2,3,5-Trimethyl-6-propylpyrazine

Details

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Internal ID a3107a6f-05dd-4aa0-a550-ef6b423190f1
Taxonomy Organoheterocyclic compounds > Diazines > Pyrazines
IUPAC Name 2,3,5-trimethyl-6-propylpyrazine
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H16N2/c1-5-6-10-9(4)11-7(2)8(3)12-10/h5-6H2,1-4H3
InChI Key GEPYSCIASYXPCY-UHFFFAOYSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16N2
Molecular Weight 164.25 g/mol
Exact Mass 164.131348519 g/mol
Topological Polar Surface Area (TPSA) 25.80 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.35
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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trimethylpropylpyrazine
92233-82-4
2-propyl-3,5,6-trimethylpyrazine
Pyrazine, trimethylpropyl
T9BZ8DX9HK
2,3,5-trimethyl-6-propyl-pyrazine
UNII-T9BZ8DX9HK
Pyrazine, 2,3,5-trimethyl-6-propyl-
Pyrazine, trimethylpropyl-
SCHEMBL7154330
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2,3,5-Trimethyl-6-propylpyrazine

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 + 0.8633 86.33%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.8286 82.86%
Subcellular localzation Mitochondria 0.3574 35.74%
OATP2B1 inhibitior - 0.8514 85.14%
OATP1B1 inhibitior + 0.9474 94.74%
OATP1B3 inhibitior + 0.9433 94.33%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior - 0.7859 78.59%
P-glycoprotein inhibitior - 0.9729 97.29%
P-glycoprotein substrate - 0.8817 88.17%
CYP3A4 substrate - 0.6856 68.56%
CYP2C9 substrate - 0.6057 60.57%
CYP2D6 substrate - 0.7086 70.86%
CYP3A4 inhibition - 0.9791 97.91%
CYP2C9 inhibition - 0.8869 88.69%
CYP2C19 inhibition - 0.8201 82.01%
CYP2D6 inhibition - 0.8426 84.26%
CYP1A2 inhibition + 0.7037 70.37%
CYP2C8 inhibition - 0.9017 90.17%
CYP inhibitory promiscuity - 0.7961 79.61%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8300 83.00%
Carcinogenicity (trinary) Non-required 0.6114 61.14%
Eye corrosion - 0.9322 93.22%
Eye irritation + 0.7975 79.75%
Skin irritation + 0.5726 57.26%
Skin corrosion - 0.7014 70.14%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5223 52.23%
Micronuclear - 0.8000 80.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation + 0.4890 48.90%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity + 0.5137 51.37%
Acute Oral Toxicity (c) II 0.6355 63.55%
Estrogen receptor binding - 0.8968 89.68%
Androgen receptor binding - 0.7348 73.48%
Thyroid receptor binding - 0.5599 55.99%
Glucocorticoid receptor binding - 0.8694 86.94%
Aromatase binding - 0.8390 83.90%
PPAR gamma - 0.8342 83.42%
Honey bee toxicity - 0.9803 98.03%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity - 0.3976 39.76%

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
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 85.40% 93.65%
CHEMBL2581 P07339 Cathepsin D 84.82% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.95% 96.09%
CHEMBL1907 P15144 Aminopeptidase N 81.99% 93.31%
CHEMBL3401 O75469 Pregnane X receptor 81.96% 94.73%
CHEMBL230 P35354 Cyclooxygenase-2 81.02% 89.63%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.07% 86.33%

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 586005
LOTUS LTS0211238
wikiData Q82113957