Ethyl 3,3-dimethylacrylate

Details

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Internal ID 65d49851-ad26-4c42-8be8-db85bae9262a
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters
IUPAC Name ethyl 3-methylbut-2-enoate
SMILES (Canonical) CCOC(=O)C=C(C)C
SMILES (Isomeric) CCOC(=O)C=C(C)C
InChI InChI=1S/C7H12O2/c1-4-9-7(8)5-6(2)3/h5H,4H2,1-3H3
InChI Key UTXVCHVLDOLVPC-UHFFFAOYSA-N
Popularity 45 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) 26.30 Ų
XlogP 1.90
Atomic LogP (AlogP) 1.52
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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638-10-8
Ethyl 3-methylbut-2-enoate
Ethyl 3-methylcrotonate
Ethyl 3-methyl-2-butenoate
Ethyl senecioate
Ethyl isobutenoate
3,3-Dimethylacrylic acid ethyl ester
2-Butenoic acid, 3-methyl-, ethyl ester
Ethyl isopropylideneacetate
Ethyl-Beta,Beta-Dimethyl Acrylate
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Ethyl 3,3-dimethylacrylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9973 99.73%
Caco-2 + 0.8742 87.42%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7065 70.65%
OATP2B1 inhibitior - 0.8590 85.90%
OATP1B1 inhibitior + 0.9630 96.30%
OATP1B3 inhibitior + 0.9516 95.16%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8621 86.21%
P-glycoprotein inhibitior - 0.9857 98.57%
P-glycoprotein substrate - 0.9884 98.84%
CYP3A4 substrate - 0.6283 62.83%
CYP2C9 substrate + 0.7980 79.80%
CYP2D6 substrate - 0.9177 91.77%
CYP3A4 inhibition - 0.9633 96.33%
CYP2C9 inhibition - 0.8900 89.00%
CYP2C19 inhibition - 0.9117 91.17%
CYP2D6 inhibition - 0.9378 93.78%
CYP1A2 inhibition - 0.8451 84.51%
CYP2C8 inhibition - 0.9718 97.18%
CYP inhibitory promiscuity - 0.5661 56.61%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5674 56.74%
Carcinogenicity (trinary) Non-required 0.4958 49.58%
Eye corrosion + 0.8837 88.37%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.8006 80.06%
Skin corrosion - 0.8462 84.62%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7634 76.34%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5026 50.26%
skin sensitisation + 0.7717 77.17%
Respiratory toxicity - 0.8667 86.67%
Reproductive toxicity - 0.9000 90.00%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity + 0.6279 62.79%
Acute Oral Toxicity (c) III 0.6260 62.60%
Estrogen receptor binding - 0.9658 96.58%
Androgen receptor binding - 0.8375 83.75%
Thyroid receptor binding - 0.9104 91.04%
Glucocorticoid receptor binding - 0.8993 89.93%
Aromatase binding - 0.8908 89.08%
PPAR gamma - 0.9072 90.72%
Honey bee toxicity - 0.9150 91.50%
Biodegradation + 0.8250 82.50%
Crustacea aquatic toxicity - 0.8055 80.55%
Fish aquatic toxicity + 0.9004 90.04%

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
CHEMBL4040 P28482 MAP kinase ERK2 97.42% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.93% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 91.49% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 89.63% 97.21%
CHEMBL3401 O75469 Pregnane X receptor 88.15% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.58% 99.17%
CHEMBL2581 P07339 Cathepsin D 81.59% 98.95%

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.
Hippophae rhamnoides
Lithospermum erythrorhizon
Vaccinium angustifolium

Cross-Links

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PubChem 12516
NPASS NPC203863
LOTUS LTS0017512
wikiData Q27255837