3-Hydroxy-2-methyl-5-(3-methylbut-2-enyl)cyclohexa-2,5-diene-1,4-dione

Details

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Internal ID 4e2d1c8d-3bb8-47d3-9c53-90058deb9694
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Quinone and hydroquinone lipids > Prenylquinones
IUPAC Name 3-hydroxy-2-methyl-5-(3-methylbut-2-enyl)cyclohexa-2,5-diene-1,4-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H14O3/c1-7(2)4-5-9-6-10(13)8(3)11(14)12(9)15/h4,6,14H,5H2,1-3H3
InChI Key ZWBAUTGNDSDRLF-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C12H14O3
Molecular Weight 206.24 g/mol
Exact Mass 206.094294304 g/mol
Topological Polar Surface Area (TPSA) 54.40 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.25
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-Hydroxy-2-methyl-5-(3-methylbut-2-enyl)cyclohexa-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 + 0.9902 99.02%
Caco-2 + 0.7878 78.78%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.8468 84.68%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9154 91.54%
OATP1B3 inhibitior + 0.9558 95.58%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8180 81.80%
P-glycoprotein inhibitior - 0.9664 96.64%
P-glycoprotein substrate - 0.9405 94.05%
CYP3A4 substrate - 0.5793 57.93%
CYP2C9 substrate - 0.7931 79.31%
CYP2D6 substrate - 0.8700 87.00%
CYP3A4 inhibition - 0.8599 85.99%
CYP2C9 inhibition - 0.6806 68.06%
CYP2C19 inhibition - 0.7120 71.20%
CYP2D6 inhibition - 0.7542 75.42%
CYP1A2 inhibition - 0.7876 78.76%
CYP2C8 inhibition - 0.9774 97.74%
CYP inhibitory promiscuity - 0.7460 74.60%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.7061 70.61%
Carcinogenicity (trinary) Non-required 0.6788 67.88%
Eye corrosion - 0.8842 88.42%
Eye irritation + 0.8964 89.64%
Skin irritation + 0.6209 62.09%
Skin corrosion - 0.8017 80.17%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6667 66.67%
Micronuclear - 0.6500 65.00%
Hepatotoxicity + 0.5696 56.96%
skin sensitisation + 0.6453 64.53%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity + 0.6282 62.82%
Acute Oral Toxicity (c) III 0.5430 54.30%
Estrogen receptor binding - 0.6499 64.99%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding - 0.7788 77.88%
Glucocorticoid receptor binding - 0.5056 50.56%
Aromatase binding - 0.5000 50.00%
PPAR gamma + 0.6068 60.68%
Honey bee toxicity - 0.8992 89.92%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.7900 79.00%
Fish aquatic toxicity + 0.9543 95.43%

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 94.19% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 90.85% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.50% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.70% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.61% 96.00%

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.
Gunnera perpensa

Cross-Links

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PubChem 11687109
LOTUS LTS0101114
wikiData Q105384801