8-Ethyl-5,7-dihydroxy-2-methyl-4-chromanone

Details

Top
Internal ID 4f3d42b9-2479-4916-b685-4d705ada6ab4
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Chromones
IUPAC Name 8-ethyl-5,7-dihydroxy-2-methyl-2,3-dihydrochromen-4-one
SMILES (Canonical) CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C
SMILES (Isomeric) CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C
InChI InChI=1S/C12H14O4/c1-3-7-8(13)5-10(15)11-9(14)4-6(2)16-12(7)11/h5-6,13,15H,3-4H2,1-2H3
InChI Key RJLGVWYEZQYNKN-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C12H14O4
Molecular Weight 222.24 g/mol
Exact Mass 222.08920892 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.01
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

Top
8-ethyl-5,7-dihydroxy-2-methyl-4-chromanone

2D Structure

Top
2D Structure of 8-Ethyl-5,7-dihydroxy-2-methyl-4-chromanone

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9407 94.07%
Caco-2 + 0.8509 85.09%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.6707 67.07%
OATP2B1 inhibitior - 0.8561 85.61%
OATP1B1 inhibitior + 0.8762 87.62%
OATP1B3 inhibitior + 0.9618 96.18%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9223 92.23%
P-glycoprotein inhibitior - 0.9375 93.75%
P-glycoprotein substrate - 0.8821 88.21%
CYP3A4 substrate - 0.5983 59.83%
CYP2C9 substrate - 0.7974 79.74%
CYP2D6 substrate - 0.7747 77.47%
CYP3A4 inhibition + 0.6124 61.24%
CYP2C9 inhibition + 0.5653 56.53%
CYP2C19 inhibition + 0.6397 63.97%
CYP2D6 inhibition - 0.7722 77.22%
CYP1A2 inhibition + 0.8112 81.12%
CYP2C8 inhibition - 0.9080 90.80%
CYP inhibitory promiscuity + 0.6183 61.83%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6653 66.53%
Eye corrosion - 0.9837 98.37%
Eye irritation + 0.9668 96.68%
Skin irritation - 0.7014 70.14%
Skin corrosion - 0.8916 89.16%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5134 51.34%
Micronuclear + 0.5859 58.59%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation - 0.7298 72.98%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity - 0.6949 69.49%
Acute Oral Toxicity (c) III 0.3019 30.19%
Estrogen receptor binding + 0.6778 67.78%
Androgen receptor binding + 0.7099 70.99%
Thyroid receptor binding - 0.5290 52.90%
Glucocorticoid receptor binding + 0.6268 62.68%
Aromatase binding - 0.9113 91.13%
PPAR gamma - 0.6012 60.12%
Honey bee toxicity - 0.9447 94.47%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9062 90.62%

Targets

Top

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 96.54% 91.11%
CHEMBL2581 P07339 Cathepsin D 94.71% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.84% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.05% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.57% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 86.52% 94.73%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 86.08% 94.80%
CHEMBL2964 P36507 Dual specificity mitogen-activated protein kinase kinase 2 85.93% 80.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.77% 86.33%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.93% 90.71%

Plants that contains it

Top
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.
There are no matching plants.

Cross-Links

Top
PubChem 74202867
LOTUS LTS0195871
wikiData Q77503725