8-(3,7-Dimethylocta-2,6-dienoxy)-7-hydroxychromen-2-one

Details

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Internal ID a44ec55f-5c9b-4650-9fb2-73f2fb9aff98
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones
IUPAC Name 8-(3,7-dimethylocta-2,6-dienoxy)-7-hydroxychromen-2-one
SMILES (Canonical) CC(=CCCC(=CCOC1=C(C=CC2=C1OC(=O)C=C2)O)C)C
SMILES (Isomeric) CC(=CCCC(=CCOC1=C(C=CC2=C1OC(=O)C=C2)O)C)C
InChI InChI=1S/C19H22O4/c1-13(2)5-4-6-14(3)11-12-22-19-16(20)9-7-15-8-10-17(21)23-18(15)19/h5,7-11,20H,4,6,12H2,1-3H3
InChI Key DHSIDRKPBYDKHG-UHFFFAOYSA-N
Popularity 0 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 8-(3,7-Dimethylocta-2,6-dienoxy)-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 + 0.9601 96.01%
Caco-2 + 0.6913 69.13%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.8280 82.80%
OATP2B1 inhibitior - 0.8593 85.93%
OATP1B1 inhibitior + 0.9262 92.62%
OATP1B3 inhibitior + 0.8784 87.84%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.8631 86.31%
P-glycoprotein inhibitior - 0.4456 44.56%
P-glycoprotein substrate - 0.9197 91.97%
CYP3A4 substrate - 0.5184 51.84%
CYP2C9 substrate - 0.6172 61.72%
CYP2D6 substrate - 0.8048 80.48%
CYP3A4 inhibition - 0.7193 71.93%
CYP2C9 inhibition + 0.6962 69.62%
CYP2C19 inhibition + 0.8896 88.96%
CYP2D6 inhibition - 0.6520 65.20%
CYP1A2 inhibition + 0.9548 95.48%
CYP2C8 inhibition - 0.7185 71.85%
CYP inhibitory promiscuity + 0.5828 58.28%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.7442 74.42%
Eye corrosion - 0.9919 99.19%
Eye irritation + 0.5798 57.98%
Skin irritation - 0.7710 77.10%
Skin corrosion - 0.9623 96.23%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3771 37.71%
Micronuclear - 0.8000 80.00%
Hepatotoxicity + 0.8000 80.00%
skin sensitisation - 0.8121 81.21%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity + 0.5184 51.84%
Acute Oral Toxicity (c) III 0.5343 53.43%
Estrogen receptor binding + 0.7912 79.12%
Androgen receptor binding + 0.7342 73.42%
Thyroid receptor binding + 0.6860 68.60%
Glucocorticoid receptor binding + 0.8142 81.42%
Aromatase binding + 0.6500 65.00%
PPAR gamma + 0.8423 84.23%
Honey bee toxicity - 0.8896 88.96%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5900 59.00%
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 96.31% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 94.43% 94.73%
CHEMBL2581 P07339 Cathepsin D 92.48% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.38% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.20% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.05% 99.23%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 85.59% 92.08%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.52% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.14% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.10% 99.15%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 83.13% 85.30%
CHEMBL4208 P20618 Proteasome component C5 82.82% 90.00%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 82.29% 93.10%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 81.72% 83.57%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.67% 86.33%
CHEMBL1937 Q92769 Histone deacetylase 2 80.21% 94.75%

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.
Feroniella lucida

Cross-Links

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PubChem 163029749
LOTUS LTS0213508
wikiData Q104980808