1,4-Bis(3,4-dimethoxyphenyl)-2,3-dimethylbutan-1-one

Details

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Internal ID ea26853a-889a-4a73-87d8-fc87dc678b9f
Taxonomy Lignans, neolignans and related compounds > Dibenzylbutane lignans
IUPAC Name 1,4-bis(3,4-dimethoxyphenyl)-2,3-dimethylbutan-1-one
SMILES (Canonical) CC(CC1=CC(=C(C=C1)OC)OC)C(C)C(=O)C2=CC(=C(C=C2)OC)OC
SMILES (Isomeric) CC(CC1=CC(=C(C=C1)OC)OC)C(C)C(=O)C2=CC(=C(C=C2)OC)OC
InChI InChI=1S/C22H28O5/c1-14(11-16-7-9-18(24-3)20(12-16)26-5)15(2)22(23)17-8-10-19(25-4)21(13-17)27-6/h7-10,12-15H,11H2,1-6H3
InChI Key SRJOMSFZTGEQFM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H28O5
Molecular Weight 372.50 g/mol
Exact Mass 372.19367399 g/mol
Topological Polar Surface Area (TPSA) 54.00 Ų
XlogP 4.70
Atomic LogP (AlogP) 4.42
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 1,4-Bis(3,4-dimethoxyphenyl)-2,3-dimethylbutan-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9967 99.67%
Caco-2 + 0.8507 85.07%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.8389 83.89%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9021 90.21%
OATP1B3 inhibitior + 0.9440 94.40%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.8316 83.16%
P-glycoprotein inhibitior + 0.8655 86.55%
P-glycoprotein substrate - 0.6099 60.99%
CYP3A4 substrate - 0.5746 57.46%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7007 70.07%
CYP3A4 inhibition - 0.6392 63.92%
CYP2C9 inhibition - 0.8066 80.66%
CYP2C19 inhibition + 0.7289 72.89%
CYP2D6 inhibition - 0.7553 75.53%
CYP1A2 inhibition + 0.8793 87.93%
CYP2C8 inhibition + 0.7029 70.29%
CYP inhibitory promiscuity + 0.6588 65.88%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7460 74.60%
Carcinogenicity (trinary) Non-required 0.5844 58.44%
Eye corrosion - 0.9485 94.85%
Eye irritation - 0.7983 79.83%
Skin irritation - 0.8421 84.21%
Skin corrosion - 0.9869 98.69%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8798 87.98%
Micronuclear - 0.6941 69.41%
Hepatotoxicity - 0.5216 52.16%
skin sensitisation - 0.8999 89.99%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity - 0.7925 79.25%
Acute Oral Toxicity (c) III 0.7539 75.39%
Estrogen receptor binding + 0.8873 88.73%
Androgen receptor binding + 0.5281 52.81%
Thyroid receptor binding + 0.5954 59.54%
Glucocorticoid receptor binding + 0.7578 75.78%
Aromatase binding + 0.6669 66.69%
PPAR gamma + 0.6918 69.18%
Honey bee toxicity - 0.9505 95.05%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.6101 61.01%
Fish aquatic toxicity + 0.9939 99.39%

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 97.01% 96.09%
CHEMBL1255126 O15151 Protein Mdm4 96.38% 90.20%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.44% 99.17%
CHEMBL2535 P11166 Glucose transporter 94.10% 98.75%
CHEMBL2581 P07339 Cathepsin D 93.20% 98.95%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 92.07% 100.00%
CHEMBL4208 P20618 Proteasome component C5 91.14% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.66% 86.33%
CHEMBL1907588 P02708 Acetylcholine receptor; alpha1/beta1/delta/gamma 89.21% 98.33%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.99% 95.50%
CHEMBL3492 P49721 Proteasome Macropain subunit 83.98% 90.24%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.08% 95.89%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.23% 96.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.69% 90.71%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.49% 95.89%

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.
Nectandra puberula
Virola elongata

Cross-Links

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PubChem 14655047
LOTUS LTS0114241
wikiData Q104197573