2,4,6-Tris[(4-hydroxyphenyl)methyl]-3-methoxy-5-[2-(3-methoxyphenyl)ethyl]phenol

Details

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Internal ID 80ffef70-e00e-45a1-af75-54b007634416
Taxonomy Phenylpropanoids and polyketides > Diarylheptanoids > Linear diarylheptanoids > Curcuminoids
IUPAC Name 2,4,6-tris[(4-hydroxyphenyl)methyl]-3-methoxy-5-[2-(3-methoxyphenyl)ethyl]phenol
SMILES (Canonical) COC1=CC=CC(=C1)CCC2=C(C(=C(C(=C2CC3=CC=C(C=C3)O)OC)CC4=CC=C(C=C4)O)O)CC5=CC=C(C=C5)O
SMILES (Isomeric) COC1=CC=CC(=C1)CCC2=C(C(=C(C(=C2CC3=CC=C(C=C3)O)OC)CC4=CC=C(C=C4)O)O)CC5=CC=C(C=C5)O
InChI InChI=1S/C37H36O6/c1-42-31-5-3-4-24(20-31)12-19-32-33(21-25-6-13-28(38)14-7-25)36(41)35(23-27-10-17-30(40)18-11-27)37(43-2)34(32)22-26-8-15-29(39)16-9-26/h3-11,13-18,20,38-41H,12,19,21-23H2,1-2H3
InChI Key XUTNHXAHBYFBOF-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C37H36O6
Molecular Weight 576.70 g/mol
Exact Mass 576.25118886 g/mol
Topological Polar Surface Area (TPSA) 99.40 Ų
XlogP 8.40
Atomic LogP (AlogP) 7.08
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 11

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,4,6-Tris[(4-hydroxyphenyl)methyl]-3-methoxy-5-[2-(3-methoxyphenyl)ethyl]phenol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9654 96.54%
Caco-2 - 0.6964 69.64%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.9525 95.25%
OATP2B1 inhibitior - 0.8569 85.69%
OATP1B1 inhibitior + 0.7738 77.38%
OATP1B3 inhibitior + 0.9192 91.92%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9884 98.84%
P-glycoprotein inhibitior + 0.9206 92.06%
P-glycoprotein substrate + 0.5548 55.48%
CYP3A4 substrate + 0.5706 57.06%
CYP2C9 substrate - 0.6120 61.20%
CYP2D6 substrate + 0.5079 50.79%
CYP3A4 inhibition - 0.7202 72.02%
CYP2C9 inhibition - 0.5824 58.24%
CYP2C19 inhibition + 0.7466 74.66%
CYP2D6 inhibition - 0.7948 79.48%
CYP1A2 inhibition + 0.7322 73.22%
CYP2C8 inhibition + 0.8732 87.32%
CYP inhibitory promiscuity + 0.6519 65.19%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.6654 66.54%
Carcinogenicity (trinary) Non-required 0.7043 70.43%
Eye corrosion - 0.9744 97.44%
Eye irritation - 0.7500 75.00%
Skin irritation - 0.7994 79.94%
Skin corrosion - 0.8856 88.56%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9431 94.31%
Micronuclear - 0.7500 75.00%
Hepatotoxicity - 0.7625 76.25%
skin sensitisation - 0.8487 84.87%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.8641 86.41%
Acute Oral Toxicity (c) III 0.6511 65.11%
Estrogen receptor binding + 0.8996 89.96%
Androgen receptor binding + 0.8653 86.53%
Thyroid receptor binding + 0.7125 71.25%
Glucocorticoid receptor binding + 0.8360 83.60%
Aromatase binding - 0.4931 49.31%
PPAR gamma + 0.7555 75.55%
Honey bee toxicity - 0.8083 80.83%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.9894 98.94%

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 96.68% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.17% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.71% 96.09%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 92.54% 95.50%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.37% 94.00%
CHEMBL2535 P11166 Glucose transporter 91.15% 98.75%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.07% 99.15%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.70% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.58% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.42% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.66% 95.56%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 87.67% 95.17%
CHEMBL235 P37231 Peroxisome proliferator-activated receptor gamma 87.06% 95.39%
CHEMBL3401 O75469 Pregnane X receptor 86.82% 94.73%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 86.15% 95.89%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.12% 95.89%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 84.90% 86.92%
CHEMBL4208 P20618 Proteasome component C5 82.52% 90.00%
CHEMBL5203 P33316 dUTP pyrophosphatase 82.19% 99.18%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.08% 96.95%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 80.93% 91.71%
CHEMBL4101 P17612 cAMP-dependent protein kinase alpha-catalytic subunit 80.38% 82.86%

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.
Bletilla striata
Syzygium aromaticum

Cross-Links

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PubChem 101845671
NPASS NPC190981
LOTUS LTS0246274
wikiData Q105342574