4-(4,5-Dimethoxy-2-prop-2-enylphenoxy)-3,4-dimethoxy-6-prop-2-enylcyclohex-2-en-1-one

Details

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Internal ID 92cc4484-0f7f-44a5-aa7c-f7dcb99d6122
Taxonomy Benzenoids > Benzene and substituted derivatives > Methoxybenzenes > Dimethoxybenzenes
IUPAC Name 4-(4,5-dimethoxy-2-prop-2-enylphenoxy)-3,4-dimethoxy-6-prop-2-enylcyclohex-2-en-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H28O6/c1-7-9-15-11-19(24-3)20(25-4)13-18(15)28-22(27-6)14-16(10-8-2)17(23)12-21(22)26-5/h7-8,11-13,16H,1-2,9-10,14H2,3-6H3
InChI Key JYXLTLQGCJMUEX-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H28O6
Molecular Weight 388.50 g/mol
Exact Mass 388.18858861 g/mol
Topological Polar Surface Area (TPSA) 63.20 Ų
XlogP 3.70
Atomic LogP (AlogP) 3.85
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-(4,5-Dimethoxy-2-prop-2-enylphenoxy)-3,4-dimethoxy-6-prop-2-enylcyclohex-2-en-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 + 0.9912 99.12%
Caco-2 + 0.7938 79.38%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.7769 77.69%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7998 79.98%
OATP1B3 inhibitior + 0.9319 93.19%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.9048 90.48%
P-glycoprotein inhibitior + 0.7516 75.16%
P-glycoprotein substrate - 0.5919 59.19%
CYP3A4 substrate + 0.6021 60.21%
CYP2C9 substrate - 0.8031 80.31%
CYP2D6 substrate - 0.8011 80.11%
CYP3A4 inhibition + 0.5706 57.06%
CYP2C9 inhibition - 0.8836 88.36%
CYP2C19 inhibition + 0.6843 68.43%
CYP2D6 inhibition - 0.9238 92.38%
CYP1A2 inhibition - 0.5083 50.83%
CYP2C8 inhibition - 0.5808 58.08%
CYP inhibitory promiscuity + 0.6440 64.40%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7832 78.32%
Carcinogenicity (trinary) Non-required 0.6522 65.22%
Eye corrosion - 0.9697 96.97%
Eye irritation - 0.9032 90.32%
Skin irritation - 0.7778 77.78%
Skin corrosion - 0.9827 98.27%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7723 77.23%
Micronuclear - 0.6282 62.82%
Hepatotoxicity + 0.6017 60.17%
skin sensitisation - 0.7447 74.47%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity + 0.6627 66.27%
Acute Oral Toxicity (c) III 0.5773 57.73%
Estrogen receptor binding + 0.7682 76.82%
Androgen receptor binding + 0.5518 55.18%
Thyroid receptor binding + 0.7709 77.09%
Glucocorticoid receptor binding + 0.7692 76.92%
Aromatase binding + 0.6453 64.53%
PPAR gamma + 0.6059 60.59%
Honey bee toxicity - 0.6325 63.25%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9950 99.50%

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 98.03% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.18% 96.09%
CHEMBL1937 Q92769 Histone deacetylase 2 93.79% 94.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.73% 95.56%
CHEMBL2581 P07339 Cathepsin D 92.97% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.21% 97.25%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 86.95% 91.07%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.47% 95.89%
CHEMBL5925 P22413 Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 85.88% 92.38%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.66% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.57% 86.33%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.52% 92.94%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.29% 93.99%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.44% 92.62%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.91% 96.00%
CHEMBL4530 P00488 Coagulation factor XIII 81.06% 96.00%
CHEMBL1902 P62942 FK506-binding protein 1A 80.60% 97.05%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 80.33% 93.40%
CHEMBL1871 P10275 Androgen Receptor 80.20% 96.43%
CHEMBL3524 P56524 Histone deacetylase 4 80.13% 92.97%

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.
Aniba lancifolia

Cross-Links

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PubChem 163062192
LOTUS LTS0139068
wikiData Q104170014