6-Hydroxy-2,6-dimethyl-1-(4-methylfuran-2-yl)octa-2,7-dien-1-one

Details

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Internal ID 4c61b563-cb14-47f0-92b1-585b44ccb150
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Aromatic monoterpenoids
IUPAC Name 6-hydroxy-2,6-dimethyl-1-(4-methylfuran-2-yl)octa-2,7-dien-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H20O3/c1-5-15(4,17)8-6-7-12(3)14(16)13-9-11(2)10-18-13/h5,7,9-10,17H,1,6,8H2,2-4H3
InChI Key MMJJWZIDBAJCJK-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H20O3
Molecular Weight 248.32 g/mol
Exact Mass 248.14124450 g/mol
Topological Polar Surface Area (TPSA) 50.40 Ų
XlogP 3.00
Atomic LogP (AlogP) 3.43
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-Hydroxy-2,6-dimethyl-1-(4-methylfuran-2-yl)octa-2,7-dien-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9921 99.21%
Caco-2 + 0.5409 54.09%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.5248 52.48%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8773 87.73%
OATP1B3 inhibitior + 0.9305 93.05%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.5852 58.52%
P-glycoprotein inhibitior - 0.9180 91.80%
P-glycoprotein substrate - 0.9070 90.70%
CYP3A4 substrate + 0.5117 51.17%
CYP2C9 substrate - 0.8024 80.24%
CYP2D6 substrate - 0.8418 84.18%
CYP3A4 inhibition - 0.5117 51.17%
CYP2C9 inhibition - 0.7186 71.86%
CYP2C19 inhibition - 0.6955 69.55%
CYP2D6 inhibition - 0.8938 89.38%
CYP1A2 inhibition - 0.5946 59.46%
CYP2C8 inhibition - 0.6890 68.90%
CYP inhibitory promiscuity - 0.7553 75.53%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.7928 79.28%
Carcinogenicity (trinary) Non-required 0.5584 55.84%
Eye corrosion - 0.9514 95.14%
Eye irritation - 0.5595 55.95%
Skin irritation + 0.5369 53.69%
Skin corrosion - 0.8434 84.34%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4230 42.30%
Micronuclear - 0.8700 87.00%
Hepatotoxicity - 0.5173 51.73%
skin sensitisation + 0.6718 67.18%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.6531 65.31%
Acute Oral Toxicity (c) III 0.6280 62.80%
Estrogen receptor binding - 0.5675 56.75%
Androgen receptor binding - 0.4873 48.73%
Thyroid receptor binding - 0.5369 53.69%
Glucocorticoid receptor binding + 0.6607 66.07%
Aromatase binding - 0.5000 50.00%
PPAR gamma + 0.8324 83.24%
Honey bee toxicity - 0.8318 83.18%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.8472 84.72%

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
CHEMBL3401 O75469 Pregnane X receptor 96.23% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.95% 91.11%
CHEMBL2581 P07339 Cathepsin D 91.75% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.06% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.04% 86.33%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 86.49% 90.93%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 86.43% 93.65%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.69% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.74% 95.56%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.14% 89.34%

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.
Vernonanthura polyanthes

Cross-Links

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PubChem 163049803
LOTUS LTS0124935
wikiData Q105167798