2-Acetyl-3-ethylpyrazine

Details

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Internal ID 44422d6e-eec5-4cbe-a9df-0e5434521532
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aryl ketones > Aryl alkyl ketones
IUPAC Name 1-(3-ethylpyrazin-2-yl)ethanone
SMILES (Canonical) CCC1=NC=CN=C1C(=O)C
SMILES (Isomeric) CCC1=NC=CN=C1C(=O)C
InChI InChI=1S/C8H10N2O/c1-3-7-8(6(2)11)10-5-4-9-7/h4-5H,3H2,1-2H3
InChI Key PPJSYGVFDJEMRP-UHFFFAOYSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C8H10N2O
Molecular Weight 150.18 g/mol
Exact Mass 150.079312947 g/mol
Topological Polar Surface Area (TPSA) 42.80 Ų
XlogP 0.60
Atomic LogP (AlogP) 1.24
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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32974-92-8
1-(3-ethylpyrazin-2-yl)ethanone
1-(3-Ethylpyrazinyl)ethan-1-one
Ethanone, 1-(3-ethylpyrazinyl)-
2-Acetyl-3-ethyl-1,4-diazine
2-acetyl-3-ethyl pyrazine
1-(3-ethylpyrazin-2-yl)ethan-1-one
1-(3-Ethylpyrazinyl)ethanone
FEMA No. 3250
3-Ethyl-2-acetylpyrazine
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2-Acetyl-3-ethylpyrazine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9957 99.57%
Caco-2 - 0.5721 57.21%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.8481 84.81%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9570 95.70%
OATP1B3 inhibitior + 0.9529 95.29%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7979 79.79%
P-glycoprotein inhibitior - 0.9896 98.96%
P-glycoprotein substrate - 0.8861 88.61%
CYP3A4 substrate - 0.7022 70.22%
CYP2C9 substrate + 0.6243 62.43%
CYP2D6 substrate - 0.8480 84.80%
CYP3A4 inhibition - 0.9539 95.39%
CYP2C9 inhibition - 0.9721 97.21%
CYP2C19 inhibition - 0.8741 87.41%
CYP2D6 inhibition - 0.9416 94.16%
CYP1A2 inhibition + 0.7206 72.06%
CYP2C8 inhibition - 0.9205 92.05%
CYP inhibitory promiscuity - 0.6843 68.43%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6900 69.00%
Carcinogenicity (trinary) Non-required 0.7109 71.09%
Eye corrosion - 0.9716 97.16%
Eye irritation + 0.7485 74.85%
Skin irritation - 0.5904 59.04%
Skin corrosion - 0.9032 90.32%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.5500 55.00%
Hepatotoxicity + 0.7500 75.00%
skin sensitisation - 0.6999 69.99%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity - 0.6144 61.44%
Acute Oral Toxicity (c) III 0.8531 85.31%
Estrogen receptor binding - 0.9699 96.99%
Androgen receptor binding - 0.8026 80.26%
Thyroid receptor binding - 0.7464 74.64%
Glucocorticoid receptor binding - 0.9469 94.69%
Aromatase binding - 0.8669 86.69%
PPAR gamma - 0.8827 88.27%
Honey bee toxicity - 0.9109 91.09%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.7400 74.00%
Fish aquatic toxicity - 0.9155 91.55%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.06% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.94% 85.14%
CHEMBL3401 O75469 Pregnane X receptor 85.92% 94.73%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.94% 97.25%
CHEMBL2581 P07339 Cathepsin D 83.70% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.36% 86.33%

Plants that contains it

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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.
Teucrium leucocladum

Cross-Links

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PubChem 61918
LOTUS LTS0089971
wikiData Q27274053