(e)-2,5-Dimethyl-3-styrylpyrazine

Details

Top
Internal ID 3e89c8bc-5ea5-4b1b-add8-7d616484ad57
Taxonomy Benzenoids > Benzene and substituted derivatives > Styrenes
IUPAC Name 2,5-dimethyl-3-[(E)-2-phenylethenyl]pyrazine
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H14N2/c1-11-10-15-12(2)14(16-11)9-8-13-6-4-3-5-7-13/h3-10H,1-2H3/b9-8+
InChI Key FVNPLROTBAEWRZ-CMDGGOBGSA-N
Popularity 6 references in papers

Physical and Chemical Properties

Top
Molecular Formula C14H14N2
Molecular Weight 210.27 g/mol
Exact Mass 210.115698455 g/mol
Topological Polar Surface Area (TPSA) 25.80 Ų
XlogP 2.90
Atomic LogP (AlogP) 3.26
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (e)-2,5-Dimethyl-3-styrylpyrazine

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9945 99.45%
Caco-2 + 0.7551 75.51%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.5715 57.15%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9564 95.64%
OATP1B3 inhibitior + 0.9591 95.91%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.7728 77.28%
P-glycoprotein inhibitior - 0.9286 92.86%
P-glycoprotein substrate - 0.9435 94.35%
CYP3A4 substrate - 0.6358 63.58%
CYP2C9 substrate + 0.6107 61.07%
CYP2D6 substrate - 0.8011 80.11%
CYP3A4 inhibition - 0.6774 67.74%
CYP2C9 inhibition - 0.7132 71.32%
CYP2C19 inhibition + 0.5968 59.68%
CYP2D6 inhibition - 0.7476 74.76%
CYP1A2 inhibition + 0.8472 84.72%
CYP2C8 inhibition + 0.4844 48.44%
CYP inhibitory promiscuity + 0.7433 74.33%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8000 80.00%
Carcinogenicity (trinary) Non-required 0.6096 60.96%
Eye corrosion - 0.9540 95.40%
Eye irritation + 0.9135 91.35%
Skin irritation + 0.6507 65.07%
Skin corrosion - 0.9198 91.98%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7675 76.75%
Micronuclear - 0.5000 50.00%
Hepatotoxicity + 0.5927 59.27%
skin sensitisation + 0.5202 52.02%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.6625 66.25%
Acute Oral Toxicity (c) III 0.8787 87.87%
Estrogen receptor binding + 0.8935 89.35%
Androgen receptor binding - 0.5531 55.31%
Thyroid receptor binding - 0.6003 60.03%
Glucocorticoid receptor binding - 0.6467 64.67%
Aromatase binding + 0.7788 77.88%
PPAR gamma - 0.5935 59.35%
Honey bee toxicity - 0.9659 96.59%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.8400 84.00%
Fish aquatic toxicity + 0.8137 81.37%

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
CHEMBL3192 Q9BY41 Histone deacetylase 8 94.38% 93.99%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 93.67% 96.00%
CHEMBL2039 P27338 Monoamine oxidase B 92.99% 92.51%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.24% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.23% 86.33%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 91.36% 94.62%
CHEMBL1937 Q92769 Histone deacetylase 2 89.84% 94.75%
CHEMBL1951 P21397 Monoamine oxidase A 88.72% 91.49%
CHEMBL3401 O75469 Pregnane X receptor 87.45% 94.73%
CHEMBL5805 Q9NR97 Toll-like receptor 8 84.88% 96.25%
CHEMBL2243 O00519 Anandamide amidohydrolase 84.04% 97.53%
CHEMBL1907599 P05556 Integrin alpha-4/beta-1 83.67% 92.86%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 80.27% 85.49%

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 13614455
LOTUS LTS0211608
wikiData Q105002581