3,4-dihydroxy-6-(2-hydroxyethyl)-2,2,5,7-tetramethyl-3H-inden-1-one

Details

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Internal ID b1f8e41c-e5e7-493a-b18f-54443ca6f8f2
Taxonomy Benzenoids > Indanes > Indanones
IUPAC Name 3,4-dihydroxy-6-(2-hydroxyethyl)-2,2,5,7-tetramethyl-3H-inden-1-one
SMILES (Canonical) CC1=C(C(=C(C2=C1C(=O)C(C2O)(C)C)O)C)CCO
SMILES (Isomeric) CC1=C(C(=C(C2=C1C(=O)C(C2O)(C)C)O)C)CCO
InChI InChI=1S/C15H20O4/c1-7-9(5-6-16)8(2)12(17)11-10(7)13(18)15(3,4)14(11)19/h14,16-17,19H,5-6H2,1-4H3
InChI Key PRNYGOPDLNLLKK-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H20O4
Molecular Weight 264.32 g/mol
Exact Mass 264.13615911 g/mol
Topological Polar Surface Area (TPSA) 77.80 Ų
XlogP 1.40
Atomic LogP (AlogP) 1.80
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 3,4-dihydroxy-6-(2-hydroxyethyl)-2,2,5,7-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 + 0.9888 98.88%
Caco-2 + 0.7886 78.86%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.7019 70.19%
OATP2B1 inhibitior - 0.8537 85.37%
OATP1B1 inhibitior - 0.3247 32.47%
OATP1B3 inhibitior + 0.9368 93.68%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.9278 92.78%
P-glycoprotein inhibitior - 0.8893 88.93%
P-glycoprotein substrate - 0.8689 86.89%
CYP3A4 substrate + 0.5504 55.04%
CYP2C9 substrate - 0.7872 78.72%
CYP2D6 substrate - 0.7734 77.34%
CYP3A4 inhibition - 0.8142 81.42%
CYP2C9 inhibition - 0.7337 73.37%
CYP2C19 inhibition - 0.8112 81.12%
CYP2D6 inhibition - 0.9222 92.22%
CYP1A2 inhibition + 0.6715 67.15%
CYP2C8 inhibition - 0.7590 75.90%
CYP inhibitory promiscuity - 0.7557 75.57%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.6648 66.48%
Eye corrosion - 0.9886 98.86%
Eye irritation + 0.9230 92.30%
Skin irritation - 0.5847 58.47%
Skin corrosion - 0.9216 92.16%
Ames mutagenesis - 0.5928 59.28%
Human Ether-a-go-go-Related Gene inhibition - 0.4848 48.48%
Micronuclear - 0.8200 82.00%
Hepatotoxicity - 0.6307 63.07%
skin sensitisation - 0.7215 72.15%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity - 0.6010 60.10%
Acute Oral Toxicity (c) III 0.7115 71.15%
Estrogen receptor binding - 0.5672 56.72%
Androgen receptor binding - 0.6192 61.92%
Thyroid receptor binding + 0.5647 56.47%
Glucocorticoid receptor binding + 0.6591 65.91%
Aromatase binding - 0.7678 76.78%
PPAR gamma - 0.5895 58.95%
Honey bee toxicity - 0.9084 90.84%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7700 77.00%
Fish aquatic toxicity + 0.7932 79.32%

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 94.31% 91.11%
CHEMBL2581 P07339 Cathepsin D 92.46% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.08% 95.56%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 86.50% 86.92%
CHEMBL1937 Q92769 Histone deacetylase 2 86.27% 94.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.45% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.23% 94.45%
CHEMBL240 Q12809 HERG 80.18% 89.76%

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 162944737
LOTUS LTS0149734
wikiData Q104195300