MF-EA-705beta

Details

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Internal ID 81a7c1b4-5214-4fd9-9f76-6fcd350e9037
Taxonomy Benzenoids > Benzene and substituted derivatives > Phenylpropenes
IUPAC Name (3E,5E,7Z)-8-[2-[(Z)-but-1-enyl]-4-methylphenyl]nona-3,5,7-trienoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H24O2/c1-4-5-11-18-15-16(2)13-14-19(18)17(3)10-8-6-7-9-12-20(21)22/h5-11,13-15H,4,12H2,1-3H3,(H,21,22)/b8-6+,9-7+,11-5-,17-10-
InChI Key NEWBSSHUUPIRNQ-BDPLXOTQSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H24O2
Molecular Weight 296.40 g/mol
Exact Mass 296.177630004 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 5.70
Atomic LogP (AlogP) 5.41
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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(3E,5E,7Z)-8-[2-[(Z)-but-1-enyl]-4-methylphenyl]nona-3,5,7-trienoic acid

2D Structure

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2D Structure of MF-EA-705beta

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.7792 77.92%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.7023 70.23%
OATP2B1 inhibitior - 0.7145 71.45%
OATP1B1 inhibitior + 0.8468 84.68%
OATP1B3 inhibitior + 0.9554 95.54%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.9818 98.18%
P-glycoprotein inhibitior - 0.6806 68.06%
P-glycoprotein substrate - 0.8907 89.07%
CYP3A4 substrate - 0.5949 59.49%
CYP2C9 substrate - 0.7928 79.28%
CYP2D6 substrate - 0.8627 86.27%
CYP3A4 inhibition - 0.9112 91.12%
CYP2C9 inhibition - 0.8982 89.82%
CYP2C19 inhibition - 0.8845 88.45%
CYP2D6 inhibition - 0.8873 88.73%
CYP1A2 inhibition - 0.8929 89.29%
CYP2C8 inhibition - 0.6804 68.04%
CYP inhibitory promiscuity - 0.7114 71.14%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5040 50.40%
Carcinogenicity (trinary) Non-required 0.7251 72.51%
Eye corrosion - 0.9429 94.29%
Eye irritation - 0.8686 86.86%
Skin irritation + 0.7136 71.36%
Skin corrosion - 0.8974 89.74%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7723 77.23%
Micronuclear - 0.8393 83.93%
Hepatotoxicity + 0.5927 59.27%
skin sensitisation + 0.9119 91.19%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity - 0.6095 60.95%
Acute Oral Toxicity (c) III 0.8889 88.89%
Estrogen receptor binding + 0.9360 93.60%
Androgen receptor binding + 0.5583 55.83%
Thyroid receptor binding + 0.7509 75.09%
Glucocorticoid receptor binding + 0.7963 79.63%
Aromatase binding + 0.9165 91.65%
PPAR gamma + 0.7668 76.68%
Honey bee toxicity - 0.9658 96.58%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 0.9669 96.69%

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
CHEMBL2581 P07339 Cathepsin D 95.20% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.19% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 89.72% 94.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.07% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.85% 95.56%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 87.38% 91.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.08% 86.33%
CHEMBL221 P23219 Cyclooxygenase-1 84.53% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.73% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.48% 99.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.65% 95.50%

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 11781445
LOTUS LTS0130175
wikiData Q75069711