(3Z)-3-(1-aminoethylidene)-6-methylpyran-2,4-dione

Details

Top
Internal ID 63ed07ef-fcfb-4bfb-929e-205787312497
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives > Dihydropyranones
IUPAC Name (3Z)-3-(1-aminoethylidene)-6-methylpyran-2,4-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H9NO3/c1-4-3-6(10)7(5(2)9)8(11)12-4/h3H,9H2,1-2H3/b7-5-
InChI Key ONMOQSQBAAMLAG-ALCCZGGFSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C8H9NO3
Molecular Weight 167.16 g/mol
Exact Mass 167.058243149 g/mol
Topological Polar Surface Area (TPSA) 69.40 Ų
XlogP 0.80
Atomic LogP (AlogP) 0.25
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (3Z)-3-(1-aminoethylidene)-6-methylpyran-2,4-dione

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9897 98.97%
Caco-2 + 0.6017 60.17%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.4767 47.67%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9464 94.64%
OATP1B3 inhibitior + 0.9679 96.79%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9241 92.41%
P-glycoprotein inhibitior - 0.9775 97.75%
P-glycoprotein substrate - 0.9617 96.17%
CYP3A4 substrate - 0.6639 66.39%
CYP2C9 substrate - 0.8005 80.05%
CYP2D6 substrate - 0.8741 87.41%
CYP3A4 inhibition - 0.9058 90.58%
CYP2C9 inhibition - 0.9329 93.29%
CYP2C19 inhibition - 0.8090 80.90%
CYP2D6 inhibition - 0.9302 93.02%
CYP1A2 inhibition - 0.7915 79.15%
CYP2C8 inhibition - 0.9735 97.35%
CYP inhibitory promiscuity - 0.8887 88.87%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Non-required 0.4865 48.65%
Eye corrosion - 0.9442 94.42%
Eye irritation + 0.9447 94.47%
Skin irritation - 0.6113 61.13%
Skin corrosion - 0.9085 90.85%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7680 76.80%
Micronuclear + 0.7700 77.00%
Hepatotoxicity + 0.7783 77.83%
skin sensitisation - 0.8418 84.18%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity + 0.4887 48.87%
Acute Oral Toxicity (c) III 0.5712 57.12%
Estrogen receptor binding - 0.8903 89.03%
Androgen receptor binding - 0.5937 59.37%
Thyroid receptor binding - 0.8644 86.44%
Glucocorticoid receptor binding - 0.7842 78.42%
Aromatase binding - 0.7675 76.75%
PPAR gamma - 0.8599 85.99%
Honey bee toxicity - 0.9596 95.96%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity - 0.5193 51.93%

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 92.08% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.37% 91.11%
CHEMBL2581 P07339 Cathepsin D 88.72% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 86.30% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.22% 99.23%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 84.16% 93.65%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.38% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.85% 85.14%

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 5710126
LOTUS LTS0271554
wikiData Q103784991