1-(2,6-Dimethoxyphenyl)-9-(4-methoxyphenyl)nonan-1-one

Details

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Internal ID c5b884a2-542a-4697-8de0-1243795263d9
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name 1-(2,6-dimethoxyphenyl)-9-(4-methoxyphenyl)nonan-1-one
SMILES (Canonical) COC1=CC=C(C=C1)CCCCCCCCC(=O)C2=C(C=CC=C2OC)OC
SMILES (Isomeric) COC1=CC=C(C=C1)CCCCCCCCC(=O)C2=C(C=CC=C2OC)OC
InChI InChI=1S/C24H32O4/c1-26-20-17-15-19(16-18-20)11-8-6-4-5-7-9-12-21(25)24-22(27-2)13-10-14-23(24)28-3/h10,13-18H,4-9,11-12H2,1-3H3
InChI Key DBXOINQVJUWNRR-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C24H32O4
Molecular Weight 384.50 g/mol
Exact Mass 384.23005950 g/mol
Topological Polar Surface Area (TPSA) 44.80 Ų
XlogP 6.50
Atomic LogP (AlogP) 5.87
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 13

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-(2,6-Dimethoxyphenyl)-9-(4-methoxyphenyl)nonan-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 + 0.9957 99.57%
Caco-2 + 0.6410 64.10%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.9411 94.11%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9238 92.38%
OATP1B3 inhibitior + 0.9589 95.89%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.9537 95.37%
P-glycoprotein inhibitior + 0.8836 88.36%
P-glycoprotein substrate - 0.6679 66.79%
CYP3A4 substrate + 0.5623 56.23%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3462 34.62%
CYP3A4 inhibition - 0.5343 53.43%
CYP2C9 inhibition - 0.7127 71.27%
CYP2C19 inhibition + 0.8775 87.75%
CYP2D6 inhibition - 0.8802 88.02%
CYP1A2 inhibition + 0.8411 84.11%
CYP2C8 inhibition + 0.5930 59.30%
CYP inhibitory promiscuity + 0.6668 66.68%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7554 75.54%
Carcinogenicity (trinary) Non-required 0.7100 71.00%
Eye corrosion - 0.9692 96.92%
Eye irritation - 0.8107 81.07%
Skin irritation - 0.9036 90.36%
Skin corrosion - 0.9854 98.54%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9430 94.30%
Micronuclear - 0.7626 76.26%
Hepatotoxicity - 0.6947 69.47%
skin sensitisation - 0.9519 95.19%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity - 0.6063 60.63%
Acute Oral Toxicity (c) III 0.6158 61.58%
Estrogen receptor binding + 0.7922 79.22%
Androgen receptor binding + 0.7991 79.91%
Thyroid receptor binding + 0.6497 64.97%
Glucocorticoid receptor binding + 0.5643 56.43%
Aromatase binding + 0.5957 59.57%
PPAR gamma + 0.5533 55.33%
Honey bee toxicity - 0.9316 93.16%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.5076 50.76%
Fish aquatic toxicity + 0.9839 98.39%

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 98.74% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.20% 99.17%
CHEMBL3492 P49721 Proteasome Macropain subunit 93.81% 90.24%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.32% 95.56%
CHEMBL2581 P07339 Cathepsin D 93.25% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.48% 86.33%
CHEMBL2535 P11166 Glucose transporter 90.90% 98.75%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 90.87% 95.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 90.37% 95.50%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.24% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 88.55% 96.00%
CHEMBL1255126 O15151 Protein Mdm4 88.34% 90.20%
CHEMBL1907 P15144 Aminopeptidase N 87.84% 93.31%
CHEMBL4208 P20618 Proteasome component C5 85.43% 90.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.13% 96.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.45% 94.00%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 80.80% 92.08%

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.
Myristica fragrans

Cross-Links

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PubChem 13965863
LOTUS LTS0055718
wikiData Q104975019