5-(2-hydroxyethyl)-2,2,4,6-tetramethyl-3H-inden-1-one

Details

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Internal ID 75ea59a6-6e77-4b6f-8a34-bad9ec5fb055
Taxonomy Benzenoids > Indanes > Indanones
IUPAC Name 5-(2-hydroxyethyl)-2,2,4,6-tetramethyl-3H-inden-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H20O2/c1-9-7-12-13(8-15(3,4)14(12)17)10(2)11(9)5-6-16/h7,16H,5-6,8H2,1-4H3
InChI Key NUFTYHHRGFEVPH-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C15H20O2
Molecular Weight 232.32 g/mol
Exact Mass 232.146329876 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.60
H-Bond Acceptor 2
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 5-(2-hydroxyethyl)-2,2,4,6-tetramethyl-3H-inden-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 + 1.0000 100.00%
Caco-2 + 0.9540 95.40%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.6590 65.90%
OATP2B1 inhibitior - 0.8473 84.73%
OATP1B1 inhibitior + 0.8180 81.80%
OATP1B3 inhibitior + 0.9209 92.09%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.5314 53.14%
BSEP inhibitior - 0.8427 84.27%
P-glycoprotein inhibitior - 0.9305 93.05%
P-glycoprotein substrate - 0.8242 82.42%
CYP3A4 substrate - 0.5207 52.07%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7887 78.87%
CYP3A4 inhibition - 0.8555 85.55%
CYP2C9 inhibition - 0.8627 86.27%
CYP2C19 inhibition - 0.8920 89.20%
CYP2D6 inhibition - 0.9282 92.82%
CYP1A2 inhibition + 0.5639 56.39%
CYP2C8 inhibition - 0.8649 86.49%
CYP inhibitory promiscuity - 0.9347 93.47%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.6851 68.51%
Eye corrosion - 0.9786 97.86%
Eye irritation + 0.9396 93.96%
Skin irritation - 0.5485 54.85%
Skin corrosion - 0.9563 95.63%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6460 64.60%
Micronuclear - 0.9441 94.41%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation + 0.5428 54.28%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity + 0.5141 51.41%
Acute Oral Toxicity (c) III 0.7525 75.25%
Estrogen receptor binding - 0.7821 78.21%
Androgen receptor binding - 0.5558 55.58%
Thyroid receptor binding - 0.5766 57.66%
Glucocorticoid receptor binding - 0.6134 61.34%
Aromatase binding - 0.8322 83.22%
PPAR gamma - 0.5086 50.86%
Honey bee toxicity - 0.9397 93.97%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.8520 85.20%

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 94.01% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.52% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.16% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.56% 86.33%
CHEMBL4208 P20618 Proteasome component C5 85.54% 90.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.06% 89.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.70% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.44% 96.95%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 10728290
LOTUS LTS0117329
wikiData Q105185852