2-(5-Ethenyl-2,5-dimethyloxolan-2-yl)-6-hydroxy-6-methylhept-4-en-3-one

Details

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Internal ID 6919d300-7750-4df7-99a8-de4a28612976
Taxonomy Organoheterocyclic compounds > Tetrahydrofurans
IUPAC Name 2-(5-ethenyl-2,5-dimethyloxolan-2-yl)-6-hydroxy-6-methylhept-4-en-3-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H26O3/c1-7-15(5)10-11-16(6,19-15)12(2)13(17)8-9-14(3,4)18/h7-9,12,18H,1,10-11H2,2-6H3
InChI Key IYHIOPKYJASMTA-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H26O3
Molecular Weight 266.38 g/mol
Exact Mass 266.18819469 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 2.10
Atomic LogP (AlogP) 3.03
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 2-(5-Ethenyl-2,5-dimethyloxolan-2-yl)-6-hydroxy-6-methylhept-4-en-3-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9837 98.37%
Caco-2 + 0.5849 58.49%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.5347 53.47%
OATP2B1 inhibitior - 0.8563 85.63%
OATP1B1 inhibitior + 0.9097 90.97%
OATP1B3 inhibitior + 0.9300 93.00%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.8939 89.39%
P-glycoprotein inhibitior - 0.8841 88.41%
P-glycoprotein substrate - 0.8688 86.88%
CYP3A4 substrate + 0.5595 55.95%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8688 86.88%
CYP3A4 inhibition - 0.7713 77.13%
CYP2C9 inhibition - 0.7773 77.73%
CYP2C19 inhibition - 0.7811 78.11%
CYP2D6 inhibition - 0.9425 94.25%
CYP1A2 inhibition - 0.6461 64.61%
CYP2C8 inhibition - 0.9237 92.37%
CYP inhibitory promiscuity - 0.9161 91.61%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7728 77.28%
Carcinogenicity (trinary) Non-required 0.5534 55.34%
Eye corrosion - 0.7872 78.72%
Eye irritation - 0.8625 86.25%
Skin irritation + 0.6415 64.15%
Skin corrosion - 0.7944 79.44%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5715 57.15%
Micronuclear - 0.9000 90.00%
Hepatotoxicity + 0.6177 61.77%
skin sensitisation + 0.6844 68.44%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity - 0.6889 68.89%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity + 0.6067 60.67%
Acute Oral Toxicity (c) III 0.6860 68.60%
Estrogen receptor binding + 0.5838 58.38%
Androgen receptor binding - 0.7100 71.00%
Thyroid receptor binding + 0.5786 57.86%
Glucocorticoid receptor binding - 0.5000 50.00%
Aromatase binding - 0.5083 50.83%
PPAR gamma - 0.5847 58.47%
Honey bee toxicity - 0.7973 79.73%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.7900 79.00%
Fish aquatic toxicity + 0.7117 71.17%

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 92.59% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.03% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.73% 96.09%
CHEMBL3359 P21462 Formyl peptide receptor 1 85.25% 93.56%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 83.98% 92.88%
CHEMBL2581 P07339 Cathepsin D 83.39% 98.95%
CHEMBL1293316 Q9HBX9 Relaxin receptor 1 81.94% 82.50%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.83% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.28% 89.00%
CHEMBL4246 P42680 Tyrosine-protein kinase TEC 80.68% 82.05%
CHEMBL268 P43235 Cathepsin K 80.67% 96.85%

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.
Artemisia abrotanum

Cross-Links

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PubChem 85126593
LOTUS LTS0177455
wikiData Q105122753