7-(3,7-Dimethylocta-2,6-dienoxy)-5-hydroxychromen-2-one

Details

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Internal ID 74d2bae1-8989-4478-86dc-74be00e7b401
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones
IUPAC Name 7-(3,7-dimethylocta-2,6-dienoxy)-5-hydroxychromen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H22O4/c1-13(2)5-4-6-14(3)9-10-22-15-11-17(20)16-7-8-19(21)23-18(16)12-15/h5,7-9,11-12,20H,4,6,10H2,1-3H3
InChI Key IMUPQGLYMLQRFJ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H22O4
Molecular Weight 314.40 g/mol
Exact Mass 314.15180918 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 4.90
Atomic LogP (AlogP) 4.57
H-Bond Acceptor 4
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 7-(3,7-Dimethylocta-2,6-dienoxy)-5-hydroxychromen-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 + 0.9853 98.53%
Caco-2 + 0.7725 77.25%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.6853 68.53%
OATP2B1 inhibitior - 0.7157 71.57%
OATP1B1 inhibitior + 0.9062 90.62%
OATP1B3 inhibitior + 0.8697 86.97%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.7305 73.05%
P-glycoprotein inhibitior - 0.5000 50.00%
P-glycoprotein substrate - 0.8482 84.82%
CYP3A4 substrate + 0.5464 54.64%
CYP2C9 substrate - 0.6172 61.72%
CYP2D6 substrate - 0.8048 80.48%
CYP3A4 inhibition + 0.5515 55.15%
CYP2C9 inhibition + 0.7215 72.15%
CYP2C19 inhibition + 0.8784 87.84%
CYP2D6 inhibition - 0.5194 51.94%
CYP1A2 inhibition + 0.9218 92.18%
CYP2C8 inhibition - 0.5848 58.48%
CYP inhibitory promiscuity + 0.5221 52.21%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.7265 72.65%
Eye corrosion - 0.9891 98.91%
Eye irritation - 0.7291 72.91%
Skin irritation - 0.8051 80.51%
Skin corrosion - 0.9698 96.98%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3717 37.17%
Micronuclear - 0.7900 79.00%
Hepatotoxicity + 0.5667 56.67%
skin sensitisation - 0.7902 79.02%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.6288 62.88%
Acute Oral Toxicity (c) III 0.5986 59.86%
Estrogen receptor binding + 0.8550 85.50%
Androgen receptor binding + 0.8396 83.96%
Thyroid receptor binding + 0.5750 57.50%
Glucocorticoid receptor binding + 0.7373 73.73%
Aromatase binding + 0.7853 78.53%
PPAR gamma + 0.8826 88.26%
Honey bee toxicity - 0.8451 84.51%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5500 55.00%
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 99.17% 91.11%
CHEMBL2039 P27338 Monoamine oxidase B 96.31% 92.51%
CHEMBL2581 P07339 Cathepsin D 95.50% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.42% 94.45%
CHEMBL1951 P21397 Monoamine oxidase A 95.11% 91.49%
CHEMBL3401 O75469 Pregnane X receptor 94.99% 94.73%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 94.90% 92.08%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.39% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.80% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.96% 89.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.99% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.77% 94.00%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 86.66% 83.57%
CHEMBL4208 P20618 Proteasome component C5 84.94% 90.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.69% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.91% 86.33%

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.
Clausena excavata

Cross-Links

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PubChem 162851811
LOTUS LTS0183452
wikiData Q105115935