(E)-3-Methyl-3-pentenoic acid methyl ester

Details

Top
Internal ID 916914e9-cd92-4f80-bb62-111243becbc1
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters > Fatty acid methyl esters
IUPAC Name methyl (E)-3-methylpent-3-enoate
SMILES (Canonical) CC=C(C)CC(=O)OC
SMILES (Isomeric) C/C=C(\C)/CC(=O)OC
InChI InChI=1S/C7H12O2/c1-4-6(2)5-7(8)9-3/h4H,5H2,1-3H3/b6-4+
InChI Key OUARJKDCCMXOEF-GQCTYLIASA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C7H12O2
Molecular Weight 128.17 g/mol
Exact Mass 128.083729621 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 1.70
Atomic LogP (AlogP) 1.52
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

Top
41654-12-0
SCHEMBL6965002
OUARJKDCCMXOEF-GQCTYLIASA-N
methyl trans-3-methylpent-3-enoate
METHYL 3-METHYL-3-PENTENOATE

2D Structure

Top
2D Structure of (E)-3-Methyl-3-pentenoic acid methyl ester

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9951 99.51%
Caco-2 + 0.7233 72.33%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.5031 50.31%
OATP2B1 inhibitior - 0.8629 86.29%
OATP1B1 inhibitior + 0.9274 92.74%
OATP1B3 inhibitior + 0.9233 92.33%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8925 89.25%
P-glycoprotein inhibitior - 0.9757 97.57%
P-glycoprotein substrate - 0.9649 96.49%
CYP3A4 substrate - 0.6855 68.55%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.8708 87.08%
CYP3A4 inhibition - 0.9736 97.36%
CYP2C9 inhibition - 0.9504 95.04%
CYP2C19 inhibition - 0.9240 92.40%
CYP2D6 inhibition - 0.9429 94.29%
CYP1A2 inhibition - 0.9012 90.12%
CYP2C8 inhibition - 0.9855 98.55%
CYP inhibitory promiscuity - 0.8422 84.22%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6257 62.57%
Carcinogenicity (trinary) Non-required 0.6325 63.25%
Eye corrosion + 0.8356 83.56%
Eye irritation + 0.9737 97.37%
Skin irritation + 0.7214 72.14%
Skin corrosion - 0.9749 97.49%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6870 68.70%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.6724 67.24%
skin sensitisation + 0.7423 74.23%
Respiratory toxicity - 0.9222 92.22%
Reproductive toxicity - 0.8333 83.33%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity + 0.6957 69.57%
Acute Oral Toxicity (c) III 0.5344 53.44%
Estrogen receptor binding - 0.9827 98.27%
Androgen receptor binding - 0.9426 94.26%
Thyroid receptor binding - 0.9013 90.13%
Glucocorticoid receptor binding - 0.9293 92.93%
Aromatase binding - 0.9077 90.77%
PPAR gamma - 0.8936 89.36%
Honey bee toxicity - 0.8973 89.73%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 0.8267 82.67%

Targets

Top

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 93.30% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 88.05% 83.82%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.85% 99.17%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 85.14% 94.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.58% 85.14%

Plants that contains it

Top
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.
Nicotiana tabacum

Cross-Links

Top
PubChem 13096522
LOTUS LTS0005686
wikiData Q105199977