2-Hexenoic acid, (2E)-

Details

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Internal ID ada117d1-e71b-4860-a81f-e27e11f18e28
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Medium-chain fatty acids
IUPAC Name (E)-hex-2-enoic acid
SMILES (Canonical) CCCC=CC(=O)O
SMILES (Isomeric) CCC/C=C/C(=O)O
InChI InChI=1S/C6H10O2/c1-2-3-4-5-6(7)8/h4-5H,2-3H2,1H3,(H,7,8)/b5-4+
InChI Key NIONDZDPPYHYKY-SNAWJCMRSA-N
Popularity 161 references in papers

Physical and Chemical Properties

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Molecular Formula C6H10O2
Molecular Weight 114.14 g/mol
Exact Mass 114.068079557 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.43
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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13419-69-7
trans-Hex-2-enoic acid
(E)-hex-2-enoic acid
hex-2-enoic acid
2-HEXENOIC ACID
2-Hexenoic acid, (2E)-
1191-04-4
(E)-2-Hexenoic acid
Hexenoic acid
(2E)-2-Hexenoic acid
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-Hexenoic acid, (2E)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9879 98.79%
Caco-2 + 0.9283 92.83%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Plasma membrane 0.6509 65.09%
OATP2B1 inhibitior - 0.8583 85.83%
OATP1B1 inhibitior + 0.9153 91.53%
OATP1B3 inhibitior + 0.8804 88.04%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9442 94.42%
P-glycoprotein inhibitior - 0.9869 98.69%
P-glycoprotein substrate - 0.9864 98.64%
CYP3A4 substrate - 0.7656 76.56%
CYP2C9 substrate + 0.6079 60.79%
CYP2D6 substrate - 0.9072 90.72%
CYP3A4 inhibition - 0.9646 96.46%
CYP2C9 inhibition - 0.8830 88.30%
CYP2C19 inhibition - 0.9333 93.33%
CYP2D6 inhibition - 0.9503 95.03%
CYP1A2 inhibition - 0.6162 61.62%
CYP2C8 inhibition - 0.9816 98.16%
CYP inhibitory promiscuity - 0.9234 92.34%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5335 53.35%
Carcinogenicity (trinary) Non-required 0.5775 57.75%
Eye corrosion + 0.9845 98.45%
Eye irritation + 0.9869 98.69%
Skin irritation + 0.8891 88.91%
Skin corrosion + 0.9558 95.58%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7640 76.40%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.5801 58.01%
skin sensitisation + 0.8581 85.81%
Respiratory toxicity - 0.9222 92.22%
Reproductive toxicity - 0.7297 72.97%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity + 0.5236 52.36%
Acute Oral Toxicity (c) III 0.8968 89.68%
Estrogen receptor binding - 0.9640 96.40%
Androgen receptor binding - 0.8600 86.00%
Thyroid receptor binding - 0.9107 91.07%
Glucocorticoid receptor binding - 0.8733 87.33%
Aromatase binding - 0.9290 92.90%
PPAR gamma - 0.8812 88.12%
Honey bee toxicity - 0.9897 98.97%
Biodegradation + 0.9250 92.50%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity + 0.7839 78.39%

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
CHEMBL221 P23219 Cyclooxygenase-1 86.68% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.34% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.09% 96.09%

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.
Arctium lappa
Clibadium eggersii
Deschampsia antarctica
Euphorbia tithymaloides
Vitis vinifera

Cross-Links

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PubChem 5282707
NPASS NPC221250
LOTUS LTS0057174
wikiData Q27159869