4-Hydroxy-4-(2-hydroxyethyl)cyclohex-2-en-1-one

Details

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Internal ID 4b1a8a73-221e-433e-8ab2-787230005a25
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones > Cyclohexenones
IUPAC Name 4-hydroxy-4-(2-hydroxyethyl)cyclohex-2-en-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H12O3/c9-6-5-8(11)3-1-7(10)2-4-8/h1,3,9,11H,2,4-6H2
InChI Key JGWLQWUVJUFKHJ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C8H12O3
Molecular Weight 156.18 g/mol
Exact Mass 156.078644241 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP -0.20
Atomic LogP (AlogP) 0.02
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 4-Hydroxy-4-(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 + 0.9628 96.28%
Caco-2 + 0.7981 79.81%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.8773 87.73%
OATP2B1 inhibitior - 0.8554 85.54%
OATP1B1 inhibitior + 0.9297 92.97%
OATP1B3 inhibitior + 0.9534 95.34%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7130 71.30%
BSEP inhibitior - 0.8770 87.70%
P-glycoprotein inhibitior - 0.9828 98.28%
P-glycoprotein substrate - 0.9640 96.40%
CYP3A4 substrate - 0.5998 59.98%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8406 84.06%
CYP3A4 inhibition - 0.8781 87.81%
CYP2C9 inhibition - 0.7416 74.16%
CYP2C19 inhibition - 0.7276 72.76%
CYP2D6 inhibition - 0.9194 91.94%
CYP1A2 inhibition - 0.8894 88.94%
CYP2C8 inhibition - 0.9756 97.56%
CYP inhibitory promiscuity - 0.9367 93.67%
UGT catelyzed + 0.6362 63.62%
Carcinogenicity (binary) - 0.9428 94.28%
Carcinogenicity (trinary) Non-required 0.6729 67.29%
Eye corrosion - 0.9500 95.00%
Eye irritation + 0.9797 97.97%
Skin irritation - 0.7403 74.03%
Skin corrosion - 0.9733 97.33%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8446 84.46%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.5802 58.02%
skin sensitisation - 0.7680 76.80%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity - 0.5778 57.78%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.5872 58.72%
Acute Oral Toxicity (c) III 0.7883 78.83%
Estrogen receptor binding - 0.8922 89.22%
Androgen receptor binding - 0.7900 79.00%
Thyroid receptor binding - 0.8843 88.43%
Glucocorticoid receptor binding - 0.7408 74.08%
Aromatase binding - 0.8547 85.47%
PPAR gamma - 0.7013 70.13%
Honey bee toxicity - 0.9678 96.78%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity - 0.6407 64.07%

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 96.71% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.76% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.57% 95.56%
CHEMBL4208 P20618 Proteasome component C5 83.73% 90.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.70% 96.09%
CHEMBL2581 P07339 Cathepsin D 81.35% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.60% 100.00%

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.
Teucrium decipiens

Cross-Links

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PubChem 163192686
LOTUS LTS0011162
wikiData Q105127743