4-Methyl-2-oxopentanoic acid

Details

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Internal ID 607bf209-a8bb-4878-96bd-566f84108170
Taxonomy Organic acids and derivatives > Keto acids and derivatives > Short-chain keto acids and derivatives
IUPAC Name 4-methyl-2-oxopentanoic acid
SMILES (Canonical) CC(C)CC(=O)C(=O)O
SMILES (Isomeric) CC(C)CC(=O)C(=O)O
InChI InChI=1S/C6H10O3/c1-4(2)3-5(7)6(8)9/h4H,3H2,1-2H3,(H,8,9)
InChI Key BKAJNAXTPSGJCU-UHFFFAOYSA-N
Popularity 1,310 references in papers

Physical and Chemical Properties

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Molecular Formula C6H10O3
Molecular Weight 130.14 g/mol
Exact Mass 130.062994177 g/mol
Topological Polar Surface Area (TPSA) 54.40 Ų
XlogP 0.90
Atomic LogP (AlogP) 0.69
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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816-66-0
4-Methyl-2-oxovaleric acid
alpha-Ketoisocaproic acid
Ketoleucine
2-Oxoisocaproate
alpha-ketoisocaproate
2-OXO-4-METHYLPENTANOIC ACID
Pentanoic acid, 4-methyl-2-oxo-
2-Oxoisocaproic acid
4-methyl-2-oxopentanoate
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 4-Methyl-2-oxopentanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9623 96.23%
Caco-2 - 0.6376 63.76%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.8876 88.76%
OATP2B1 inhibitior - 0.8447 84.47%
OATP1B1 inhibitior + 0.9483 94.83%
OATP1B3 inhibitior + 0.9535 95.35%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9487 94.87%
P-glycoprotein inhibitior - 0.9765 97.65%
P-glycoprotein substrate - 0.9764 97.64%
CYP3A4 substrate - 0.7796 77.96%
CYP2C9 substrate + 0.6206 62.06%
CYP2D6 substrate - 0.8857 88.57%
CYP3A4 inhibition - 0.9712 97.12%
CYP2C9 inhibition - 0.9094 90.94%
CYP2C19 inhibition - 0.9616 96.16%
CYP2D6 inhibition - 0.9578 95.78%
CYP1A2 inhibition - 0.9506 95.06%
CYP2C8 inhibition - 0.9973 99.73%
CYP inhibitory promiscuity - 0.9892 98.92%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5292 52.92%
Carcinogenicity (trinary) Non-required 0.7223 72.23%
Eye corrosion + 0.9780 97.80%
Eye irritation + 0.9803 98.03%
Skin irritation + 0.5431 54.31%
Skin corrosion + 0.5848 58.48%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8365 83.65%
Micronuclear - 0.8400 84.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation + 0.6163 61.63%
Respiratory toxicity - 0.8778 87.78%
Reproductive toxicity - 0.8300 83.00%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity + 0.5100 51.00%
Acute Oral Toxicity (c) III 0.5858 58.58%
Estrogen receptor binding - 0.9542 95.42%
Androgen receptor binding - 0.8497 84.97%
Thyroid receptor binding - 0.8915 89.15%
Glucocorticoid receptor binding - 0.9381 93.81%
Aromatase binding - 0.9127 91.27%
PPAR gamma - 0.9465 94.65%
Honey bee toxicity - 0.9861 98.61%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.8800 88.00%
Fish aquatic toxicity - 0.4597 45.97%

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 91.39% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.06% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 85.64% 83.82%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 83.56% 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.
Solanum lycopersicum
Vitis vinifera

Cross-Links

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PubChem 70
NPASS NPC38930
LOTUS LTS0087240
wikiData Q622421