Isobutyl isovalerate

Details

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Internal ID 5ed3126c-6333-4e65-b870-26493a484ed5
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters
IUPAC Name 2-methylpropyl 3-methylbutanoate
SMILES (Canonical) CC(C)CC(=O)OCC(C)C
SMILES (Isomeric) CC(C)CC(=O)OCC(C)C
InChI InChI=1S/C9H18O2/c1-7(2)5-9(10)11-6-8(3)4/h7-8H,5-6H2,1-4H3
InChI Key KEBDNKNVCHQIJU-UHFFFAOYSA-N
Popularity 23 references in papers

Physical and Chemical Properties

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Molecular Formula C9H18O2
Molecular Weight 158.24 g/mol
Exact Mass 158.130679813 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.23
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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589-59-3
2-Methylpropyl 3-methylbutanoate
Isovaleric acid, isobutyl ester
Butanoic acid, 3-methyl-, 2-methylpropyl ester
2-Methylpropyl 3-methylbutyrate
2-Methylpropyl isovalerate
Isobutyl isopentanoate
Isobutyl 3-methylpropanoate
Isobutylisovalerate
Isovaleric Acid Isobutyl Ester
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Isobutyl isovalerate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9934 99.34%
Caco-2 + 0.7689 76.89%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.7987 79.87%
OATP2B1 inhibitior - 0.8483 84.83%
OATP1B1 inhibitior + 0.9433 94.33%
OATP1B3 inhibitior + 0.9455 94.55%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9122 91.22%
P-glycoprotein inhibitior - 0.9564 95.64%
P-glycoprotein substrate - 0.9738 97.38%
CYP3A4 substrate - 0.6642 66.42%
CYP2C9 substrate + 0.5942 59.42%
CYP2D6 substrate - 0.8718 87.18%
CYP3A4 inhibition - 0.9680 96.80%
CYP2C9 inhibition - 0.9326 93.26%
CYP2C19 inhibition - 0.9390 93.90%
CYP2D6 inhibition - 0.9512 95.12%
CYP1A2 inhibition - 0.8034 80.34%
CYP2C8 inhibition - 0.9935 99.35%
CYP inhibitory promiscuity - 0.9006 90.06%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5583 55.83%
Carcinogenicity (trinary) Warning 0.5184 51.84%
Eye corrosion + 0.9925 99.25%
Eye irritation + 0.9666 96.66%
Skin irritation + 0.5288 52.88%
Skin corrosion - 0.9580 95.80%
Ames mutagenesis - 0.9900 99.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7436 74.36%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation + 0.6798 67.98%
Respiratory toxicity - 0.8778 87.78%
Reproductive toxicity - 0.9444 94.44%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity + 0.5131 51.31%
Acute Oral Toxicity (c) III 0.8079 80.79%
Estrogen receptor binding - 0.8914 89.14%
Androgen receptor binding - 0.8662 86.62%
Thyroid receptor binding - 0.9068 90.68%
Glucocorticoid receptor binding - 0.8649 86.49%
Aromatase binding - 0.8335 83.35%
PPAR gamma - 0.9309 93.09%
Honey bee toxicity - 0.9414 94.14%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.7655 76.55%
Fish aquatic toxicity + 0.8056 80.56%

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 94.23% 96.09%
CHEMBL2581 P07339 Cathepsin D 85.95% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.81% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.50% 96.95%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 83.44% 100.00%
CHEMBL4040 P28482 MAP kinase ERK2 82.37% 83.82%

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.
Eucalyptus dolichorhyncha
Eucalyptus leucoxylon
Hippophae rhamnoides
Humulus lupulus

Cross-Links

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PubChem 11514
NPASS NPC165620
LOTUS LTS0238308
wikiData Q27161264