2-Pentenoic acid

Details

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Internal ID f68a95c1-0de7-4b83-9811-eea3f91ad0d9
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Straight chain fatty acids
IUPAC Name (E)-pent-2-enoic acid
SMILES (Canonical) CCC=CC(=O)O
SMILES (Isomeric) CC/C=C/C(=O)O
InChI InChI=1S/C5H8O2/c1-2-3-4-5(6)7/h3-4H,2H2,1H3,(H,6,7)/b4-3+
InChI Key YIYBQIKDCADOSF-ONEGZZNKSA-N
Popularity 135 references in papers

Physical and Chemical Properties

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Molecular Formula C5H8O2
Molecular Weight 100.12 g/mol
Exact Mass 100.052429494 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 1.00
Atomic LogP (AlogP) 1.04
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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13991-37-2
(E)-pent-2-enoic acid
(2E)-pent-2-enoic acid
2-pentenoic acid, (2E)-
(E)-2-pentenoic acid
(2E)-2-Pentenoic acid
Pentenoic acid
MFCD00002704
beta-ethyl acrylic acid
C2H5CH=CHCOOH
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-Pentenoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9913 99.13%
Caco-2 + 0.8777 87.77%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.4398 43.98%
OATP2B1 inhibitior - 0.8539 85.39%
OATP1B1 inhibitior + 0.9348 93.48%
OATP1B3 inhibitior + 0.9281 92.81%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9388 93.88%
P-glycoprotein inhibitior - 0.9849 98.49%
P-glycoprotein substrate - 0.9866 98.66%
CYP3A4 substrate - 0.7839 78.39%
CYP2C9 substrate + 0.6079 60.79%
CYP2D6 substrate - 0.9072 90.72%
CYP3A4 inhibition - 0.9605 96.05%
CYP2C9 inhibition - 0.8771 87.71%
CYP2C19 inhibition - 0.9591 95.91%
CYP2D6 inhibition - 0.9598 95.98%
CYP1A2 inhibition - 0.8857 88.57%
CYP2C8 inhibition - 0.9829 98.29%
CYP inhibitory promiscuity - 0.9353 93.53%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5939 59.39%
Carcinogenicity (trinary) Non-required 0.6311 63.11%
Eye corrosion + 0.9877 98.77%
Eye irritation + 0.9791 97.91%
Skin irritation + 0.9347 93.47%
Skin corrosion + 0.9920 99.20%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8385 83.85%
Micronuclear - 0.9000 90.00%
Hepatotoxicity - 0.5551 55.51%
skin sensitisation + 0.7203 72.03%
Respiratory toxicity - 0.9000 90.00%
Reproductive toxicity - 0.7000 70.00%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity - 0.6086 60.86%
Acute Oral Toxicity (c) III 0.9291 92.91%
Estrogen receptor binding - 0.9634 96.34%
Androgen receptor binding - 0.8845 88.45%
Thyroid receptor binding - 0.9301 93.01%
Glucocorticoid receptor binding - 0.9194 91.94%
Aromatase binding - 0.9171 91.71%
PPAR gamma - 0.8422 84.22%
Honey bee toxicity - 0.9853 98.53%
Biodegradation + 0.8250 82.50%
Crustacea aquatic toxicity - 0.9000 90.00%
Fish aquatic toxicity + 0.7063 70.63%

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 87.50% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 84.69% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.04% 99.17%

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.
There are no matching plants.

Cross-Links

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PubChem 638122
NPASS NPC8270