4,6-Dimethyl-5-(2-methoxyphenethyl)resorcinol

Details

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Internal ID 8d48573d-952d-49f3-a9bd-83cb5e68f610
Taxonomy Phenylpropanoids and polyketides > Stilbenes
IUPAC Name 5-[2-(2-methoxyphenyl)ethyl]-4,6-dimethylbenzene-1,3-diol
SMILES (Canonical) CC1=C(C(=C(C=C1O)O)C)CCC2=CC=CC=C2OC
SMILES (Isomeric) CC1=C(C(=C(C=C1O)O)C)CCC2=CC=CC=C2OC
InChI InChI=1S/C17H20O3/c1-11-14(12(2)16(19)10-15(11)18)9-8-13-6-4-5-7-17(13)20-3/h4-7,10,18-19H,8-9H2,1-3H3
InChI Key WEJBPOPAORGHIX-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H20O3
Molecular Weight 272.34 g/mol
Exact Mass 272.14124450 g/mol
Topological Polar Surface Area (TPSA) 49.70 Ų
XlogP 4.10
Atomic LogP (AlogP) 3.51
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4,6-Dimethyl-5-(2-methoxyphenethyl)resorcinol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9690 96.90%
Caco-2 + 0.9030 90.30%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.8436 84.36%
OATP2B1 inhibitior - 0.8481 84.81%
OATP1B1 inhibitior + 0.8892 88.92%
OATP1B3 inhibitior + 0.8995 89.95%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.7126 71.26%
P-glycoprotein inhibitior - 0.8408 84.08%
P-glycoprotein substrate - 0.8130 81.30%
CYP3A4 substrate - 0.5255 52.55%
CYP2C9 substrate - 0.5890 58.90%
CYP2D6 substrate + 0.4683 46.83%
CYP3A4 inhibition - 0.7314 73.14%
CYP2C9 inhibition + 0.5491 54.91%
CYP2C19 inhibition + 0.8109 81.09%
CYP2D6 inhibition - 0.7176 71.76%
CYP1A2 inhibition + 0.6501 65.01%
CYP2C8 inhibition + 0.6043 60.43%
CYP inhibitory promiscuity + 0.8421 84.21%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7434 74.34%
Carcinogenicity (trinary) Non-required 0.7034 70.34%
Eye corrosion - 0.9689 96.89%
Eye irritation + 0.5553 55.53%
Skin irritation - 0.6905 69.05%
Skin corrosion - 0.7497 74.97%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8683 86.83%
Micronuclear - 0.7600 76.00%
Hepatotoxicity + 0.5031 50.31%
skin sensitisation - 0.7945 79.45%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.6444 64.44%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity - 0.7958 79.58%
Acute Oral Toxicity (c) III 0.6907 69.07%
Estrogen receptor binding + 0.8588 85.88%
Androgen receptor binding + 0.5445 54.45%
Thyroid receptor binding + 0.6505 65.05%
Glucocorticoid receptor binding + 0.6383 63.83%
Aromatase binding + 0.5669 56.69%
PPAR gamma + 0.7450 74.50%
Honey bee toxicity - 0.9270 92.70%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.9570 95.70%

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 96.97% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.03% 86.33%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 92.11% 89.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.09% 95.56%
CHEMBL2535 P11166 Glucose transporter 89.51% 98.75%
CHEMBL2581 P07339 Cathepsin D 89.38% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.03% 96.09%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.19% 93.99%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.83% 94.00%
CHEMBL1255126 O15151 Protein Mdm4 85.50% 90.20%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.40% 96.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.37% 96.00%
CHEMBL4208 P20618 Proteasome component C5 83.31% 90.00%
CHEMBL240 Q12809 HERG 82.80% 89.76%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.37% 99.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.55% 95.50%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.21% 92.62%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 24796847
NPASS NPC74447