2-[3-(3,4-Dimethoxyphenyl)propyl]-1,3,5-trimethoxybenzene

Details

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Internal ID 7a7bd65f-c62b-4c78-b5d9-edc249a33090
Taxonomy Phenylpropanoids and polyketides > Linear 1,3-diarylpropanoids
IUPAC Name 2-[3-(3,4-dimethoxyphenyl)propyl]-1,3,5-trimethoxybenzene
SMILES (Canonical) COC1=C(C=C(C=C1)CCCC2=C(C=C(C=C2OC)OC)OC)OC
SMILES (Isomeric) COC1=C(C=C(C=C1)CCCC2=C(C=C(C=C2OC)OC)OC)OC
InChI InChI=1S/C20H26O5/c1-21-15-12-18(23-3)16(19(13-15)24-4)8-6-7-14-9-10-17(22-2)20(11-14)25-5/h9-13H,6-8H2,1-5H3
InChI Key BSSWLCWIFXNYDF-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H26O5
Molecular Weight 346.40 g/mol
Exact Mass 346.17802393 g/mol
Topological Polar Surface Area (TPSA) 46.20 Ų
XlogP 4.10
Atomic LogP (AlogP) 3.90
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-[3-(3,4-Dimethoxyphenyl)propyl]-1,3,5-trimethoxybenzene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9881 98.81%
Caco-2 + 0.9569 95.69%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.8502 85.02%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8705 87.05%
OATP1B3 inhibitior + 0.9519 95.19%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.5738 57.38%
P-glycoprotein inhibitior + 0.7258 72.58%
P-glycoprotein substrate - 0.5801 58.01%
CYP3A4 substrate + 0.5168 51.68%
CYP2C9 substrate - 0.5942 59.42%
CYP2D6 substrate + 0.5275 52.75%
CYP3A4 inhibition - 0.8145 81.45%
CYP2C9 inhibition - 0.7933 79.33%
CYP2C19 inhibition + 0.7618 76.18%
CYP2D6 inhibition - 0.9142 91.42%
CYP1A2 inhibition + 0.7566 75.66%
CYP2C8 inhibition + 0.8724 87.24%
CYP inhibitory promiscuity + 0.8005 80.05%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7143 71.43%
Carcinogenicity (trinary) Non-required 0.5713 57.13%
Eye corrosion - 0.9415 94.15%
Eye irritation - 0.6352 63.52%
Skin irritation - 0.8333 83.33%
Skin corrosion - 0.9676 96.76%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8510 85.10%
Micronuclear - 0.7267 72.67%
Hepatotoxicity - 0.7000 70.00%
skin sensitisation - 0.8801 88.01%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity - 0.7882 78.82%
Acute Oral Toxicity (c) III 0.7657 76.57%
Estrogen receptor binding + 0.8598 85.98%
Androgen receptor binding + 0.5802 58.02%
Thyroid receptor binding + 0.7278 72.78%
Glucocorticoid receptor binding + 0.6382 63.82%
Aromatase binding - 0.6621 66.21%
PPAR gamma - 0.5883 58.83%
Honey bee toxicity - 0.9306 93.06%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6500 65.00%
Fish aquatic toxicity + 0.9356 93.56%

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
CHEMBL240 Q12809 HERG 97.24% 89.76%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.31% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.58% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.10% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.15% 99.17%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 87.46% 95.17%
CHEMBL2535 P11166 Glucose transporter 86.80% 98.75%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.45% 93.99%
CHEMBL1255126 O15151 Protein Mdm4 85.38% 90.20%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.35% 94.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.25% 95.89%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.50% 92.94%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.46% 96.00%
CHEMBL4208 P20618 Proteasome component C5 84.39% 90.00%
CHEMBL3492 P49721 Proteasome Macropain subunit 84.28% 90.24%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.25% 95.56%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.62% 96.95%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.25% 95.50%

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.
Litsea hypophaea

Cross-Links

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PubChem 71229208
LOTUS LTS0188926
wikiData Q104945413