273 82.73%
Skin corrosion + 0.8687 86.87%
Ames mutagenesis - 0.5654 56.54%
Human Ether-a-go-go-Related Gene inhibition - 0.7770 77.70%
Micronuclear - 0.8000 80.00%
Hepatotoxicity - 0.5051 50.51%
skin sensitisation + 0.9614 96.14%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.9667 96.67%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.5226 52.26%
Acute Oral Toxicity (c) III 0.4989 49.89%
Estrogen receptor binding - 0.9310 93.10%
Androgen receptor binding - 0.8966 89.66%
Thyroid receptor binding - 0.8577 85.77%
Glucocorticoid receptor binding - 0.8914 89.14%
Aromatase binding - 0.7901 79.01%
PPAR gamma - 0.8604 86.04%
Honey bee toxicity - 0.9372 93.72%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity - 0.8600 86.00%
Fish aquatic toxicity + 0.8594 85.94%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.94% 96.09%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.02% 89.34%
CHEMBL2581 P07339 Cathepsin D 80.80% 98.95%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 70203
NPASS NPC222599