Acrolein

Details

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Internal ID 5784c5bd-e2be-4936-a3bd-5a03607e7583
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Alpha,beta-unsaturated aldehydes > Enals
IUPAC Name prop-2-enal
SMILES (Canonical) C=CC=O
SMILES (Isomeric) C=CC=O
InChI InChI=1S/C3H4O/c1-2-3-4/h2-3H,1H2
InChI Key HGINCPLSRVDWNT-UHFFFAOYSA-N
Popularity 14,035 references in papers

Physical and Chemical Properties

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Molecular Formula C3H4O
Molecular Weight 56.06 g/mol
Exact Mass 56.026214747 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 0.00
Atomic LogP (AlogP) 0.37
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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Acrylaldehyde
2-Propenal
107-02-8
Propenal
Acrylic aldehyde
prop-2-enal
Aqualin
Allyl aldehyde
Magnacide H
Acraldehyde
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Acrolein

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9921 99.21%
Caco-2 + 0.7750 77.50%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.3390 33.90%
OATP2B1 inhibitior - 0.8780 87.80%
OATP1B1 inhibitior + 0.9595 95.95%
OATP1B3 inhibitior + 0.9574 95.74%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9381 93.81%
P-glycoprotein inhibitior - 0.9882 98.82%
P-glycoprotein substrate - 0.9972 99.72%
CYP3A4 substrate - 0.7853 78.53%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8198 81.98%
CYP3A4 inhibition - 0.9668 96.68%
CYP2C9 inhibition - 0.9497 94.97%
CYP2C19 inhibition - 0.9209 92.09%
CYP2D6 inhibition - 0.9709 97.09%
CYP1A2 inhibition - 0.8095 80.95%
CYP2C8 inhibition - 0.9942 99.42%
CYP inhibitory promiscuity - 0.8891 88.91%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.7583 75.83%
Carcinogenicity (trinary) Non-required 0.6616 66.16%
Eye corrosion + 1.0000 100.00%
Eye irritation + 0.9868 98.68%
Skin irritation + 0.9170 91.70%
Skin corrosion + 0.9671 96.71%
Ames mutagenesis + 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7925 79.25%
Micronuclear + 0.6400 64.00%
Hepatotoxicity + 0.8625 86.25%
skin sensitisation + 0.9686 96.86%
Respiratory toxicity - 0.9000 90.00%
Reproductive toxicity - 0.9222 92.22%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.7448 74.48%
Acute Oral Toxicity (c) I 0.5145 51.45%
Estrogen receptor binding - 0.8557 85.57%
Androgen receptor binding - 0.9441 94.41%
Thyroid receptor binding - 0.8134 81.34%
Glucocorticoid receptor binding - 0.7754 77.54%
Aromatase binding - 0.8902 89.02%
PPAR gamma - 0.8139 81.39%
Honey bee toxicity + 0.5432 54.32%
Biodegradation + 0.8250 82.50%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.7191 71.91%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL3577 P00352 Aldehyde dehydrogenase 1A1 22.4 nM
22.4 nM
Potency
Potency
via CMAUP
via Super-PRED
CHEMBL1963 P16473 Thyroid stimulating hormone receptor 39810.7 nM
39810.7 nM
Potency
Potency
via CMAUP
via CMAUP
CHEMBL6007 O75762 Transient receptor potential cation channel subfamily A member 1 5000 nM
800 nM
EC50
EC50
PMID: 17237762
PMID: 20356305

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.41% 95.56%

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.
Aloe africana
Aloe ferox
Aloe spicata
Aloe vera
Camellia saluenensis
Zanthoxylum bungeanum
Zanthoxylum schinifolium

Cross-Links

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PubChem 7847
NPASS NPC235797
ChEMBL CHEMBL721