2,4,3',5'-Tetrahydroxy-4'(3,7-di-methyl-2,6-octadienyl)-stilbene

Details

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Internal ID 84226fdf-a561-42a0-8cd7-bf1b8b15a7e1
Taxonomy Phenylpropanoids and polyketides > Stilbenes
IUPAC Name 5-[2-(2,4-dihydroxyphenyl)ethenyl]-2-(3,7-dimethylocta-2,6-dienyl)benzene-1,3-diol
SMILES (Canonical) CC(=CCCC(=CCC1=C(C=C(C=C1O)C=CC2=C(C=C(C=C2)O)O)O)C)C
SMILES (Isomeric) CC(=CCCC(=CCC1=C(C=C(C=C1O)C=CC2=C(C=C(C=C2)O)O)O)C)C
InChI InChI=1S/C24H28O4/c1-16(2)5-4-6-17(3)7-12-21-23(27)13-18(14-24(21)28)8-9-19-10-11-20(25)15-22(19)26/h5,7-11,13-15,25-28H,4,6,12H2,1-3H3
InChI Key OEILZVSHVTYHKL-UHFFFAOYSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C24H28O4
Molecular Weight 380.50 g/mol
Exact Mass 380.19875937 g/mol
Topological Polar Surface Area (TPSA) 80.90 Ų
XlogP 6.60
Atomic LogP (AlogP) 5.91
H-Bond Acceptor 4
H-Bond Donor 4
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,4,3',5'-Tetrahydroxy-4'(3,7-di-methyl-2,6-octadienyl)-stilbene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9902 99.02%
Caco-2 - 0.5949 59.49%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.7958 79.58%
OATP2B1 inhibitior + 0.5739 57.39%
OATP1B1 inhibitior + 0.8499 84.99%
OATP1B3 inhibitior + 0.8852 88.52%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.9737 97.37%
P-glycoprotein inhibitior + 0.6146 61.46%
P-glycoprotein substrate - 0.8270 82.70%
CYP3A4 substrate - 0.5133 51.33%
CYP2C9 substrate - 0.6075 60.75%
CYP2D6 substrate - 0.6697 66.97%
CYP3A4 inhibition + 0.7106 71.06%
CYP2C9 inhibition + 0.6642 66.42%
CYP2C19 inhibition + 0.6617 66.17%
CYP2D6 inhibition - 0.7716 77.16%
CYP1A2 inhibition + 0.7513 75.13%
CYP2C8 inhibition + 0.5791 57.91%
CYP inhibitory promiscuity + 0.7917 79.17%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7962 79.62%
Carcinogenicity (trinary) Non-required 0.7502 75.02%
Eye corrosion - 0.9868 98.68%
Eye irritation - 0.6471 64.71%
Skin irritation - 0.7824 78.24%
Skin corrosion - 0.8587 85.87%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7731 77.31%
Micronuclear - 0.8700 87.00%
Hepatotoxicity - 0.6675 66.75%
skin sensitisation - 0.5300 53.00%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity - 0.7040 70.40%
Acute Oral Toxicity (c) III 0.6090 60.90%
Estrogen receptor binding + 0.9270 92.70%
Androgen receptor binding + 0.9019 90.19%
Thyroid receptor binding + 0.7367 73.67%
Glucocorticoid receptor binding + 0.8723 87.23%
Aromatase binding + 0.7904 79.04%
PPAR gamma + 0.9375 93.75%
Honey bee toxicity - 0.8701 87.01%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 1.0000 100.00%

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 98.57% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.10% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 94.78% 94.73%
CHEMBL1951 P21397 Monoamine oxidase A 93.71% 91.49%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 90.14% 93.10%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.01% 96.00%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 89.85% 92.08%
CHEMBL3194 P02766 Transthyretin 88.84% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.87% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.92% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.04% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.42% 99.17%
CHEMBL4208 P20618 Proteasome component C5 81.30% 90.00%
CHEMBL3038469 P24941 CDK2/Cyclin A 80.38% 91.38%

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.
Artocarpus altilis
Milicia excelsa

Cross-Links

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PubChem 174858
LOTUS LTS0016838
wikiData Q105190303