2-Ethylpent-3-enoic acid

Details

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Internal ID 6539196e-9643-4ea4-a867-052dee177cdc
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Branched fatty acids > Methyl-branched fatty acids
IUPAC Name 2-ethylpent-3-enoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H12O2/c1-3-5-6(4-2)7(8)9/h3,5-6H,4H2,1-2H3,(H,8,9)
InChI Key RPVFKZTXNWHGGE-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C7H12O2
Molecular Weight 128.17 g/mol
Exact Mass 128.083729621 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 1.70
Atomic LogP (AlogP) 1.67
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Ethylpent-3-enoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9954 99.54%
Caco-2 - 0.5236 52.36%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.5223 52.23%
OATP2B1 inhibitior - 0.8419 84.19%
OATP1B1 inhibitior + 0.8507 85.07%
OATP1B3 inhibitior + 0.9022 90.22%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.8844 88.44%
P-glycoprotein inhibitior - 0.9841 98.41%
P-glycoprotein substrate - 0.9868 98.68%
CYP3A4 substrate - 0.7274 72.74%
CYP2C9 substrate + 0.6453 64.53%
CYP2D6 substrate - 0.8826 88.26%
CYP3A4 inhibition - 0.9653 96.53%
CYP2C9 inhibition - 0.8947 89.47%
CYP2C19 inhibition - 0.9658 96.58%
CYP2D6 inhibition - 0.9523 95.23%
CYP1A2 inhibition - 0.9029 90.29%
CYP2C8 inhibition - 0.9846 98.46%
CYP inhibitory promiscuity - 0.9494 94.94%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6158 61.58%
Carcinogenicity (trinary) Non-required 0.6400 64.00%
Eye corrosion + 0.9475 94.75%
Eye irritation + 0.8496 84.96%
Skin irritation + 0.8438 84.38%
Skin corrosion + 0.9257 92.57%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8163 81.63%
Micronuclear - 0.9200 92.00%
Hepatotoxicity - 0.5551 55.51%
skin sensitisation + 0.8569 85.69%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.7000 70.00%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity - 0.6243 62.43%
Acute Oral Toxicity (c) III 0.9434 94.34%
Estrogen receptor binding - 0.9610 96.10%
Androgen receptor binding - 0.8837 88.37%
Thyroid receptor binding - 0.9529 95.29%
Glucocorticoid receptor binding - 0.9420 94.20%
Aromatase binding - 0.9204 92.04%
PPAR gamma - 0.9200 92.00%
Honey bee toxicity - 0.9550 95.50%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.9300 93.00%
Fish aquatic toxicity + 0.7782 77.82%

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 92.23% 96.09%
CHEMBL2581 P07339 Cathepsin D 86.17% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 85.47% 90.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.39% 96.95%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 80.63% 98.75%

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.
Artemisia judaica

Cross-Links

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PubChem 54141565
LOTUS LTS0113084
wikiData Q105243050