Evofolin B

Details

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Internal ID 7e93f254-cdf0-4cce-840e-91da14e6fd7f
Taxonomy Phenylpropanoids and polyketides > Stilbenes
IUPAC Name 3-hydroxy-1,2-bis(4-hydroxy-3-methoxyphenyl)propan-1-one
SMILES (Canonical) COC1=C(C=CC(=C1)C(CO)C(=O)C2=CC(=C(C=C2)O)OC)O
SMILES (Isomeric) COC1=C(C=CC(=C1)C(CO)C(=O)C2=CC(=C(C=C2)O)OC)O
InChI InChI=1S/C17H18O6/c1-22-15-7-10(3-5-13(15)19)12(9-18)17(21)11-4-6-14(20)16(8-11)23-2/h3-8,12,18-20H,9H2,1-2H3
InChI Key QMYGRGKKZBRZKH-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C17H18O6
Molecular Weight 318.32 g/mol
Exact Mass 318.11033829 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 1.80
Atomic LogP (AlogP) 2.07
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 6

Synonyms

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168254-96-4
3-hydroxy-1,2-bis(4-hydroxy-3-methoxyphenyl)propan-1-one
CHEMBL448601
AKOS032948821

2D Structure

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2D Structure of Evofolin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9820 98.20%
Caco-2 + 0.7119 71.19%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.8890 88.90%
OATP2B1 inhibitior - 0.8474 84.74%
OATP1B1 inhibitior + 0.9217 92.17%
OATP1B3 inhibitior + 0.9157 91.57%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.7603 76.03%
P-glycoprotein inhibitior - 0.7902 79.02%
P-glycoprotein substrate - 0.8130 81.30%
CYP3A4 substrate - 0.6356 63.56%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7492 74.92%
CYP3A4 inhibition - 0.7099 70.99%
CYP2C9 inhibition - 0.7001 70.01%
CYP2C19 inhibition + 0.6754 67.54%
CYP2D6 inhibition - 0.8665 86.65%
CYP1A2 inhibition + 0.7237 72.37%
CYP2C8 inhibition - 0.6401 64.01%
CYP inhibitory promiscuity + 0.6127 61.27%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.7943 79.43%
Carcinogenicity (trinary) Non-required 0.7601 76.01%
Eye corrosion - 0.9700 97.00%
Eye irritation - 0.4842 48.42%
Skin irritation - 0.7644 76.44%
Skin corrosion - 0.9737 97.37%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7887 78.87%
Micronuclear - 0.5141 51.41%
Hepatotoxicity - 0.6875 68.75%
skin sensitisation - 0.7707 77.07%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity - 0.8449 84.49%
Acute Oral Toxicity (c) III 0.7376 73.76%
Estrogen receptor binding + 0.7321 73.21%
Androgen receptor binding + 0.5601 56.01%
Thyroid receptor binding + 0.7963 79.63%
Glucocorticoid receptor binding + 0.7615 76.15%
Aromatase binding - 0.4916 49.16%
PPAR gamma - 0.5373 53.73%
Honey bee toxicity - 0.9443 94.43%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.7415 74.15%
Fish aquatic toxicity + 0.9142 91.42%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.46% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.06% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.77% 99.17%
CHEMBL1255126 O15151 Protein Mdm4 92.44% 90.20%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.96% 86.33%
CHEMBL2535 P11166 Glucose transporter 91.52% 98.75%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 90.51% 100.00%
CHEMBL4208 P20618 Proteasome component C5 90.37% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.15% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.32% 96.00%
CHEMBL1907588 P02708 Acetylcholine receptor; alpha1/beta1/delta/gamma 84.30% 98.33%
CHEMBL2581 P07339 Cathepsin D 84.02% 98.95%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.32% 96.95%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 83.20% 89.62%
CHEMBL3194 P02766 Transthyretin 83.04% 90.71%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.47% 90.71%

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.
Anastatica hierochuntica
Aquilaria sinensis
Carya cathayensis
Couepia ulei
Daphne feddei
Isatis tinctoria
Microtropis japonica
Sida acuta
Tetradium glabrifolium
Zanthoxylum ailanthoides

Cross-Links

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PubChem 5317306
NPASS NPC46161
LOTUS LTS0107561
wikiData Q104399169