5-Isobutyl-3-methoxy-2-methylpyrazine

Details

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Internal ID dc2d6394-25c9-49ca-9f4f-3e83da5472dc
Taxonomy Organoheterocyclic compounds > Diazines > Pyrazines > Methoxypyrazines
IUPAC Name 3-methoxy-2-methyl-5-(2-methylpropyl)pyrazine
SMILES (Canonical) CC1=NC=C(N=C1OC)CC(C)C
SMILES (Isomeric) CC1=NC=C(N=C1OC)CC(C)C
InChI InChI=1S/C10H16N2O/c1-7(2)5-9-6-11-8(3)10(12-9)13-4/h6-7H,5H2,1-4H3
InChI Key JFWOXJAVBQVXGU-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C10H16N2O
Molecular Weight 180.25 g/mol
Exact Mass 180.126263138 g/mol
Topological Polar Surface Area (TPSA) 35.00 Ų
XlogP 2.10
Atomic LogP (AlogP) 1.99
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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RefChem:102979
3-methoxy-2-methyl-5-(2-methylpropyl)pyrazine
SCHEMBL16432838
CHEBI:214128

2D Structure

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2D Structure of 5-Isobutyl-3-methoxy-2-methylpyrazine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9930 99.30%
Caco-2 + 0.6361 63.61%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.7908 79.08%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9294 92.94%
OATP1B3 inhibitior + 0.9507 95.07%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8845 88.45%
P-glycoprotein inhibitior - 0.9758 97.58%
P-glycoprotein substrate - 0.8832 88.32%
CYP3A4 substrate - 0.6128 61.28%
CYP2C9 substrate - 0.8120 81.20%
CYP2D6 substrate - 0.6801 68.01%
CYP3A4 inhibition - 0.9292 92.92%
CYP2C9 inhibition - 0.9613 96.13%
CYP2C19 inhibition - 0.7011 70.11%
CYP2D6 inhibition - 0.9328 93.28%
CYP1A2 inhibition + 0.5723 57.23%
CYP2C8 inhibition - 0.8900 89.00%
CYP inhibitory promiscuity - 0.7823 78.23%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8300 83.00%
Carcinogenicity (trinary) Non-required 0.6720 67.20%
Eye corrosion - 0.9678 96.78%
Eye irritation + 0.9240 92.40%
Skin irritation - 0.7490 74.90%
Skin corrosion - 0.8893 88.93%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3642 36.42%
Micronuclear - 0.5700 57.00%
Hepatotoxicity + 0.6931 69.31%
skin sensitisation - 0.8027 80.27%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.7458 74.58%
Acute Oral Toxicity (c) III 0.6149 61.49%
Estrogen receptor binding - 0.9623 96.23%
Androgen receptor binding - 0.9132 91.32%
Thyroid receptor binding - 0.7457 74.57%
Glucocorticoid receptor binding - 0.9128 91.28%
Aromatase binding - 0.7467 74.67%
PPAR gamma - 0.9279 92.79%
Honey bee toxicity - 0.9483 94.83%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity - 0.7793 77.93%

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 93.57% 96.09%
CHEMBL2885 P07451 Carbonic anhydrase III 88.65% 87.45%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 88.23% 92.68%
CHEMBL1907 P15144 Aminopeptidase N 88.04% 93.31%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.63% 96.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.52% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 84.99% 94.73%
CHEMBL1937 Q92769 Histone deacetylase 2 84.69% 94.75%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 84.65% 93.10%
CHEMBL3492 P49721 Proteasome Macropain subunit 84.44% 90.24%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 82.87% 93.65%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.82% 99.17%
CHEMBL235 P37231 Peroxisome proliferator-activated receptor gamma 81.07% 95.39%
CHEMBL2581 P07339 Cathepsin D 80.85% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 80.56% 89.63%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 80.31% 96.67%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 11679914
LOTUS LTS0047241
wikiData Q77561033