5-(3-Hydroxybutan-2-yl)-2,3-dimethoxycyclohexa-2,5-diene-1,4-dione

Details

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Internal ID b8bf8064-ccd5-431c-bbbe-692c3eddb3cc
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Quinone and hydroquinone lipids > Prenylquinones > Ubiquinones
IUPAC Name 5-(3-hydroxybutan-2-yl)-2,3-dimethoxycyclohexa-2,5-diene-1,4-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H16O5/c1-6(7(2)13)8-5-9(14)11(16-3)12(17-4)10(8)15/h5-7,13H,1-4H3
InChI Key JAQXBCCCRCNHFC-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C12H16O5
Molecular Weight 240.25 g/mol
Exact Mass 240.09977361 g/mol
Topological Polar Surface Area (TPSA) 72.80 Ų
XlogP 0.80
Atomic LogP (AlogP) 0.59
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-(3-Hydroxybutan-2-yl)-2,3-dimethoxycyclohexa-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 + 0.6466 64.66%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.8276 82.76%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9585 95.85%
OATP1B3 inhibitior + 0.9633 96.33%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9172 91.72%
P-glycoprotein inhibitior - 0.9245 92.45%
P-glycoprotein substrate - 0.9274 92.74%
CYP3A4 substrate - 0.6422 64.22%
CYP2C9 substrate - 0.5973 59.73%
CYP2D6 substrate - 0.8757 87.57%
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 - 0.9875 98.75%
CYP inhibitory promiscuity - 0.8932 89.32%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7168 71.68%
Carcinogenicity (trinary) Non-required 0.6382 63.82%
Eye corrosion - 0.8837 88.37%
Eye irritation - 0.7248 72.48%
Skin irritation - 0.5890 58.90%
Skin corrosion - 0.9744 97.44%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5760 57.60%
Micronuclear + 0.5900 59.00%
Hepatotoxicity + 0.5408 54.08%
skin sensitisation - 0.6570 65.70%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity + 0.5543 55.43%
Acute Oral Toxicity (c) III 0.3441 34.41%
Estrogen receptor binding - 0.6139 61.39%
Androgen receptor binding - 0.6287 62.87%
Thyroid receptor binding - 0.6559 65.59%
Glucocorticoid receptor binding - 0.7320 73.20%
Aromatase binding - 0.8446 84.46%
PPAR gamma - 0.7081 70.81%
Honey bee toxicity - 0.8835 88.35%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7600 76.00%
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
CHEMBL2581 P07339 Cathepsin D 96.60% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.66% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.10% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.29% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.43% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.17% 91.11%
CHEMBL2535 P11166 Glucose transporter 80.48% 98.75%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 80.25% 93.03%
CHEMBL1937 Q92769 Histone deacetylase 2 80.11% 94.75%

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 11276501
LOTUS LTS0051278
wikiData Q104169339