Butanoic acid, 3-methyl-, 3-methyl-2-butenyl ester

Details

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Internal ID 389859fd-d9da-49a0-b8c9-03c52f3a0e71
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters
IUPAC Name 3-methylbut-2-enyl 3-methylbutanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H18O2/c1-8(2)5-6-12-10(11)7-9(3)4/h5,9H,6-7H2,1-4H3
InChI Key SXWCTQGESRWYMK-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C10H18O2
Molecular Weight 170.25 g/mol
Exact Mass 170.130679813 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.54
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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Butanoic acid, 3-methyl-, 3-methyl-2-butenyl ester
Methylbutenyl isovalerate
DTXSID00431815
SXWCTQGESRWYMK-UHFFFAOYSA-N
3-methyl-2-butenyl 3-methylbutanoate
3-METHYLBUT-2-EN-1-YL 3-METHYLBUTANOATE

2D Structure

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2D Structure of Butanoic acid, 3-methyl-, 3-methyl-2-butenyl ester

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9959 99.59%
Caco-2 + 0.8716 87.16%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7078 70.78%
OATP2B1 inhibitior - 0.8584 85.84%
OATP1B1 inhibitior + 0.9475 94.75%
OATP1B3 inhibitior + 0.9268 92.68%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8825 88.25%
P-glycoprotein inhibitior - 0.9715 97.15%
P-glycoprotein substrate - 0.9620 96.20%
CYP3A4 substrate - 0.6254 62.54%
CYP2C9 substrate + 0.5955 59.55%
CYP2D6 substrate - 0.8761 87.61%
CYP3A4 inhibition - 0.9506 95.06%
CYP2C9 inhibition - 0.9199 91.99%
CYP2C19 inhibition - 0.8826 88.26%
CYP2D6 inhibition - 0.9345 93.45%
CYP1A2 inhibition - 0.8031 80.31%
CYP2C8 inhibition - 0.9860 98.60%
CYP inhibitory promiscuity - 0.7570 75.70%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5083 50.83%
Carcinogenicity (trinary) Non-required 0.4749 47.49%
Eye corrosion + 0.8735 87.35%
Eye irritation + 0.9840 98.40%
Skin irritation + 0.7563 75.63%
Skin corrosion - 0.9475 94.75%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7150 71.50%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.6150 61.50%
skin sensitisation + 0.6743 67.43%
Respiratory toxicity - 0.9000 90.00%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.7005 70.05%
Acute Oral Toxicity (c) III 0.7460 74.60%
Estrogen receptor binding - 0.9174 91.74%
Androgen receptor binding - 0.8910 89.10%
Thyroid receptor binding - 0.8965 89.65%
Glucocorticoid receptor binding - 0.8698 86.98%
Aromatase binding - 0.7940 79.40%
PPAR gamma - 0.9430 94.30%
Honey bee toxicity - 0.8816 88.16%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.8455 84.55%
Fish aquatic toxicity + 0.9711 97.11%

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%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.87% 94.45%
CHEMBL2581 P07339 Cathepsin D 87.21% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.16% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.83% 96.95%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 81.17% 100.00%

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.
Callitropsis nootkatensis

Cross-Links

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PubChem 9855586
LOTUS LTS0273892
wikiData Q82245794