4-Methyl-5-oxo-2-pentyloxolane-3-carboxylic acid

Details

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Internal ID 358819bc-6a9b-4fef-a6bf-3c91b919754f
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name 4-methyl-5-oxo-2-pentyloxolane-3-carboxylic acid
SMILES (Canonical) CCCCCC1C(C(C(=O)O1)C)C(=O)O
SMILES (Isomeric) CCCCCC1C(C(C(=O)O1)C)C(=O)O
InChI InChI=1S/C11H18O4/c1-3-4-5-6-8-9(10(12)13)7(2)11(14)15-8/h7-9H,3-6H2,1-2H3,(H,12,13)
InChI Key VRNXAQRALVPTGJ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C11H18O4
Molecular Weight 214.26 g/mol
Exact Mass 214.12050905 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 2.30
Atomic LogP (AlogP) 1.83
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-Methyl-5-oxo-2-pentyloxolane-3-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9221 92.21%
Caco-2 + 0.6013 60.13%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7415 74.15%
OATP2B1 inhibitior - 0.8479 84.79%
OATP1B1 inhibitior + 0.8715 87.15%
OATP1B3 inhibitior + 0.9431 94.31%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.9751 97.51%
P-glycoprotein inhibitior - 0.9172 91.72%
P-glycoprotein substrate - 0.8645 86.45%
CYP3A4 substrate - 0.6166 61.66%
CYP2C9 substrate + 0.6248 62.48%
CYP2D6 substrate - 0.8868 88.68%
CYP3A4 inhibition - 0.7122 71.22%
CYP2C9 inhibition - 0.8468 84.68%
CYP2C19 inhibition - 0.8241 82.41%
CYP2D6 inhibition - 0.9184 91.84%
CYP1A2 inhibition - 0.8313 83.13%
CYP2C8 inhibition - 0.9551 95.51%
CYP inhibitory promiscuity - 0.9426 94.26%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.7134 71.34%
Eye corrosion - 0.9416 94.16%
Eye irritation - 0.7538 75.38%
Skin irritation + 0.5643 56.43%
Skin corrosion - 0.6928 69.28%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7700 77.00%
Micronuclear - 0.9400 94.00%
Hepatotoxicity + 0.6459 64.59%
skin sensitisation - 0.8996 89.96%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity - 0.7000 70.00%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity + 0.6364 63.64%
Acute Oral Toxicity (c) III 0.6021 60.21%
Estrogen receptor binding + 0.5778 57.78%
Androgen receptor binding - 0.5400 54.00%
Thyroid receptor binding - 0.7435 74.35%
Glucocorticoid receptor binding - 0.5211 52.11%
Aromatase binding - 0.8858 88.58%
PPAR gamma - 0.6167 61.67%
Honey bee toxicity - 0.9885 98.85%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.5888 58.88%
Fish aquatic toxicity + 0.9249 92.49%

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 94.11% 83.82%
CHEMBL2581 P07339 Cathepsin D 93.53% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.50% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.36% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.00% 99.17%
CHEMBL230 P35354 Cyclooxygenase-2 87.76% 89.63%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.23% 95.56%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 80.09% 96.00%

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 13888653
LOTUS LTS0056629
wikiData Q77517162