2,5-Dimethylpyrazine

Details

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Internal ID 55675e66-1a49-4998-92ce-b303b69c21fc
Taxonomy Organoheterocyclic compounds > Diazines > Pyrazines
IUPAC Name 2,5-dimethylpyrazine
SMILES (Canonical) CC1=CN=C(C=N1)C
SMILES (Isomeric) CC1=CN=C(C=N1)C
InChI InChI=1S/C6H8N2/c1-5-3-8-6(2)4-7-5/h3-4H,1-2H3
InChI Key LCZUOKDVTBMCMX-UHFFFAOYSA-N
Popularity 555 references in papers

Physical and Chemical Properties

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Molecular Formula C6H8N2
Molecular Weight 108.14 g/mol
Exact Mass 108.068748264 g/mol
Topological Polar Surface Area (TPSA) 25.80 Ų
XlogP 0.60
Atomic LogP (AlogP) 1.09
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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123-32-0
2,5-Dimethyl pyrazine
Pyrazine, 2,5-dimethyl-
2,5-Dimethyl-1,4-diazine
2,5-Dimethylpiazine
2,5-Dimethylparadiazine
NSC 49139
FEMA No. 3272
2,5-Dimethyl-pyrazine
CCRIS 2929
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2,5-Dimethylpyrazine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9922 99.22%
Caco-2 + 0.5671 56.71%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.9286 92.86%
Subcellular localzation Mitochondria 0.6577 65.77%
OATP2B1 inhibitior - 0.8756 87.56%
OATP1B1 inhibitior + 0.9803 98.03%
OATP1B3 inhibitior + 0.9607 96.07%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7967 79.67%
P-glycoprotein inhibitior - 0.9825 98.25%
P-glycoprotein substrate - 0.9851 98.51%
CYP3A4 substrate - 0.7805 78.05%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.7923 79.23%
CYP3A4 inhibition - 0.8951 89.51%
CYP2C9 inhibition - 0.9835 98.35%
CYP2C19 inhibition - 0.9412 94.12%
CYP2D6 inhibition - 0.9329 93.29%
CYP1A2 inhibition - 0.6575 65.75%
CYP2C8 inhibition - 0.9863 98.63%
CYP inhibitory promiscuity - 0.9356 93.56%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7900 79.00%
Carcinogenicity (trinary) Non-required 0.5991 59.91%
Eye corrosion + 0.8446 84.46%
Eye irritation + 0.9948 99.48%
Skin irritation + 0.8923 89.23%
Skin corrosion + 0.6160 61.60%
Ames mutagenesis - 0.9700 97.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6864 68.64%
Micronuclear - 0.5500 55.00%
Hepatotoxicity + 0.8427 84.27%
skin sensitisation + 0.5428 54.28%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity + 0.4627 46.27%
Acute Oral Toxicity (c) III 0.8125 81.25%
Estrogen receptor binding - 0.9549 95.49%
Androgen receptor binding - 0.9490 94.90%
Thyroid receptor binding - 0.8455 84.55%
Glucocorticoid receptor binding - 0.9391 93.91%
Aromatase binding - 0.8809 88.09%
PPAR gamma - 0.8877 88.77%
Honey bee toxicity - 0.9775 97.75%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.7300 73.00%
Fish aquatic toxicity - 0.8906 89.06%

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 85.81% 93.65%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 82.19% 93.10%
CHEMBL3401 O75469 Pregnane X receptor 81.29% 94.73%

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
Phlomoides umbrosa
Platycladus orientalis

Cross-Links

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PubChem 31252
NPASS NPC204104
LOTUS LTS0198805
wikiData Q27161950