4-Hydroxy-4-(2-hydroxypropan-2-yl)cyclohex-2-en-1-one

Details

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Internal ID b59d4eaa-417b-4a01-8272-04aa1b12c301
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones > Cyclohexenones
IUPAC Name 4-hydroxy-4-(2-hydroxypropan-2-yl)cyclohex-2-en-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H14O3/c1-8(2,11)9(12)5-3-7(10)4-6-9/h3,5,11-12H,4,6H2,1-2H3
InChI Key PPUIVANKQVBONX-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C9H14O3
Molecular Weight 170.21 g/mol
Exact Mass 170.094294304 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP -0.50
Atomic LogP (AlogP) 0.41
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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903570-27-4
EN300-7504623

2D Structure

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2D Structure of 4-Hydroxy-4-(2-hydroxypropan-2-yl)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 + 0.9866 98.66%
Caco-2 + 0.8876 88.76%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.8636 86.36%
OATP2B1 inhibitior - 0.8579 85.79%
OATP1B1 inhibitior + 0.9602 96.02%
OATP1B3 inhibitior + 0.9710 97.10%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9239 92.39%
P-glycoprotein inhibitior - 0.9858 98.58%
P-glycoprotein substrate - 0.9646 96.46%
CYP3A4 substrate - 0.5495 54.95%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8582 85.82%
CYP3A4 inhibition - 0.8984 89.84%
CYP2C9 inhibition - 0.8559 85.59%
CYP2C19 inhibition - 0.9145 91.45%
CYP2D6 inhibition - 0.9302 93.02%
CYP1A2 inhibition - 0.8864 88.64%
CYP2C8 inhibition - 0.9831 98.31%
CYP inhibitory promiscuity - 0.9687 96.87%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.6341 63.41%
Eye corrosion - 0.9230 92.30%
Eye irritation + 0.8436 84.36%
Skin irritation + 0.5932 59.32%
Skin corrosion - 0.7569 75.69%
Ames mutagenesis - 0.8270 82.70%
Human Ether-a-go-go-Related Gene inhibition - 0.7920 79.20%
Micronuclear - 0.8600 86.00%
Hepatotoxicity + 0.5658 56.58%
skin sensitisation + 0.6750 67.50%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity - 0.5562 55.62%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.6143 61.43%
Acute Oral Toxicity (c) III 0.7859 78.59%
Estrogen receptor binding - 0.7409 74.09%
Androgen receptor binding - 0.8285 82.85%
Thyroid receptor binding - 0.8686 86.86%
Glucocorticoid receptor binding - 0.6883 68.83%
Aromatase binding - 0.8665 86.65%
PPAR gamma - 0.8985 89.85%
Honey bee toxicity - 0.9721 97.21%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity - 0.4025 40.25%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.87% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.50% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.54% 95.56%
CHEMBL2581 P07339 Cathepsin D 89.12% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.35% 96.09%
CHEMBL4208 P20618 Proteasome component C5 82.05% 90.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.39% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.29% 85.14%

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.
Hydrocotyle leucocephala

Cross-Links

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PubChem 11600745
LOTUS LTS0257503
wikiData Q105213047