2-Ethyl-2-methylbutanoate

Details

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Internal ID b4cdb845-5c75-453a-b731-ba19bbbe9752
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Branched fatty acids > Methyl-branched fatty acids
IUPAC Name 2-ethyl-2-methylbutanoate
SMILES (Canonical) CCC(C)(CC)C(=O)[O-]
SMILES (Isomeric) CCC(C)(CC)C(=O)[O-]
InChI InChI=1S/C7H14O2/c1-4-7(3,5-2)6(8)9/h4-5H2,1-3H3,(H,8,9)/p-1
InChI Key LHJPKLWGGMAUAN-UHFFFAOYSA-M
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C7H13O2-
Molecular Weight 129.18 g/mol
Exact Mass 129.091554653 g/mol
Topological Polar Surface Area (TPSA) 40.10 Ų
XlogP 2.60
Atomic LogP (AlogP) 0.56
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Ethyl-2-methylbutanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9827 98.27%
Caco-2 + 0.9132 91.32%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.5799 57.99%
OATP2B1 inhibitior - 0.8442 84.42%
OATP1B1 inhibitior + 0.9392 93.92%
OATP1B3 inhibitior + 0.9402 94.02%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9015 90.15%
P-glycoprotein inhibitior - 0.9913 99.13%
P-glycoprotein substrate - 0.9825 98.25%
CYP3A4 substrate - 0.7098 70.98%
CYP2C9 substrate - 0.5969 59.69%
CYP2D6 substrate - 0.8688 86.88%
CYP3A4 inhibition - 0.9502 95.02%
CYP2C9 inhibition - 0.8935 89.35%
CYP2C19 inhibition - 0.9429 94.29%
CYP2D6 inhibition - 0.9139 91.39%
CYP1A2 inhibition - 0.7949 79.49%
CYP2C8 inhibition - 0.9860 98.60%
CYP inhibitory promiscuity - 0.9456 94.56%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6474 64.74%
Carcinogenicity (trinary) Non-required 0.6097 60.97%
Eye corrosion + 0.9798 97.98%
Eye irritation + 0.9675 96.75%
Skin irritation + 0.8469 84.69%
Skin corrosion - 0.5166 51.66%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8196 81.96%
Micronuclear - 0.9000 90.00%
Hepatotoxicity + 0.7000 70.00%
skin sensitisation - 0.5646 56.46%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.7333 73.33%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.7507 75.07%
Estrogen receptor binding - 0.9360 93.60%
Androgen receptor binding - 0.8740 87.40%
Thyroid receptor binding - 0.8806 88.06%
Glucocorticoid receptor binding - 0.9531 95.31%
Aromatase binding - 0.9024 90.24%
PPAR gamma - 0.8921 89.21%
Honey bee toxicity - 0.9434 94.34%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.7700 77.00%
Fish aquatic toxicity + 0.8696 86.96%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.41% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.09% 96.09%
CHEMBL2581 P07339 Cathepsin D 85.28% 98.95%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.92% 96.95%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 81.35% 100.00%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.14% 89.34%

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.
Arnebia euchroma
Arnebia guttata
Lithospermum erythrorhizon

Cross-Links

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PubChem 21434475
NPASS NPC164359