4-(2-Hydroxyethyl)-5-methyloxazole

Details

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Internal ID 11c4497b-3649-47ee-8f6a-9ace7bc46018
Taxonomy Organoheterocyclic compounds > Azoles > Oxazoles > 4,5-disubstituted oxazoles
IUPAC Name 2-(5-methyl-1,3-oxazol-4-yl)ethanol
SMILES (Canonical) CC1=C(N=CO1)CCO
SMILES (Isomeric) CC1=C(N=CO1)CCO
InChI InChI=1S/C6H9NO2/c1-5-6(2-3-8)7-4-9-5/h4,8H,2-3H2,1H3
InChI Key QFOLRXLMTRGIOM-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C6H9NO2
Molecular Weight 127.14 g/mol
Exact Mass 127.063328530 g/mol
Topological Polar Surface Area (TPSA) 46.30 Ų
XlogP 0.30
Atomic LogP (AlogP) 0.52
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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4-(2-hydroxyethyl)-5-methyloxazole

2D Structure

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2D Structure of 4-(2-Hydroxyethyl)-5-methyloxazole

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9964 99.64%
Caco-2 + 0.6390 63.90%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.6359 63.59%
OATP2B1 inhibitior - 0.8602 86.02%
OATP1B1 inhibitior + 0.9213 92.13%
OATP1B3 inhibitior + 0.9426 94.26%
MATE1 inhibitior - 0.9012 90.12%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.9121 91.21%
P-glycoprotein inhibitior - 0.9865 98.65%
P-glycoprotein substrate - 0.9401 94.01%
CYP3A4 substrate - 0.6596 65.96%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8096 80.96%
CYP3A4 inhibition - 0.9627 96.27%
CYP2C9 inhibition - 0.8695 86.95%
CYP2C19 inhibition - 0.7386 73.86%
CYP2D6 inhibition - 0.9155 91.55%
CYP1A2 inhibition - 0.7153 71.53%
CYP2C8 inhibition - 0.8464 84.64%
CYP inhibitory promiscuity - 0.9045 90.45%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8200 82.00%
Carcinogenicity (trinary) Non-required 0.5616 56.16%
Eye corrosion - 0.9731 97.31%
Eye irritation + 0.9635 96.35%
Skin irritation - 0.6711 67.11%
Skin corrosion - 0.8388 83.88%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5571 55.71%
Micronuclear - 0.6800 68.00%
Hepatotoxicity + 0.5731 57.31%
skin sensitisation - 0.8304 83.04%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity + 0.6201 62.01%
Acute Oral Toxicity (c) III 0.6321 63.21%
Estrogen receptor binding - 0.9387 93.87%
Androgen receptor binding - 0.6593 65.93%
Thyroid receptor binding - 0.8810 88.10%
Glucocorticoid receptor binding - 0.9175 91.75%
Aromatase binding - 0.8530 85.30%
PPAR gamma - 0.8770 87.70%
Honey bee toxicity - 0.9741 97.41%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.8300 83.00%
Fish aquatic toxicity - 0.9855 98.55%

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 91.14% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.13% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.81% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.50% 94.00%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 81.95% 93.65%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.55% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.41% 96.00%

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.
Equisetum hyemale

Cross-Links

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PubChem 22926318
NPASS NPC241509
LOTUS LTS0018732
wikiData Q77484466