2-Methylidene-3-(5-oxohexyl)butanedioic acid

Details

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Internal ID b520b0f0-8c03-4165-bda2-302992c1e5cf
Taxonomy Organic acids and derivatives > Keto acids and derivatives > Medium-chain keto acids and derivatives
IUPAC Name 2-methylidene-3-(5-oxohexyl)butanedioic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H16O5/c1-7(12)5-3-4-6-9(11(15)16)8(2)10(13)14/h9H,2-6H2,1H3,(H,13,14)(H,15,16)
InChI Key IGSGZWAWTKVRCR-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H16O5
Molecular Weight 228.24 g/mol
Exact Mass 228.09977361 g/mol
Topological Polar Surface Area (TPSA) 91.70 Ų
XlogP 0.80
Atomic LogP (AlogP) 1.48
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Methylidene-3-(5-oxohexyl)butanedioic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8817 88.17%
Caco-2 - 0.6139 61.39%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.7820 78.20%
OATP2B1 inhibitior - 0.8504 85.04%
OATP1B1 inhibitior + 0.9435 94.35%
OATP1B3 inhibitior + 0.9323 93.23%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9756 97.56%
P-glycoprotein inhibitior - 0.9640 96.40%
P-glycoprotein substrate - 0.8775 87.75%
CYP3A4 substrate - 0.6260 62.60%
CYP2C9 substrate + 0.6241 62.41%
CYP2D6 substrate - 0.8944 89.44%
CYP3A4 inhibition - 0.8499 84.99%
CYP2C9 inhibition - 0.8898 88.98%
CYP2C19 inhibition - 0.9165 91.65%
CYP2D6 inhibition - 0.9052 90.52%
CYP1A2 inhibition - 0.6699 66.99%
CYP2C8 inhibition - 0.9781 97.81%
CYP inhibitory promiscuity - 0.9220 92.20%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7158 71.58%
Carcinogenicity (trinary) Non-required 0.6885 68.85%
Eye corrosion - 0.7407 74.07%
Eye irritation + 0.9084 90.84%
Skin irritation - 0.5460 54.60%
Skin corrosion - 0.8764 87.64%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6474 64.74%
Micronuclear - 0.9100 91.00%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation - 0.5910 59.10%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity - 0.8988 89.88%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity + 0.4653 46.53%
Acute Oral Toxicity (c) III 0.6915 69.15%
Estrogen receptor binding - 0.6679 66.79%
Androgen receptor binding - 0.7536 75.36%
Thyroid receptor binding - 0.7833 78.33%
Glucocorticoid receptor binding - 0.5729 57.29%
Aromatase binding - 0.8536 85.36%
PPAR gamma + 0.5686 56.86%
Honey bee toxicity - 0.9569 95.69%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.8600 86.00%
Fish aquatic toxicity + 0.9830 98.30%

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
CHEMBL4040 P28482 MAP kinase ERK2 97.98% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.35% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.54% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.71% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.21% 91.11%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.51% 93.56%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.48% 95.89%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 162816173
LOTUS LTS0032095
wikiData Q104168780