2-Hydroxy-3-methoxy-5,6-dimethylcyclohexa-2,5-diene-1,4-dione

Details

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Internal ID 77a47f79-dba4-45b6-8e09-0e0aa02b040a
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Quinone and hydroquinone lipids > Prenylquinones > Ubiquinones
IUPAC Name 2-hydroxy-3-methoxy-5,6-dimethylcyclohexa-2,5-diene-1,4-dione
SMILES (Canonical) CC1=C(C(=O)C(=C(C1=O)O)OC)C
SMILES (Isomeric) CC1=C(C(=O)C(=C(C1=O)O)OC)C
InChI InChI=1S/C9H10O4/c1-4-5(2)7(11)9(13-3)8(12)6(4)10/h12H,1-3H3
InChI Key VWUCKQQFJCJRLY-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C9H10O4
Molecular Weight 182.17 g/mol
Exact Mass 182.05790880 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 0.90
Atomic LogP (AlogP) 0.89
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Hydroxy-3-methoxy-5,6-dimethylcyclohexa-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 + 0.9788 97.88%
Caco-2 - 0.5288 52.88%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.8429 84.29%
Subcellular localzation Mitochondria 0.8276 82.76%
OATP2B1 inhibitior - 0.8613 86.13%
OATP1B1 inhibitior + 0.9415 94.15%
OATP1B3 inhibitior + 0.9633 96.33%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9217 92.17%
P-glycoprotein inhibitior - 0.9393 93.93%
P-glycoprotein substrate - 0.9885 98.85%
CYP3A4 substrate - 0.6217 62.17%
CYP2C9 substrate - 0.7962 79.62%
CYP2D6 substrate - 0.8816 88.16%
CYP3A4 inhibition - 0.8758 87.58%
CYP2C9 inhibition - 0.9653 96.53%
CYP2C19 inhibition - 0.8053 80.53%
CYP2D6 inhibition - 0.8858 88.58%
CYP1A2 inhibition - 0.9055 90.55%
CYP2C8 inhibition - 0.9833 98.33%
CYP inhibitory promiscuity - 0.8932 89.32%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7168 71.68%
Carcinogenicity (trinary) Non-required 0.6382 63.82%
Eye corrosion - 0.8837 88.37%
Eye irritation + 0.8857 88.57%
Skin irritation - 0.5890 58.90%
Skin corrosion - 0.9744 97.44%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6533 65.33%
Micronuclear + 0.5900 59.00%
Hepatotoxicity + 0.6533 65.33%
skin sensitisation - 0.6570 65.70%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity + 0.7200 72.00%
Acute Oral Toxicity (c) III 0.3441 34.41%
Estrogen receptor binding - 0.7127 71.27%
Androgen receptor binding - 0.7370 73.70%
Thyroid receptor binding - 0.6970 69.70%
Glucocorticoid receptor binding - 0.8801 88.01%
Aromatase binding - 0.7843 78.43%
PPAR gamma - 0.8563 85.63%
Honey bee toxicity - 0.9117 91.17%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.8231 82.31%

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 93.59% 95.56%
CHEMBL2581 P07339 Cathepsin D 88.04% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.50% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.76% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 84.21% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.74% 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 136349965
LOTUS LTS0219430
wikiData Q105298281