7-(3,7-Dimethyl-5-oxoocta-2,6-dienoxy)chromen-2-one

Details

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Internal ID 4867474e-8753-45e3-a9d9-f9f79f2ab640
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones
IUPAC Name 7-(3,7-dimethyl-5-oxoocta-2,6-dienoxy)chromen-2-one
SMILES (Canonical) CC(=CC(=O)CC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)C
SMILES (Isomeric) CC(=CC(=O)CC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)C
InChI InChI=1S/C19H20O4/c1-13(2)10-16(20)11-14(3)8-9-22-17-6-4-15-5-7-19(21)23-18(15)12-17/h4-8,10,12H,9,11H2,1-3H3
InChI Key JONVYPGHELSEDP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H20O4
Molecular Weight 312.40 g/mol
Exact Mass 312.13615911 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 4.10
Atomic LogP (AlogP) 4.04
H-Bond Acceptor 4
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 7-(3,7-Dimethyl-5-oxoocta-2,6-dienoxy)chromen-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 + 0.9916 99.16%
Caco-2 + 0.7539 75.39%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.7611 76.11%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8669 86.69%
OATP1B3 inhibitior + 0.8790 87.90%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.8307 83.07%
P-glycoprotein inhibitior - 0.5497 54.97%
P-glycoprotein substrate - 0.7883 78.83%
CYP3A4 substrate + 0.5198 51.98%
CYP2C9 substrate - 0.7817 78.17%
CYP2D6 substrate - 0.8635 86.35%
CYP3A4 inhibition + 0.5128 51.28%
CYP2C9 inhibition + 0.6977 69.77%
CYP2C19 inhibition + 0.8365 83.65%
CYP2D6 inhibition - 0.7809 78.09%
CYP1A2 inhibition + 0.8309 83.09%
CYP2C8 inhibition - 0.7183 71.83%
CYP inhibitory promiscuity + 0.6617 66.17%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9513 95.13%
Carcinogenicity (trinary) Non-required 0.6322 63.22%
Eye corrosion - 0.9834 98.34%
Eye irritation - 0.8852 88.52%
Skin irritation - 0.8165 81.65%
Skin corrosion - 0.9718 97.18%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8391 83.91%
Micronuclear - 0.6600 66.00%
Hepatotoxicity + 0.5042 50.42%
skin sensitisation - 0.7304 73.04%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.6151 61.51%
Acute Oral Toxicity (c) III 0.6244 62.44%
Estrogen receptor binding + 0.8778 87.78%
Androgen receptor binding + 0.8450 84.50%
Thyroid receptor binding - 0.6099 60.99%
Glucocorticoid receptor binding + 0.7522 75.22%
Aromatase binding + 0.7032 70.32%
PPAR gamma + 0.6211 62.11%
Honey bee toxicity - 0.8994 89.94%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 1.0000 100.00%

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 97.76% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.89% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 94.46% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.78% 94.00%
CHEMBL4208 P20618 Proteasome component C5 92.39% 90.00%
CHEMBL2581 P07339 Cathepsin D 91.05% 98.95%
CHEMBL2039 P27338 Monoamine oxidase B 89.46% 92.51%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 87.54% 81.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.27% 94.45%
CHEMBL1951 P21397 Monoamine oxidase A 85.09% 91.49%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.02% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.19% 96.09%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 83.52% 89.34%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.03% 90.71%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.65% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.62% 86.33%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 81.99% 87.67%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.88% 95.56%

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.
Baccharis darwinii

Cross-Links

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PubChem 72730526
LOTUS LTS0037301
wikiData Q105132442