Perrottetin E 11'-Methyl Ether

Details

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Internal ID 6c0919f1-1532-4ba0-914b-47236252ef80
Taxonomy Lignans, neolignans and related compounds
IUPAC Name 2-[4-[2-(3-hydroxyphenyl)ethyl]phenoxy]-4-[2-(3-methoxyphenyl)ethyl]phenol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C29H28O4/c1-32-27-7-3-5-23(19-27)10-11-24-14-17-28(31)29(20-24)33-26-15-12-21(13-16-26)8-9-22-4-2-6-25(30)18-22/h2-7,12-20,30-31H,8-11H2,1H3
InChI Key NZWFFDGHEUMZNF-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C29H28O4
Molecular Weight 440.50 g/mol
Exact Mass 440.19875937 g/mol
Topological Polar Surface Area (TPSA) 58.90 Ų
XlogP 7.10
Atomic LogP (AlogP) 6.47
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 9

Synonyms

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perrottetin E 11'-methyl ether
Perrottetin E-11'-Methyl Ether
135203-46-2
CHEMBL458919

2D Structure

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2D Structure of Perrottetin E 11'-Methyl Ether

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9356 93.56%
Caco-2 - 0.7614 76.14%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.9103 91.03%
OATP2B1 inhibitior - 0.8559 85.59%
OATP1B1 inhibitior + 0.9105 91.05%
OATP1B3 inhibitior + 0.9504 95.04%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.9588 95.88%
P-glycoprotein inhibitior + 0.9302 93.02%
P-glycoprotein substrate + 0.5545 55.45%
CYP3A4 substrate + 0.5771 57.71%
CYP2C9 substrate - 0.6092 60.92%
CYP2D6 substrate + 0.4547 45.47%
CYP3A4 inhibition - 0.7660 76.60%
CYP2C9 inhibition + 0.8540 85.40%
CYP2C19 inhibition + 0.9145 91.45%
CYP2D6 inhibition - 0.8113 81.13%
CYP1A2 inhibition + 0.8525 85.25%
CYP2C8 inhibition + 0.8866 88.66%
CYP inhibitory promiscuity + 0.7899 78.99%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.7043 70.43%
Carcinogenicity (trinary) Non-required 0.5808 58.08%
Eye corrosion - 0.9424 94.24%
Eye irritation - 0.7271 72.71%
Skin irritation - 0.6544 65.44%
Skin corrosion - 0.8948 89.48%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8477 84.77%
Micronuclear - 0.6441 64.41%
Hepatotoxicity - 0.8074 80.74%
skin sensitisation - 0.8265 82.65%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity - 0.6606 66.06%
Acute Oral Toxicity (c) III 0.7299 72.99%
Estrogen receptor binding + 0.8903 89.03%
Androgen receptor binding + 0.8585 85.85%
Thyroid receptor binding + 0.6829 68.29%
Glucocorticoid receptor binding + 0.7874 78.74%
Aromatase binding - 0.5182 51.82%
PPAR gamma + 0.7640 76.40%
Honey bee toxicity - 0.8155 81.55%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.6600 66.00%
Fish aquatic toxicity + 0.9044 90.44%

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
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 97.34% 96.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.23% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.05% 91.11%
CHEMBL2581 P07339 Cathepsin D 94.45% 98.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.44% 99.15%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.96% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.16% 95.56%
CHEMBL2535 P11166 Glucose transporter 92.98% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.78% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.41% 94.00%
CHEMBL1907 P15144 Aminopeptidase N 89.54% 93.31%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 89.13% 96.95%
CHEMBL4208 P20618 Proteasome component C5 89.12% 90.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 88.42% 95.89%
CHEMBL226 P30542 Adenosine A1 receptor 88.05% 95.93%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 87.63% 86.92%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.98% 95.89%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 86.27% 95.50%
CHEMBL240 Q12809 HERG 85.60% 89.76%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 85.24% 92.67%
CHEMBL5203 P33316 dUTP pyrophosphatase 85.07% 99.18%
CHEMBL3401 O75469 Pregnane X receptor 84.11% 94.73%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.25% 92.62%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.90% 93.99%

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.
Apopellia endiviifolia

Cross-Links

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PubChem 14841123
LOTUS LTS0171737
wikiData Q105188492