Isopropyl isovalerate

Details

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Internal ID af2fcf8d-0584-4a38-ac6f-7739916cdebf
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters
IUPAC Name propan-2-yl 3-methylbutanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H16O2/c1-6(2)5-8(9)10-7(3)4/h6-7H,5H2,1-4H3
InChI Key ZOIRKXLFEHOVER-UHFFFAOYSA-N
Popularity 17 references in papers

Physical and Chemical Properties

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Molecular Formula C8H16O2
Molecular Weight 144.21 g/mol
Exact Mass 144.115029749 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 2.20
Atomic LogP (AlogP) 1.98
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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Isopropyl 3-methylbutanoate
32665-23-9
propan-2-yl 3-methylbutanoate
Isopropyl isopentanoate
Isopropyl isovalianate
iso-Propyl iso-valerate
1-Methylethyl 3-methylbutanoate
Butanoic acid, 3-methyl-, 1-methylethyl ester
Isopropyl 3-methylbutyrate
FEMA No. 2961
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Isopropyl isovalerate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9916 99.16%
Caco-2 + 0.7180 71.80%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7510 75.10%
OATP2B1 inhibitior - 0.8599 85.99%
OATP1B1 inhibitior + 0.9255 92.55%
OATP1B3 inhibitior + 0.9426 94.26%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9369 93.69%
P-glycoprotein inhibitior - 0.9779 97.79%
P-glycoprotein substrate - 0.9506 95.06%
CYP3A4 substrate - 0.6839 68.39%
CYP2C9 substrate + 0.5942 59.42%
CYP2D6 substrate - 0.8718 87.18%
CYP3A4 inhibition - 0.9669 96.69%
CYP2C9 inhibition - 0.9155 91.55%
CYP2C19 inhibition - 0.9174 91.74%
CYP2D6 inhibition - 0.9530 95.30%
CYP1A2 inhibition - 0.8635 86.35%
CYP2C8 inhibition - 0.9843 98.43%
CYP inhibitory promiscuity - 0.8937 89.37%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6357 63.57%
Carcinogenicity (trinary) Non-required 0.5186 51.86%
Eye corrosion + 0.9875 98.75%
Eye irritation + 0.9889 98.89%
Skin irritation - 0.5881 58.81%
Skin corrosion - 0.9914 99.14%
Ames mutagenesis - 0.9400 94.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7960 79.60%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6407 64.07%
skin sensitisation + 0.8032 80.32%
Respiratory toxicity - 0.9556 95.56%
Reproductive toxicity - 0.9889 98.89%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity + 0.6805 68.05%
Acute Oral Toxicity (c) IV 0.6430 64.30%
Estrogen receptor binding - 0.9553 95.53%
Androgen receptor binding - 0.8293 82.93%
Thyroid receptor binding - 0.8386 83.86%
Glucocorticoid receptor binding - 0.9082 90.82%
Aromatase binding - 0.8307 83.07%
PPAR gamma - 0.9188 91.88%
Honey bee toxicity - 0.9064 90.64%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.6255 62.55%
Fish aquatic toxicity - 0.5104 51.04%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.65% 96.09%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 86.17% 97.21%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.59% 96.95%
CHEMBL2581 P07339 Cathepsin D 82.98% 98.95%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 81.32% 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.
There are no matching plants.

Cross-Links

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PubChem 61914
LOTUS LTS0189048
wikiData Q27268172