(8S)-8-ethyl-3-(hydroxymethyl)-2,8-dimethylchromene-4,7-dione

Details

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Internal ID 752397f0-8505-406d-b82b-a16e5b3529d3
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name (8S)-8-ethyl-3-(hydroxymethyl)-2,8-dimethylchromene-4,7-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H16O4/c1-4-14(3)11(16)6-5-9-12(17)10(7-15)8(2)18-13(9)14/h5-6,15H,4,7H2,1-3H3/t14-/m1/s1
InChI Key JUWRYWAZYBSNCI-CQSZACIVSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C14H16O4
Molecular Weight 248.27 g/mol
Exact Mass 248.10485899 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 1.40
Atomic LogP (AlogP) 1.70
H-Bond Acceptor 4
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 (8S)-8-ethyl-3-(hydroxymethyl)-2,8-dimethylchromene-4,7-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9933 99.33%
Caco-2 + 0.8829 88.29%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.6270 62.70%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8246 82.46%
OATP1B3 inhibitior + 0.9560 95.60%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.6053 60.53%
P-glycoprotein inhibitior - 0.9350 93.50%
P-glycoprotein substrate - 0.8712 87.12%
CYP3A4 substrate - 0.5355 53.55%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8683 86.83%
CYP3A4 inhibition - 0.5735 57.35%
CYP2C9 inhibition - 0.5856 58.56%
CYP2C19 inhibition - 0.5204 52.04%
CYP2D6 inhibition - 0.9318 93.18%
CYP1A2 inhibition + 0.7897 78.97%
CYP2C8 inhibition - 0.9124 91.24%
CYP inhibitory promiscuity - 0.5302 53.02%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9013 90.13%
Carcinogenicity (trinary) Non-required 0.6737 67.37%
Eye corrosion - 0.9853 98.53%
Eye irritation + 0.5791 57.91%
Skin irritation - 0.7183 71.83%
Skin corrosion - 0.9403 94.03%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7804 78.04%
Micronuclear - 0.6341 63.41%
Hepatotoxicity + 0.5561 55.61%
skin sensitisation - 0.7469 74.69%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity + 0.5448 54.48%
Acute Oral Toxicity (c) III 0.4816 48.16%
Estrogen receptor binding + 0.5641 56.41%
Androgen receptor binding + 0.6478 64.78%
Thyroid receptor binding - 0.6483 64.83%
Glucocorticoid receptor binding - 0.5066 50.66%
Aromatase binding - 0.4938 49.38%
PPAR gamma + 0.5500 55.00%
Honey bee toxicity - 0.9671 96.71%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.9835 98.35%

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
CHEMBL3192 Q9BY41 Histone deacetylase 8 93.21% 93.99%
CHEMBL2581 P07339 Cathepsin D 92.90% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 92.49% 94.73%
CHEMBL230 P35354 Cyclooxygenase-2 92.01% 89.63%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.99% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.06% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.12% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.12% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.02% 94.00%

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 92469091
LOTUS LTS0063112
wikiData Q105135482