Simonsinol

Details

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Internal ID 79d0e8fb-e0f3-4133-b9ae-7e9c75bf6f67
Taxonomy Benzenoids > Benzene and substituted derivatives > Terphenyls > M-terphenyls
IUPAC Name 2-(2-hydroxy-5-prop-2-enylphenyl)-6-(4-hydroxy-3-prop-2-enylphenyl)-4-prop-2-enylphenol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H26O3/c1-4-7-18-10-12-26(29)23(14-18)24-16-19(8-5-2)15-22(27(24)30)20-11-13-25(28)21(17-20)9-6-3/h4-6,10-17,28-30H,1-3,7-9H2
InChI Key FAERQKZGOCHVNC-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C27H26O3
Molecular Weight 398.50 g/mol
Exact Mass 398.18819469 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 7.30
Atomic LogP (AlogP) 6.32
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 8

Synonyms

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155709-40-3
Simonsil
2-(2-hydroxy-5-prop-2-enylphenyl)-6-(4-hydroxy-3-prop-2-enylphenyl)-4-prop-2-enylphenol
3'',5,5'-Triallyl-[1,1':3',1''-terphenyl]-2,2',4''-triol
AKOS032962361
FS-10428

2D Structure

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2D Structure of Simonsinol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9953 99.53%
Caco-2 - 0.8593 85.93%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.8700 87.00%
OATP2B1 inhibitior + 0.5730 57.30%
OATP1B1 inhibitior + 0.8738 87.38%
OATP1B3 inhibitior + 0.8185 81.85%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.8389 83.89%
P-glycoprotein inhibitior - 0.4385 43.85%
P-glycoprotein substrate - 0.8614 86.14%
CYP3A4 substrate - 0.5630 56.30%
CYP2C9 substrate - 0.8060 80.60%
CYP2D6 substrate + 0.4276 42.76%
CYP3A4 inhibition - 0.6583 65.83%
CYP2C9 inhibition + 0.8030 80.30%
CYP2C19 inhibition + 0.8974 89.74%
CYP2D6 inhibition - 0.9217 92.17%
CYP1A2 inhibition + 0.5480 54.80%
CYP2C8 inhibition + 0.8076 80.76%
CYP inhibitory promiscuity + 0.8758 87.58%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6485 64.85%
Carcinogenicity (trinary) Non-required 0.6014 60.14%
Eye corrosion - 0.9554 95.54%
Eye irritation - 0.6153 61.53%
Skin irritation - 0.6024 60.24%
Skin corrosion - 0.8574 85.74%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7494 74.94%
Micronuclear + 0.5400 54.00%
Hepatotoxicity + 0.8000 80.00%
skin sensitisation + 0.8317 83.17%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity - 0.8214 82.14%
Acute Oral Toxicity (c) III 0.7286 72.86%
Estrogen receptor binding + 0.7870 78.70%
Androgen receptor binding + 0.8242 82.42%
Thyroid receptor binding + 0.6864 68.64%
Glucocorticoid receptor binding + 0.7888 78.88%
Aromatase binding + 0.7951 79.51%
PPAR gamma + 0.9060 90.60%
Honey bee toxicity - 0.7390 73.90%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9966 99.66%

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
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 98.31% 95.17%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 98.23% 83.57%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.29% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 97.08% 91.49%
CHEMBL2581 P07339 Cathepsin D 96.68% 98.95%
CHEMBL3194 P02766 Transthyretin 88.94% 90.71%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 88.26% 95.50%
CHEMBL3492 P49721 Proteasome Macropain subunit 87.51% 90.24%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 87.05% 99.15%
CHEMBL1929 P47989 Xanthine dehydrogenase 86.26% 96.12%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.22% 86.33%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 85.66% 98.11%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 84.92% 91.71%
CHEMBL2216739 Q92523 Carnitine O-palmitoyltransferase 1, muscle isoform 84.84% 88.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.13% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.46% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 83.23% 94.73%
CHEMBL3230 O95977 Sphingosine 1-phosphate receptor Edg-6 80.54% 94.01%

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.
Illicium simonsii

Cross-Links

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PubChem 10340821
LOTUS LTS0227444
wikiData Q104992204