2,4-Dimethylimidazole

Details

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Internal ID fc084905-a619-4036-afeb-e91aaf9af594
Taxonomy Organoheterocyclic compounds > Azoles > Imidazoles
IUPAC Name 2,5-dimethyl-1H-imidazole
SMILES (Canonical) CC1=CN=C(N1)C
SMILES (Isomeric) CC1=CN=C(N1)C
InChI InChI=1S/C5H8N2/c1-4-3-6-5(2)7-4/h3H,1-2H3,(H,6,7)
InChI Key LLPKQRMDOFYSGZ-UHFFFAOYSA-N
Popularity 36 references in papers

Physical and Chemical Properties

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Molecular Formula C5H8N2
Molecular Weight 96.13 g/mol
Exact Mass 96.068748264 g/mol
Topological Polar Surface Area (TPSA) 28.70 Ų
XlogP 0.90
Atomic LogP (AlogP) 1.03
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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930-62-1
2,4-Dimethyl-1H-imidazole
1H-Imidazole, 2,4-dimethyl-
2,5-dimethyl-1H-imidazole
EINECS 213-221-4
T0MIX7SJ2E
Imidazole, 2,4-dimethyl-
NSC-13192
MFCD00022365
2,4-dimethyl-imidazole
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2,4-Dimethylimidazole

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 - 0.5760 57.60%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.8429 84.29%
Subcellular localzation Lysosomes 0.4045 40.45%
OATP2B1 inhibitior - 0.8773 87.73%
OATP1B1 inhibitior + 0.9700 97.00%
OATP1B3 inhibitior + 0.9535 95.35%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8940 89.40%
P-glycoprotein inhibitior - 0.9852 98.52%
P-glycoprotein substrate - 0.9745 97.45%
CYP3A4 substrate - 0.7349 73.49%
CYP2C9 substrate - 0.8110 81.10%
CYP2D6 substrate - 0.8753 87.53%
CYP3A4 inhibition - 0.9583 95.83%
CYP2C9 inhibition - 0.9412 94.12%
CYP2C19 inhibition - 0.8072 80.72%
CYP2D6 inhibition - 0.9378 93.78%
CYP1A2 inhibition - 0.7726 77.26%
CYP2C8 inhibition - 0.9148 91.48%
CYP inhibitory promiscuity - 0.9158 91.58%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Warning 0.5079 50.79%
Eye corrosion + 0.9409 94.09%
Eye irritation + 0.9764 97.64%
Skin irritation + 0.7001 70.01%
Skin corrosion + 0.9167 91.67%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7582 75.82%
Micronuclear + 0.7700 77.00%
Hepatotoxicity + 0.7750 77.50%
skin sensitisation - 0.9379 93.79%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity - 0.5811 58.11%
Acute Oral Toxicity (c) III 0.7085 70.85%
Estrogen receptor binding - 0.9620 96.20%
Androgen receptor binding - 0.9589 95.89%
Thyroid receptor binding - 0.8680 86.80%
Glucocorticoid receptor binding - 0.9340 93.40%
Aromatase binding - 0.8990 89.90%
PPAR gamma - 0.9022 90.22%
Honey bee toxicity - 0.9622 96.22%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity - 0.8779 87.79%

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 86.09% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 85.70% 94.73%
CHEMBL1937 Q92769 Histone deacetylase 2 84.10% 94.75%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 83.72% 93.65%
CHEMBL3310 Q96DB2 Histone deacetylase 11 82.88% 88.56%
CHEMBL2292 Q13627 Dual-specificity tyrosine-phosphorylation regulated kinase 1A 82.83% 93.24%
CHEMBL2424504 P29375 Lysine-specific demethylase 5A 80.98% 99.23%

Cross-Links

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PubChem 70259
NPASS NPC246810
LOTUS LTS0246759
wikiData Q72470633