2,4,5-Trimethyloxazole

Details

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Internal ID 09fccf05-67b7-4863-910e-de907f520c2e
Taxonomy Organoheterocyclic compounds > Azoles > Oxazoles > 2,4,5-trisubstituted oxazoles
IUPAC Name 2,4,5-trimethyl-1,3-oxazole
SMILES (Canonical) CC1=C(OC(=N1)C)C
SMILES (Isomeric) CC1=C(OC(=N1)C)C
InChI InChI=1S/C6H9NO/c1-4-5(2)8-6(3)7-4/h1-3H3
InChI Key ZRLDBDZSLLGDOX-UHFFFAOYSA-N
Popularity 50 references in papers

Physical and Chemical Properties

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Molecular Formula C6H9NO
Molecular Weight 111.14 g/mol
Exact Mass 111.068413911 g/mol
Topological Polar Surface Area (TPSA) 26.00 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.60
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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2,4,5-TRIMETHYLOXAZOLE
20662-84-4
Trimethyloxazole
Oxazole, trimethyl-
2,4,5-Trimethyl-1,3-oxazole
Oxazole, 2,4,5-trimethyl-
trimethyl-1,3-oxazole
B04PF51WXI
Oxazole, 2,4,5-trimethyl
EINECS 243-952-4
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2,4,5-Trimethyloxazole

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9904 99.04%
Caco-2 - 0.5961 59.61%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.5656 56.56%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9701 97.01%
OATP1B3 inhibitior + 0.9542 95.42%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8796 87.96%
P-glycoprotein inhibitior - 0.9702 97.02%
P-glycoprotein substrate - 0.9731 97.31%
CYP3A4 substrate - 0.7217 72.17%
CYP2C9 substrate - 0.8058 80.58%
CYP2D6 substrate - 0.8487 84.87%
CYP3A4 inhibition - 0.9551 95.51%
CYP2C9 inhibition - 0.9064 90.64%
CYP2C19 inhibition - 0.7256 72.56%
CYP2D6 inhibition - 0.9171 91.71%
CYP1A2 inhibition + 0.6804 68.04%
CYP2C8 inhibition - 0.9699 96.99%
CYP inhibitory promiscuity + 0.5686 56.86%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Non-required 0.3915 39.15%
Eye corrosion - 0.9124 91.24%
Eye irritation + 0.9753 97.53%
Skin irritation - 0.6072 60.72%
Skin corrosion - 0.9571 95.71%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7848 78.48%
Micronuclear - 0.5700 57.00%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation - 0.8670 86.70%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity + 0.7272 72.72%
Acute Oral Toxicity (c) III 0.6466 64.66%
Estrogen receptor binding - 0.9174 91.74%
Androgen receptor binding - 0.8928 89.28%
Thyroid receptor binding - 0.6651 66.51%
Glucocorticoid receptor binding - 0.8785 87.85%
Aromatase binding - 0.7701 77.01%
PPAR gamma - 0.8670 86.70%
Honey bee toxicity - 0.9690 96.90%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.6500 65.00%
Fish aquatic toxicity - 0.9399 93.99%

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 89.48% 94.73%
CHEMBL235 P37231 Peroxisome proliferator-activated receptor gamma 88.86% 95.39%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 88.10% 93.65%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 83.70% 81.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.83% 94.00%

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.
There are no matching plants.

Cross-Links

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PubChem 30215
LOTUS LTS0066145
wikiData Q27274214