2-Isobutyl-3,5,6-trimethylpyrazine

Details

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Internal ID 7e01a226-91d3-4025-a882-d7e331d5bd07
Taxonomy Organoheterocyclic compounds > Diazines > Pyrazines
IUPAC Name 2,3,5-trimethyl-6-(2-methylpropyl)pyrazine
SMILES (Canonical) CC1=C(N=C(C(=N1)C)CC(C)C)C
SMILES (Isomeric) CC1=C(N=C(C(=N1)C)CC(C)C)C
InChI InChI=1S/C11H18N2/c1-7(2)6-11-10(5)12-8(3)9(4)13-11/h7H,6H2,1-5H3
InChI Key CMCOFWHSAGPVSF-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C11H18N2
Molecular Weight 178.27 g/mol
Exact Mass 178.146998583 g/mol
Topological Polar Surface Area (TPSA) 25.80 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.60
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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46187-37-5
2,3,5-trimethyl-6-(2-methylpropyl)pyrazine
trimethylisobutylpyrazine
2-(2-Methylpropyl)-3,5,6-trimethylpyrazine
Pyrazine, trimethyl(2-methylpropyl)-
Pyrazine, trimethyl(2-methylpropyl)- (9CI)
SCHEMBL10392933
DTXSID10334580
CMCOFWHSAGPVSF-UHFFFAOYSA-N
WBA18737
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-3,5,6-trimethylpyrazine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9954 99.54%
Caco-2 + 0.6932 69.32%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.8429 84.29%
Subcellular localzation Mitochondria 0.4932 49.32%
OATP2B1 inhibitior - 0.8601 86.01%
OATP1B1 inhibitior + 0.9552 95.52%
OATP1B3 inhibitior + 0.9442 94.42%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.7433 74.33%
P-glycoprotein inhibitior - 0.9680 96.80%
P-glycoprotein substrate - 0.9290 92.90%
CYP3A4 substrate - 0.7143 71.43%
CYP2C9 substrate - 0.8060 80.60%
CYP2D6 substrate - 0.7074 70.74%
CYP3A4 inhibition - 0.9387 93.87%
CYP2C9 inhibition - 0.9263 92.63%
CYP2C19 inhibition - 0.8656 86.56%
CYP2D6 inhibition - 0.8542 85.42%
CYP1A2 inhibition + 0.6195 61.95%
CYP2C8 inhibition - 0.9754 97.54%
CYP inhibitory promiscuity - 0.8906 89.06%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7500 75.00%
Carcinogenicity (trinary) Non-required 0.6237 62.37%
Eye corrosion - 0.9323 93.23%
Eye irritation + 0.8658 86.58%
Skin irritation + 0.5924 59.24%
Skin corrosion - 0.6545 65.45%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4523 45.23%
Micronuclear - 0.7000 70.00%
Hepatotoxicity + 0.7353 73.53%
skin sensitisation + 0.5363 53.63%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity + 0.5397 53.97%
Acute Oral Toxicity (c) III 0.5482 54.82%
Estrogen receptor binding - 0.9605 96.05%
Androgen receptor binding - 0.6983 69.83%
Thyroid receptor binding - 0.5552 55.52%
Glucocorticoid receptor binding - 0.8839 88.39%
Aromatase binding - 0.8076 80.76%
PPAR gamma - 0.8383 83.83%
Honey bee toxicity - 0.9658 96.58%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.6968 69.68%

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
CHEMBL2581 P07339 Cathepsin D 88.39% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 87.49% 89.63%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.64% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 83.95% 94.73%
CHEMBL2885 P07451 Carbonic anhydrase III 82.92% 87.45%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.60% 93.56%

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.
Crocus sativus
Lycium barbarum
Lycium chinense

Cross-Links

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PubChem 521191
NPASS NPC28815