2,3-Dimethoxy-5-propylcyclohexa-2,5-diene-1,4-dione

Details

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Internal ID aba7db30-f4a7-44b5-be6c-b2362add9a53
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Quinone and hydroquinone lipids > Prenylquinones > Ubiquinones
IUPAC Name 2,3-dimethoxy-5-propylcyclohexa-2,5-diene-1,4-dione
SMILES (Canonical) CCCC1=CC(=O)C(=C(C1=O)OC)OC
SMILES (Isomeric) CCCC1=CC(=O)C(=C(C1=O)OC)OC
InChI InChI=1S/C11H14O4/c1-4-5-7-6-8(12)10(14-2)11(15-3)9(7)13/h6H,4-5H2,1-3H3
InChI Key SJUBXPQMWFESTQ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H14O4
Molecular Weight 210.23 g/mol
Exact Mass 210.08920892 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 1.80
Atomic LogP (AlogP) 1.37
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,3-Dimethoxy-5-propylcyclohexa-2,5-diene-1,4-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9892 98.92%
Caco-2 + 0.8902 89.02%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.7857 78.57%
Subcellular localzation Mitochondria 0.7981 79.81%
OATP2B1 inhibitior - 0.8563 85.63%
OATP1B1 inhibitior + 0.9408 94.08%
OATP1B3 inhibitior + 0.9700 97.00%
MATE1 inhibitior - 0.6800 68.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9111 91.11%
P-glycoprotein inhibitior - 0.9321 93.21%
P-glycoprotein substrate - 0.8522 85.22%
CYP3A4 substrate - 0.6179 61.79%
CYP2C9 substrate - 0.7795 77.95%
CYP2D6 substrate - 0.8653 86.53%
CYP3A4 inhibition - 0.8244 82.44%
CYP2C9 inhibition - 0.8734 87.34%
CYP2C19 inhibition - 0.7157 71.57%
CYP2D6 inhibition - 0.8559 85.59%
CYP1A2 inhibition - 0.7856 78.56%
CYP2C8 inhibition - 0.9489 94.89%
CYP inhibitory promiscuity - 0.7028 70.28%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7140 71.40%
Carcinogenicity (trinary) Non-required 0.5919 59.19%
Eye corrosion - 0.9256 92.56%
Eye irritation + 0.9055 90.55%
Skin irritation - 0.7448 74.48%
Skin corrosion - 0.9763 97.63%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5502 55.02%
Micronuclear - 0.7400 74.00%
Hepatotoxicity + 0.5186 51.86%
skin sensitisation - 0.6271 62.71%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity + 0.6074 60.74%
Acute Oral Toxicity (c) III 0.6716 67.16%
Estrogen receptor binding - 0.6111 61.11%
Androgen receptor binding - 0.6284 62.84%
Thyroid receptor binding - 0.6126 61.26%
Glucocorticoid receptor binding - 0.7776 77.76%
Aromatase binding - 0.8407 84.07%
PPAR gamma - 0.8320 83.20%
Honey bee toxicity - 0.9216 92.16%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9240 92.40%

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
CHEMBL2581 P07339 Cathepsin D 96.69% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.96% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.59% 95.56%
CHEMBL255 P29275 Adenosine A2b receptor 89.84% 98.59%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.16% 86.33%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.63% 97.25%
CHEMBL230 P35354 Cyclooxygenase-2 81.39% 89.63%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.89% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.87% 94.00%

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 12451938
LOTUS LTS0152062
wikiData Q105254553