4',5-Diformyl-2-methoxydiphenylether

Details

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Internal ID a84b1e31-5719-45e9-bb9e-8202519784cb
Taxonomy Benzenoids > Benzene and substituted derivatives > Diphenylethers
IUPAC Name 3-(4-formylphenoxy)-4-methoxybenzaldehyde
SMILES (Canonical) COC1=C(C=C(C=C1)C=O)OC2=CC=C(C=C2)C=O
SMILES (Isomeric) COC1=C(C=C(C=C1)C=O)OC2=CC=C(C=C2)C=O
InChI InChI=1S/C15H12O4/c1-18-14-7-4-12(10-17)8-15(14)19-13-5-2-11(9-16)3-6-13/h2-10H,1H3
InChI Key YAYLLPIGVCCHJD-UHFFFAOYSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C15H12O4
Molecular Weight 256.25 g/mol
Exact Mass 256.07355886 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 1.80
Atomic LogP (AlogP) 3.11
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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4',5-diformyl-2-methoxydiphenylether

2D Structure

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2D Structure of 4',5-Diformyl-2-methoxydiphenylether

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9941 99.41%
Caco-2 + 0.9093 90.93%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.7857 78.57%
Subcellular localzation Mitochondria 0.9074 90.74%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9256 92.56%
OATP1B3 inhibitior + 0.9826 98.26%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.6606 66.06%
P-glycoprotein inhibitior - 0.8137 81.37%
P-glycoprotein substrate - 0.9644 96.44%
CYP3A4 substrate - 0.6036 60.36%
CYP2C9 substrate - 0.8062 80.62%
CYP2D6 substrate - 0.7092 70.92%
CYP3A4 inhibition - 0.7998 79.98%
CYP2C9 inhibition + 0.5082 50.82%
CYP2C19 inhibition + 0.8272 82.72%
CYP2D6 inhibition - 0.9263 92.63%
CYP1A2 inhibition + 0.9531 95.31%
CYP2C8 inhibition - 0.6370 63.70%
CYP inhibitory promiscuity + 0.5658 56.58%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7234 72.34%
Carcinogenicity (trinary) Non-required 0.4875 48.75%
Eye corrosion - 0.8538 85.38%
Eye irritation + 0.9414 94.14%
Skin irritation - 0.6856 68.56%
Skin corrosion - 0.9688 96.88%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6946 69.46%
Micronuclear + 0.5233 52.33%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation - 0.9285 92.85%
Respiratory toxicity - 0.8444 84.44%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.6824 68.24%
Acute Oral Toxicity (c) III 0.6578 65.78%
Estrogen receptor binding + 0.9391 93.91%
Androgen receptor binding - 0.4937 49.37%
Thyroid receptor binding - 0.5398 53.98%
Glucocorticoid receptor binding - 0.5928 59.28%
Aromatase binding + 0.7838 78.38%
PPAR gamma - 0.6813 68.13%
Honey bee toxicity - 0.9014 90.14%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9788 97.88%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.74% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 94.46% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.78% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.44% 96.09%
CHEMBL4208 P20618 Proteasome component C5 90.32% 90.00%
CHEMBL3194 P02766 Transthyretin 86.80% 90.71%
CHEMBL1255126 O15151 Protein Mdm4 85.23% 90.20%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.01% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.00% 91.11%
CHEMBL2535 P11166 Glucose transporter 81.81% 98.75%
CHEMBL3492 P49721 Proteasome Macropain subunit 81.39% 90.24%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 81.30% 96.47%

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.
Gentiana lutea
Ligularia dentata
Sinomenium acutum

Cross-Links

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PubChem 11065027
NPASS NPC183684
LOTUS LTS0180848
wikiData Q105345697