4-Hydroxy-3,5-dimethyl-6-(3-methylpent-1-enyl)oxan-2-one

Details

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Internal ID 923aa6c3-6277-4c4a-9210-b6fd86c3e1e1
Taxonomy Organoheterocyclic compounds > Lactones > Delta valerolactones
IUPAC Name 4-hydroxy-3,5-dimethyl-6-(3-methylpent-1-enyl)oxan-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H22O3/c1-5-8(2)6-7-11-9(3)12(14)10(4)13(15)16-11/h6-12,14H,5H2,1-4H3
InChI Key ILDJSXPOMKNCOL-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C13H22O3
Molecular Weight 226.31 g/mol
Exact Mass 226.15689456 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.15
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-Hydroxy-3,5-dimethyl-6-(3-methylpent-1-enyl)oxan-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 + 0.9801 98.01%
Caco-2 + 0.6435 64.35%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.5749 57.49%
OATP2B1 inhibitior - 0.8590 85.90%
OATP1B1 inhibitior + 0.8740 87.40%
OATP1B3 inhibitior + 0.9715 97.15%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8050 80.50%
P-glycoprotein inhibitior - 0.9057 90.57%
P-glycoprotein substrate - 0.8977 89.77%
CYP3A4 substrate - 0.5423 54.23%
CYP2C9 substrate - 0.8537 85.37%
CYP2D6 substrate - 0.8640 86.40%
CYP3A4 inhibition - 0.8858 88.58%
CYP2C9 inhibition - 0.9252 92.52%
CYP2C19 inhibition - 0.8646 86.46%
CYP2D6 inhibition - 0.9563 95.63%
CYP1A2 inhibition - 0.9127 91.27%
CYP2C8 inhibition - 0.9769 97.69%
CYP inhibitory promiscuity - 0.8995 89.95%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8328 83.28%
Carcinogenicity (trinary) Non-required 0.5853 58.53%
Eye corrosion - 0.8371 83.71%
Eye irritation - 0.9896 98.96%
Skin irritation + 0.6275 62.75%
Skin corrosion - 0.8468 84.68%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6568 65.68%
Micronuclear - 0.5800 58.00%
Hepatotoxicity + 0.5087 50.87%
skin sensitisation - 0.5580 55.80%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity - 0.7222 72.22%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity - 0.6610 66.10%
Acute Oral Toxicity (c) III 0.6363 63.63%
Estrogen receptor binding - 0.7770 77.70%
Androgen receptor binding - 0.7803 78.03%
Thyroid receptor binding - 0.6781 67.81%
Glucocorticoid receptor binding - 0.7325 73.25%
Aromatase binding - 0.7981 79.81%
PPAR gamma - 0.7019 70.19%
Honey bee toxicity - 0.7679 76.79%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity + 0.8189 81.89%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.44% 97.25%
CHEMBL2581 P07339 Cathepsin D 93.26% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 88.59% 91.49%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.22% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.76% 91.11%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 86.13% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.00% 95.56%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 84.90% 89.34%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.81% 85.14%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 84.17% 94.80%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.72% 89.00%

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 76418366
LOTUS LTS0102168
wikiData Q104168893