2-Hydroxy-2-(2-hydroxyethyl)cyclohexan-1-one

Details

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Internal ID 1e6e2cbd-0fa8-4a71-b2db-e737f45bafa7
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Acyloins
IUPAC Name 2-hydroxy-2-(2-hydroxyethyl)cyclohexan-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H14O3/c9-6-5-8(11)4-2-1-3-7(8)10/h9,11H,1-6H2
InChI Key NFXUOWKJPHPQKG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C8H14O3
Molecular Weight 158.19 g/mol
Exact Mass 158.094294304 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 0.20
Atomic LogP (AlogP) 0.24
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Hydroxy-2-(2-hydroxyethyl)cyclohexan-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 + 0.9119 91.19%
Caco-2 + 0.6434 64.34%
Blood Brain Barrier - 0.6311 63.11%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.8994 89.94%
OATP2B1 inhibitior - 0.8427 84.27%
OATP1B1 inhibitior + 0.9276 92.76%
OATP1B3 inhibitior + 0.9524 95.24%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7292 72.92%
BSEP inhibitior - 0.9086 90.86%
P-glycoprotein inhibitior - 0.9882 98.82%
P-glycoprotein substrate - 0.9748 97.48%
CYP3A4 substrate - 0.6330 63.30%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7744 77.44%
CYP3A4 inhibition - 0.9527 95.27%
CYP2C9 inhibition - 0.7424 74.24%
CYP2C19 inhibition - 0.8550 85.50%
CYP2D6 inhibition - 0.9448 94.48%
CYP1A2 inhibition - 0.8998 89.98%
CYP2C8 inhibition - 0.9803 98.03%
CYP inhibitory promiscuity - 0.9729 97.29%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6962 69.62%
Eye corrosion - 0.9689 96.89%
Eye irritation + 0.9763 97.63%
Skin irritation - 0.6998 69.98%
Skin corrosion - 0.9512 95.12%
Ames mutagenesis - 0.7554 75.54%
Human Ether-a-go-go-Related Gene inhibition - 0.7833 78.33%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.6401 64.01%
skin sensitisation - 0.7901 79.01%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity - 0.5444 54.44%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.6770 67.70%
Acute Oral Toxicity (c) III 0.7106 71.06%
Estrogen receptor binding - 0.9656 96.56%
Androgen receptor binding - 0.7236 72.36%
Thyroid receptor binding - 0.8808 88.08%
Glucocorticoid receptor binding - 0.8051 80.51%
Aromatase binding - 0.8211 82.11%
PPAR gamma - 0.8232 82.32%
Honey bee toxicity - 0.9593 95.93%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.7400 74.00%
Fish aquatic toxicity - 0.7753 77.53%

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 92.72% 91.11%
CHEMBL2581 P07339 Cathepsin D 88.68% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.00% 94.45%
CHEMBL1937 Q92769 Histone deacetylase 2 86.13% 94.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.11% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.98% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.94% 96.09%

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.
Digitalis purpurea

Cross-Links

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PubChem 130038286
LOTUS LTS0031265
wikiData Q105178747