2-Isobutyl-3-methylpyrazine

Details

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Internal ID 62eec08c-0df6-4ef9-8750-d046d923d583
Taxonomy Organoheterocyclic compounds > Diazines > Pyrazines
IUPAC Name 2-methyl-3-(2-methylpropyl)pyrazine
SMILES (Canonical) CC1=NC=CN=C1CC(C)C
SMILES (Isomeric) CC1=NC=CN=C1CC(C)C
InChI InChI=1S/C9H14N2/c1-7(2)6-9-8(3)10-4-5-11-9/h4-5,7H,6H2,1-3H3
InChI Key ZHMIODDNZRIENW-UHFFFAOYSA-N
Popularity 21 references in papers

Physical and Chemical Properties

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Molecular Formula C9H14N2
Molecular Weight 150.22 g/mol
Exact Mass 150.115698455 g/mol
Topological Polar Surface Area (TPSA) 25.80 Ų
XlogP 2.00
Atomic LogP (AlogP) 1.98
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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13925-06-9
2-Methyl-3-(2-methylpropyl)pyrazine
2-isobutyl-3-methyl pyrazine
2-Methyl-3-isobutylpyrazine
Pyrazine, 2-methyl-3-(2-methylpropyl)-
FEMA No. 3133
UNII-11EP4V0M9Z
3-Methyl-2-isobutyl pyrazine
11EP4V0M9Z
Pyrazine, 2-isobutyl-3-methyl-
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-Isobutyl-3-methylpyrazine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9959 99.59%
Caco-2 - 0.6552 65.52%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.7857 78.57%
Subcellular localzation Mitochondria 0.5859 58.59%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9516 95.16%
OATP1B3 inhibitior + 0.9481 94.81%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.7629 76.29%
P-glycoprotein inhibitior - 0.9864 98.64%
P-glycoprotein substrate - 0.8852 88.52%
CYP3A4 substrate - 0.7283 72.83%
CYP2C9 substrate - 0.8060 80.60%
CYP2D6 substrate - 0.7074 70.74%
CYP3A4 inhibition - 0.9069 90.69%
CYP2C9 inhibition - 0.9314 93.14%
CYP2C19 inhibition - 0.8616 86.16%
CYP2D6 inhibition - 0.8408 84.08%
CYP1A2 inhibition + 0.6497 64.97%
CYP2C8 inhibition - 0.9607 96.07%
CYP inhibitory promiscuity - 0.8825 88.25%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7400 74.00%
Carcinogenicity (trinary) Non-required 0.6382 63.82%
Eye corrosion - 0.9307 93.07%
Eye irritation + 0.9316 93.16%
Skin irritation + 0.6292 62.92%
Skin corrosion - 0.6458 64.58%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4678 46.78%
Micronuclear - 0.6400 64.00%
Hepatotoxicity + 0.7353 73.53%
skin sensitisation + 0.5267 52.67%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.7161 71.61%
Acute Oral Toxicity (c) III 0.5167 51.67%
Estrogen receptor binding - 0.9796 97.96%
Androgen receptor binding - 0.7998 79.98%
Thyroid receptor binding - 0.8566 85.66%
Glucocorticoid receptor binding - 0.9494 94.94%
Aromatase binding - 0.8709 87.09%
PPAR gamma - 0.9538 95.38%
Honey bee toxicity - 0.9537 95.37%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.6578 65.78%

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
CHEMBL3401 O75469 Pregnane X receptor 91.74% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.55% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.87% 98.95%
CHEMBL3492 P49721 Proteasome Macropain subunit 86.13% 90.24%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 83.89% 93.10%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.47% 96.00%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 80.87% 93.65%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.83% 100.00%

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.
Perilla frutescens

Cross-Links

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PubChem 26333
NPASS NPC109452
LOTUS LTS0094695
wikiData Q27251319