6-(7-Hydroperoxy-3,7-dimethylocta-2,5-dienyl)-7-hydroxychromen-2-one

Details

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Internal ID 9b7e1124-67c3-44fc-8c5c-46437e8094b4
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Hydroxycoumarins > 7-hydroxycoumarins
IUPAC Name 6-(7-hydroperoxy-3,7-dimethylocta-2,5-dienyl)-7-hydroxychromen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H22O5/c1-13(5-4-10-19(2,3)24-22)6-7-14-11-15-8-9-18(21)23-17(15)12-16(14)20/h4,6,8-12,20,22H,5,7H2,1-3H3
InChI Key WGLOVOJJZFJYLA-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H22O5
Molecular Weight 330.40 g/mol
Exact Mass 330.14672380 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 3.80
Atomic LogP (AlogP) 4.20
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-(7-Hydroperoxy-3,7-dimethylocta-2,5-dienyl)-7-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 + 0.9846 98.46%
Caco-2 + 0.5995 59.95%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.7105 71.05%
OATP2B1 inhibitior - 0.5786 57.86%
OATP1B1 inhibitior + 0.8523 85.23%
OATP1B3 inhibitior + 0.8212 82.12%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.9168 91.68%
P-glycoprotein inhibitior - 0.6465 64.65%
P-glycoprotein substrate - 0.7559 75.59%
CYP3A4 substrate + 0.5271 52.71%
CYP2C9 substrate - 0.5914 59.14%
CYP2D6 substrate - 0.8276 82.76%
CYP3A4 inhibition - 0.6187 61.87%
CYP2C9 inhibition + 0.6199 61.99%
CYP2C19 inhibition + 0.6221 62.21%
CYP2D6 inhibition - 0.8603 86.03%
CYP1A2 inhibition + 0.6581 65.81%
CYP2C8 inhibition - 0.6261 62.61%
CYP inhibitory promiscuity + 0.6442 64.42%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8513 85.13%
Carcinogenicity (trinary) Non-required 0.6293 62.93%
Eye corrosion - 0.9873 98.73%
Eye irritation - 0.9106 91.06%
Skin irritation - 0.7560 75.60%
Skin corrosion - 0.9416 94.16%
Ames mutagenesis + 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7185 71.85%
Micronuclear - 0.7100 71.00%
Hepatotoxicity - 0.5474 54.74%
skin sensitisation - 0.7564 75.64%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.6769 67.69%
Acute Oral Toxicity (c) III 0.5738 57.38%
Estrogen receptor binding + 0.9512 95.12%
Androgen receptor binding - 0.5626 56.26%
Thyroid receptor binding + 0.7112 71.12%
Glucocorticoid receptor binding + 0.9061 90.61%
Aromatase binding + 0.8362 83.62%
PPAR gamma + 0.8786 87.86%
Honey bee toxicity - 0.8700 87.00%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5400 54.00%
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 99.12% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.37% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 94.40% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.57% 94.00%
CHEMBL3959 P16083 Quinone reductase 2 89.30% 89.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.97% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.28% 86.33%
CHEMBL1937 Q92769 Histone deacetylase 2 88.23% 94.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.41% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.79% 99.17%
CHEMBL1951 P21397 Monoamine oxidase A 85.17% 91.49%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.48% 96.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.27% 96.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.34% 99.23%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 82.13% 80.78%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.04% 89.00%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 81.90% 83.57%

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.
Philotheca tomentella

Cross-Links

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PubChem 163074419
LOTUS LTS0162889
wikiData Q105304615