methyl (2E,3E,5E)-2-(methoxymethylidene)-6-(4-methoxyphenyl)-3-methylhexa-3,5-dienoate

Details

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Internal ID cb49ca1f-b948-44f8-af3c-67cba6e8d810
Taxonomy Benzenoids > Phenol ethers > Anisoles
IUPAC Name methyl (2E,3E,5E)-2-(methoxymethylidene)-6-(4-methoxyphenyl)-3-methylhexa-3,5-dienoate
SMILES (Canonical) CC(=CC=CC1=CC=C(C=C1)OC)C(=COC)C(=O)OC
SMILES (Isomeric) C/C(=C\C=C\C1=CC=C(C=C1)OC)/C(=C\OC)/C(=O)OC
InChI InChI=1S/C17H20O4/c1-13(16(12-19-2)17(18)21-4)6-5-7-14-8-10-15(20-3)11-9-14/h5-12H,1-4H3/b7-5+,13-6+,16-12+
InChI Key VHMKGBYCXDBNFU-ZXCICTMFSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H20O4
Molecular Weight 288.34 g/mol
Exact Mass 288.13615911 g/mol
Topological Polar Surface Area (TPSA) 44.80 Ų
XlogP 3.80
Atomic LogP (AlogP) 3.36
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of methyl (2E,3E,5E)-2-(methoxymethylidene)-6-(4-methoxyphenyl)-3-methylhexa-3,5-dienoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9954 99.54%
Caco-2 + 0.9514 95.14%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.8212 82.12%
OATP2B1 inhibitior - 0.8596 85.96%
OATP1B1 inhibitior + 0.9316 93.16%
OATP1B3 inhibitior + 0.9667 96.67%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.7345 73.45%
P-glycoprotein inhibitior + 0.6457 64.57%
P-glycoprotein substrate - 0.8742 87.42%
CYP3A4 substrate + 0.5084 50.84%
CYP2C9 substrate - 0.6133 61.33%
CYP2D6 substrate - 0.8278 82.78%
CYP3A4 inhibition - 0.6480 64.80%
CYP2C9 inhibition - 0.9648 96.48%
CYP2C19 inhibition - 0.6050 60.50%
CYP2D6 inhibition - 0.9627 96.27%
CYP1A2 inhibition - 0.6308 63.08%
CYP2C8 inhibition - 0.7435 74.35%
CYP inhibitory promiscuity + 0.5344 53.44%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5660 56.60%
Carcinogenicity (trinary) Non-required 0.6058 60.58%
Eye corrosion - 0.8456 84.56%
Eye irritation - 0.5712 57.12%
Skin irritation - 0.6984 69.84%
Skin corrosion - 0.9952 99.52%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7234 72.34%
Micronuclear + 0.5400 54.00%
Hepatotoxicity - 0.5717 57.17%
skin sensitisation - 0.7679 76.79%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity + 0.6701 67.01%
Acute Oral Toxicity (c) III 0.4405 44.05%
Estrogen receptor binding + 0.8870 88.70%
Androgen receptor binding + 0.6764 67.64%
Thyroid receptor binding + 0.6943 69.43%
Glucocorticoid receptor binding - 0.6483 64.83%
Aromatase binding + 0.7224 72.24%
PPAR gamma - 0.5352 53.52%
Honey bee toxicity - 0.8789 87.89%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9693 96.93%

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 96.14% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 94.98% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.00% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.51% 95.56%
CHEMBL4208 P20618 Proteasome component C5 91.01% 90.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.60% 99.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 86.38% 95.50%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.72% 86.33%
CHEMBL3492 P49721 Proteasome Macropain subunit 82.50% 90.24%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 6510108
LOTUS LTS0265408
wikiData Q105286495