4-(4-Hydroxy-3,7-dimethylocta-2,6-dienoxy)-5-methylchromen-2-one

Details

Top
Internal ID cd84c57e-fc75-44ff-bb0e-d5132ecc1694
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones
IUPAC Name 4-(4-hydroxy-3,7-dimethylocta-2,6-dienoxy)-5-methylchromen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H24O4/c1-13(2)8-9-16(21)14(3)10-11-23-18-12-19(22)24-17-7-5-6-15(4)20(17)18/h5-8,10,12,16,21H,9,11H2,1-4H3
InChI Key XIQXQZGEDPETFJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C20H24O4
Molecular Weight 328.40 g/mol
Exact Mass 328.16745924 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 4.20
Atomic LogP (AlogP) 4.14
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 4-(4-Hydroxy-3,7-dimethylocta-2,6-dienoxy)-5-methylchromen-2-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9881 98.81%
Caco-2 + 0.5663 56.63%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.7668 76.68%
OATP2B1 inhibitior - 0.8594 85.94%
OATP1B1 inhibitior + 0.9293 92.93%
OATP1B3 inhibitior + 0.9282 92.82%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.7353 73.53%
P-glycoprotein inhibitior - 0.5946 59.46%
P-glycoprotein substrate - 0.7688 76.88%
CYP3A4 substrate + 0.5478 54.78%
CYP2C9 substrate - 0.6233 62.33%
CYP2D6 substrate - 0.8025 80.25%
CYP3A4 inhibition - 0.8162 81.62%
CYP2C9 inhibition - 0.6822 68.22%
CYP2C19 inhibition + 0.7616 76.16%
CYP2D6 inhibition - 0.6016 60.16%
CYP1A2 inhibition + 0.8111 81.11%
CYP2C8 inhibition - 0.6179 61.79%
CYP inhibitory promiscuity + 0.5000 50.00%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9413 94.13%
Carcinogenicity (trinary) Non-required 0.7240 72.40%
Eye corrosion - 0.9882 98.82%
Eye irritation - 0.7268 72.68%
Skin irritation - 0.7864 78.64%
Skin corrosion - 0.9708 97.08%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8674 86.74%
Micronuclear - 0.6026 60.26%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation - 0.7616 76.16%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.7190 71.90%
Acute Oral Toxicity (c) III 0.5285 52.85%
Estrogen receptor binding + 0.8355 83.55%
Androgen receptor binding + 0.5560 55.60%
Thyroid receptor binding + 0.5565 55.65%
Glucocorticoid receptor binding + 0.7798 77.98%
Aromatase binding + 0.6636 66.36%
PPAR gamma + 0.7992 79.92%
Honey bee toxicity - 0.8854 88.54%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity + 0.9869 98.69%

Targets

Top

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 97.57% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 97.18% 94.73%
CHEMBL2581 P07339 Cathepsin D 96.48% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.87% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.17% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.32% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.52% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.71% 89.00%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 89.38% 97.21%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.44% 99.17%
CHEMBL1937 Q92769 Histone deacetylase 2 86.20% 94.75%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.00% 96.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.76% 96.00%
CHEMBL240 Q12809 HERG 84.69% 89.76%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 83.47% 93.65%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.91% 85.14%
CHEMBL2535 P11166 Glucose transporter 82.81% 98.75%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.40% 95.50%
CHEMBL4208 P20618 Proteasome component C5 82.36% 90.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.02% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.64% 96.09%

Plants that contains it

Top
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.
Mutisia orbignyana

Cross-Links

Top
PubChem 163057207
LOTUS LTS0187228
wikiData Q105328691