4-Methyl-2-propan-2-ylpentanoate

Details

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Internal ID d1ceafc1-9e39-4bde-8f71-1352af8a974f
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Branched fatty acids > Methyl-branched fatty acids
IUPAC Name 4-methyl-2-propan-2-ylpentanoate
SMILES (Canonical) CC(C)CC(C(C)C)C(=O)[O-]
SMILES (Isomeric) CC(C)CC(C(C)C)C(=O)[O-]
InChI InChI=1S/C9H18O2/c1-6(2)5-8(7(3)4)9(10)11/h6-8H,5H2,1-4H3,(H,10,11)/p-1
InChI Key FVTYKVHAFJRVJE-UHFFFAOYSA-M
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C9H17O2-
Molecular Weight 157.23 g/mol
Exact Mass 157.122854781 g/mol
Topological Polar Surface Area (TPSA) 40.10 Ų
XlogP 3.40
Atomic LogP (AlogP) 1.05
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-Methyl-2-propan-2-ylpentanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9813 98.13%
Caco-2 - 0.6423 64.23%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.6239 62.39%
OATP2B1 inhibitior - 0.8342 83.42%
OATP1B1 inhibitior + 0.9465 94.65%
OATP1B3 inhibitior + 0.9373 93.73%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9673 96.73%
P-glycoprotein inhibitior - 0.9643 96.43%
P-glycoprotein substrate - 0.9126 91.26%
CYP3A4 substrate - 0.7068 70.68%
CYP2C9 substrate + 0.6453 64.53%
CYP2D6 substrate - 0.8931 89.31%
CYP3A4 inhibition - 0.9883 98.83%
CYP2C9 inhibition - 0.9373 93.73%
CYP2C19 inhibition - 0.9657 96.57%
CYP2D6 inhibition - 0.9453 94.53%
CYP1A2 inhibition - 0.8855 88.55%
CYP2C8 inhibition - 0.9932 99.32%
CYP inhibitory promiscuity - 0.9720 97.20%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6357 63.57%
Carcinogenicity (trinary) Non-required 0.7025 70.25%
Eye corrosion + 0.9925 99.25%
Eye irritation + 0.9317 93.17%
Skin irritation + 0.8101 81.01%
Skin corrosion - 0.5979 59.79%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7448 74.48%
Micronuclear - 0.9100 91.00%
Hepatotoxicity + 0.8125 81.25%
skin sensitisation - 0.7291 72.91%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.7570 75.70%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity + 0.6243 62.43%
Acute Oral Toxicity (c) III 0.5745 57.45%
Estrogen receptor binding - 0.8936 89.36%
Androgen receptor binding - 0.7557 75.57%
Thyroid receptor binding - 0.8822 88.22%
Glucocorticoid receptor binding - 0.9258 92.58%
Aromatase binding - 0.8863 88.63%
PPAR gamma - 0.9122 91.22%
Honey bee toxicity - 0.9495 94.95%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.8800 88.00%
Fish aquatic toxicity + 0.8736 87.36%

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
CHEMBL2581 P07339 Cathepsin D 95.16% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.90% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 90.66% 83.82%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.43% 97.25%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.59% 93.56%
CHEMBL268 P43235 Cathepsin K 84.03% 96.85%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 83.69% 100.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.29% 90.71%

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.
Elsholtzia ciliata
Piper longum

Cross-Links

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PubChem 23617109
NPASS NPC307858