4-Methyl-5-(7-oxooct-2-enyl)oxolan-2-one

Details

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Internal ID d94534c3-4b30-430c-adff-e80ae70f47f2
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name 4-methyl-5-(7-oxooct-2-enyl)oxolan-2-one
SMILES (Canonical) CC1CC(=O)OC1CC=CCCCC(=O)C
SMILES (Isomeric) CC1CC(=O)OC1CC=CCCCC(=O)C
InChI InChI=1S/C13H20O3/c1-10-9-13(15)16-12(10)8-6-4-3-5-7-11(2)14/h4,6,10,12H,3,5,7-9H2,1-2H3
InChI Key HOMZLLIQOYSYNB-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H20O3
Molecular Weight 224.30 g/mol
Exact Mass 224.14124450 g/mol
Topological Polar Surface Area (TPSA) 43.40 Ų
XlogP 1.90
Atomic LogP (AlogP) 2.64
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-Methyl-5-(7-oxooct-2-enyl)oxolan-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9905 99.05%
Caco-2 - 0.5457 54.57%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.7252 72.52%
OATP2B1 inhibitior - 0.8521 85.21%
OATP1B1 inhibitior + 0.8160 81.60%
OATP1B3 inhibitior + 0.9368 93.68%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior - 0.6618 66.18%
P-glycoprotein inhibitior - 0.9432 94.32%
P-glycoprotein substrate - 0.8744 87.44%
CYP3A4 substrate - 0.5104 51.04%
CYP2C9 substrate - 0.8242 82.42%
CYP2D6 substrate - 0.8691 86.91%
CYP3A4 inhibition - 0.8724 87.24%
CYP2C9 inhibition - 0.9428 94.28%
CYP2C19 inhibition - 0.8744 87.44%
CYP2D6 inhibition - 0.9372 93.72%
CYP1A2 inhibition - 0.7500 75.00%
CYP2C8 inhibition - 0.9210 92.10%
CYP inhibitory promiscuity - 0.9233 92.33%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9428 94.28%
Carcinogenicity (trinary) Non-required 0.7178 71.78%
Eye corrosion - 0.8699 86.99%
Eye irritation + 0.5301 53.01%
Skin irritation + 0.6459 64.59%
Skin corrosion - 0.8914 89.14%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4290 42.90%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.7078 70.78%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.8556 85.56%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity - 0.6368 63.68%
Acute Oral Toxicity (c) III 0.7923 79.23%
Estrogen receptor binding - 0.8452 84.52%
Androgen receptor binding - 0.8650 86.50%
Thyroid receptor binding - 0.7895 78.95%
Glucocorticoid receptor binding - 0.5084 50.84%
Aromatase binding - 0.7592 75.92%
PPAR gamma - 0.5000 50.00%
Honey bee toxicity - 0.9384 93.84%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 0.9788 97.88%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.51% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.71% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.66% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.20% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.87% 97.25%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 85.08% 89.34%
CHEMBL3401 O75469 Pregnane X receptor 80.21% 94.73%

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 162914681
LOTUS LTS0137004
wikiData Q104168057