8-(6-Methoxy-2-oxochromen-7-yl)oxy-2,6-dimethylocta-2,6-dienal

Details

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Internal ID 19c7cb18-6a6e-4170-815b-36f678a9d17c
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones
IUPAC Name 8-(6-methoxy-2-oxochromen-7-yl)oxy-2,6-dimethylocta-2,6-dienal
SMILES (Canonical) CC(=CCOC1=C(C=C2C=CC(=O)OC2=C1)OC)CCC=C(C)C=O
SMILES (Isomeric) CC(=CCOC1=C(C=C2C=CC(=O)OC2=C1)OC)CCC=C(C)C=O
InChI InChI=1S/C20H22O5/c1-14(5-4-6-15(2)13-21)9-10-24-19-12-17-16(11-18(19)23-3)7-8-20(22)25-17/h6-9,11-13H,4-5,10H2,1-3H3
InChI Key SSKYVKAMMVPTNN-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C20H22O5
Molecular Weight 342.40 g/mol
Exact Mass 342.14672380 g/mol
Topological Polar Surface Area (TPSA) 61.80 Ų
XlogP 3.80
Atomic LogP (AlogP) 4.05
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 8-(6-Methoxy-2-oxochromen-7-yl)oxy-2,6-dimethylocta-2,6-dienal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9756 97.56%
Caco-2 + 0.7628 76.28%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.8063 80.63%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8882 88.82%
OATP1B3 inhibitior + 0.9408 94.08%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9021 90.21%
P-glycoprotein inhibitior + 0.8672 86.72%
P-glycoprotein substrate - 0.5964 59.64%
CYP3A4 substrate + 0.5343 53.43%
CYP2C9 substrate - 0.6120 61.20%
CYP2D6 substrate - 0.8507 85.07%
CYP3A4 inhibition - 0.6395 63.95%
CYP2C9 inhibition - 0.7439 74.39%
CYP2C19 inhibition + 0.8553 85.53%
CYP2D6 inhibition - 0.8705 87.05%
CYP1A2 inhibition + 0.9099 90.99%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity + 0.6194 61.94%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.7406 74.06%
Eye corrosion - 0.9884 98.84%
Eye irritation - 0.8938 89.38%
Skin irritation - 0.8180 81.80%
Skin corrosion - 0.9666 96.66%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8890 88.90%
Micronuclear - 0.7600 76.00%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation - 0.8516 85.16%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.7382 73.82%
Acute Oral Toxicity (c) III 0.4232 42.32%
Estrogen receptor binding + 0.8203 82.03%
Androgen receptor binding + 0.5949 59.49%
Thyroid receptor binding + 0.5327 53.27%
Glucocorticoid receptor binding + 0.8002 80.02%
Aromatase binding + 0.5825 58.25%
PPAR gamma + 0.6170 61.70%
Honey bee toxicity - 0.8909 89.09%
Biodegradation - 0.7000 70.00%
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
CHEMBL3060 Q9Y345 Glycine transporter 2 95.39% 99.17%
CHEMBL3492 P49721 Proteasome Macropain subunit 94.69% 90.24%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.36% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.86% 94.00%
CHEMBL2581 P07339 Cathepsin D 89.50% 98.95%
CHEMBL4208 P20618 Proteasome component C5 89.37% 90.00%
CHEMBL3401 O75469 Pregnane X receptor 89.17% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.78% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.63% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.93% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.03% 96.09%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 84.57% 94.03%
CHEMBL2535 P11166 Glucose transporter 83.72% 98.75%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 82.97% 92.08%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.13% 89.00%

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.
Artemisia keiskeana

Cross-Links

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PubChem 54322219
LOTUS LTS0242852
wikiData Q105259754