8-O-methylepiaustdiol

Details

Top
Internal ID 699569c1-c44b-4d0a-b45e-016b564d35d3
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones > Cyclohexenones
IUPAC Name (7S,8S)-7-hydroxy-8-methoxy-3,7-dimethyl-6-oxo-8H-isochromene-5-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H14O5/c1-7-4-8-9(5-14)11(15)13(2,16)12(17-3)10(8)6-18-7/h4-6,12,16H,1-3H3/t12-,13+/m0/s1
InChI Key CWVBDWQKTDGMNY-QWHCGFSZSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C13H14O5
Molecular Weight 250.25 g/mol
Exact Mass 250.08412354 g/mol
Topological Polar Surface Area (TPSA) 72.80 Ų
XlogP -0.60
Atomic LogP (AlogP) 0.65
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 8-O-methylepiaustdiol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9821 98.21%
Caco-2 + 0.6096 60.96%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7075 70.75%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7619 76.19%
OATP1B3 inhibitior + 0.9733 97.33%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8257 82.57%
P-glycoprotein inhibitior - 0.9013 90.13%
P-glycoprotein substrate - 0.9014 90.14%
CYP3A4 substrate + 0.5867 58.67%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8632 86.32%
CYP3A4 inhibition - 0.5706 57.06%
CYP2C9 inhibition - 0.9412 94.12%
CYP2C19 inhibition - 0.8331 83.31%
CYP2D6 inhibition - 0.9118 91.18%
CYP1A2 inhibition - 0.7354 73.54%
CYP2C8 inhibition - 0.7659 76.59%
CYP inhibitory promiscuity - 0.7102 71.02%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Danger 0.4508 45.08%
Eye corrosion - 0.9733 97.33%
Eye irritation - 0.5771 57.71%
Skin irritation - 0.5816 58.16%
Skin corrosion - 0.9536 95.36%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7701 77.01%
Micronuclear + 0.6200 62.00%
Hepatotoxicity + 0.6166 61.66%
skin sensitisation - 0.7642 76.42%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity + 0.6830 68.30%
Acute Oral Toxicity (c) III 0.4835 48.35%
Estrogen receptor binding + 0.5526 55.26%
Androgen receptor binding - 0.5731 57.31%
Thyroid receptor binding - 0.5994 59.94%
Glucocorticoid receptor binding - 0.8790 87.90%
Aromatase binding - 0.7293 72.93%
PPAR gamma + 0.5688 56.88%
Honey bee toxicity - 0.7638 76.38%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.7516 75.16%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.96% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 94.21% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.90% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.98% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.89% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.86% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.76% 96.09%
CHEMBL2581 P07339 Cathepsin D 85.05% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 84.06% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.91% 99.23%
CHEMBL340 P08684 Cytochrome P450 3A4 80.58% 91.19%

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 139587646
LOTUS LTS0010835
wikiData Q77571067