2,3,5-Trimethoxy-6-(1-Propenyl)-2,5-Cyclohexadiene-1,4-Dione

Details

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Internal ID a3af9c88-2999-4a29-9fa5-2d9a4b1509d0
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Quinone and hydroquinone lipids > Prenylquinones > Ubiquinones
IUPAC Name 2,3,5-trimethoxy-6-[(E)-prop-1-enyl]cyclohexa-2,5-diene-1,4-dione
SMILES (Canonical) CC=CC1=C(C(=O)C(=C(C1=O)OC)OC)OC
SMILES (Isomeric) C/C=C/C1=C(C(=O)C(=C(C1=O)OC)OC)OC
InChI InChI=1S/C12H14O5/c1-5-6-7-8(13)11(16-3)12(17-4)9(14)10(7)15-2/h5-6H,1-4H3/b6-5+
InChI Key RTBKABKNDSZTIA-AATRIKPKSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C12H14O5
Molecular Weight 238.24 g/mol
Exact Mass 238.08412354 g/mol
Topological Polar Surface Area (TPSA) 61.80 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.12
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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2,3,5-Trimethoxy-6-(1-propenyl)-2,5-cyclohexadiene-1,4-dione
2,3,5-trimethoxy-6-[(E)-prop-1-enyl]cyclohexa-2,5-diene-1,4-dione

2D Structure

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2D Structure of 2,3,5-Trimethoxy-6-(1-Propenyl)-2,5-Cyclohexadiene-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 + 0.9886 98.86%
Caco-2 + 0.5190 51.90%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Mitochondria 0.8070 80.70%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9184 91.84%
OATP1B3 inhibitior + 0.9736 97.36%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7355 73.55%
P-glycoprotein inhibitior - 0.9248 92.48%
P-glycoprotein substrate - 0.9501 95.01%
CYP3A4 substrate - 0.6479 64.79%
CYP2C9 substrate - 0.6056 60.56%
CYP2D6 substrate - 0.8611 86.11%
CYP3A4 inhibition - 0.8279 82.79%
CYP2C9 inhibition - 0.9627 96.27%
CYP2C19 inhibition - 0.7440 74.40%
CYP2D6 inhibition - 0.9117 91.17%
CYP1A2 inhibition - 0.8068 80.68%
CYP2C8 inhibition - 0.9701 97.01%
CYP inhibitory promiscuity - 0.7461 74.61%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7068 70.68%
Carcinogenicity (trinary) Non-required 0.6272 62.72%
Eye corrosion - 0.8302 83.02%
Eye irritation + 0.8714 87.14%
Skin irritation - 0.6691 66.91%
Skin corrosion - 0.9809 98.09%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5611 56.11%
Micronuclear + 0.6100 61.00%
Hepatotoxicity + 0.7750 77.50%
skin sensitisation - 0.6382 63.82%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity + 0.7289 72.89%
Acute Oral Toxicity (c) III 0.3516 35.16%
Estrogen receptor binding - 0.5958 59.58%
Androgen receptor binding - 0.6871 68.71%
Thyroid receptor binding - 0.6789 67.89%
Glucocorticoid receptor binding - 0.8383 83.83%
Aromatase binding - 0.7243 72.43%
PPAR gamma - 0.7349 73.49%
Honey bee toxicity - 0.7497 74.97%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.8730 87.30%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.96% 95.56%
CHEMBL2581 P07339 Cathepsin D 89.39% 98.95%
CHEMBL1937 Q92769 Histone deacetylase 2 86.07% 94.75%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.68% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.80% 94.45%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.37% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.35% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 80.10% 94.73%

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.
Smirnowia turkestana

Cross-Links

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PubChem 10868332
LOTUS LTS0109893
wikiData Q105245037