4,6-Dihydroxy-6-(2-hydroxyethyl)cyclohex-2-en-1-one

Details

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Internal ID a9948d28-1424-4a85-a698-f0697a863d1e
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones > Cyclohexenones
IUPAC Name 4,6-dihydroxy-6-(2-hydroxyethyl)cyclohex-2-en-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H12O4/c9-4-3-8(12)5-6(10)1-2-7(8)11/h1-2,6,9-10,12H,3-5H2
InChI Key ZNHAIJGMZCDGLQ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C8H12O4
Molecular Weight 172.18 g/mol
Exact Mass 172.07355886 g/mol
Topological Polar Surface Area (TPSA) 77.80 Ų
XlogP -0.70
Atomic LogP (AlogP) -1.01
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4,6-Dihydroxy-6-(2-hydroxyethyl)cyclohex-2-en-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8273 82.73%
Caco-2 - 0.6200 62.00%
Blood Brain Barrier - 0.5811 58.11%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.8567 85.67%
OATP2B1 inhibitior - 0.8523 85.23%
OATP1B1 inhibitior + 0.9501 95.01%
OATP1B3 inhibitior + 0.9536 95.36%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.6880 68.80%
BSEP inhibitior - 0.9329 93.29%
P-glycoprotein inhibitior - 0.9888 98.88%
P-glycoprotein substrate - 0.9059 90.59%
CYP3A4 substrate - 0.5356 53.56%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8587 85.87%
CYP3A4 inhibition - 0.8877 88.77%
CYP2C9 inhibition - 0.8348 83.48%
CYP2C19 inhibition - 0.8915 89.15%
CYP2D6 inhibition - 0.9316 93.16%
CYP1A2 inhibition - 0.8877 88.77%
CYP2C8 inhibition - 0.9686 96.86%
CYP inhibitory promiscuity - 0.9471 94.71%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9528 95.28%
Carcinogenicity (trinary) Non-required 0.7255 72.55%
Eye corrosion - 0.9785 97.85%
Eye irritation + 0.8628 86.28%
Skin irritation - 0.7067 70.67%
Skin corrosion - 0.9467 94.67%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8297 82.97%
Micronuclear - 0.8882 88.82%
Hepatotoxicity + 0.5067 50.67%
skin sensitisation - 0.7409 74.09%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity + 0.5357 53.57%
Acute Oral Toxicity (c) III 0.6683 66.83%
Estrogen receptor binding - 0.8985 89.85%
Androgen receptor binding - 0.7673 76.73%
Thyroid receptor binding - 0.7326 73.26%
Glucocorticoid receptor binding - 0.6679 66.79%
Aromatase binding - 0.9011 90.11%
PPAR gamma - 0.8144 81.44%
Honey bee toxicity - 0.9208 92.08%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity - 0.6615 66.15%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.28% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.81% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.91% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.95% 97.09%
CHEMBL226 P30542 Adenosine A1 receptor 85.53% 95.93%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.99% 95.56%
CHEMBL2581 P07339 Cathepsin D 84.61% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.28% 85.14%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.17% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.15% 94.45%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 81.27% 98.46%

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.
Bauhinia tarapotensis

Cross-Links

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PubChem 85408444
LOTUS LTS0169083
wikiData Q105380063