2-Hydroxy-5-methylpyridine

Details

Top
Internal ID 32441b2f-6d96-433c-b633-9045e3d00eee
Taxonomy Organoheterocyclic compounds > Pyridines and derivatives > Hydropyridines > Pyridinones
IUPAC Name 5-methyl-1H-pyridin-2-one
SMILES (Canonical) CC1=CNC(=O)C=C1
SMILES (Isomeric) CC1=CNC(=O)C=C1
InChI InChI=1S/C6H7NO/c1-5-2-3-6(8)7-4-5/h2-4H,1H3,(H,7,8)
InChI Key SOHMZGMHXUQHGE-UHFFFAOYSA-N
Popularity 18 references in papers

Physical and Chemical Properties

Top
Molecular Formula C6H7NO
Molecular Weight 109.13 g/mol
Exact Mass 109.052763847 g/mol
Topological Polar Surface Area (TPSA) 29.10 Ų
XlogP 0.10
Atomic LogP (AlogP) 0.68
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

Top
1003-68-5
5-Methyl-2-pyridone
5-Methyl-2(1H)-pyridinone
C173P2D70Y
DTXSID20143120
RefChem:537051
DTXCID3065611
213-713-9
5-methylpyridin-2-ol
91914-06-6
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of 2-Hydroxy-5-methylpyridine

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.6730 67.30%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Mitochondria 0.6544 65.44%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9686 96.86%
OATP1B3 inhibitior + 0.9674 96.74%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.8595 85.95%
P-glycoprotein inhibitior - 0.9860 98.60%
P-glycoprotein substrate - 0.9852 98.52%
CYP3A4 substrate - 0.7583 75.83%
CYP2C9 substrate - 0.6091 60.91%
CYP2D6 substrate - 0.8841 88.41%
CYP3A4 inhibition - 0.9795 97.95%
CYP2C9 inhibition - 0.9804 98.04%
CYP2C19 inhibition - 0.9830 98.30%
CYP2D6 inhibition - 0.9737 97.37%
CYP1A2 inhibition - 0.7150 71.50%
CYP2C8 inhibition - 0.9939 99.39%
CYP inhibitory promiscuity - 0.9737 97.37%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7723 77.23%
Carcinogenicity (trinary) Non-required 0.5687 56.87%
Eye corrosion - 0.7578 75.78%
Eye irritation + 0.9907 99.07%
Skin irritation + 0.7401 74.01%
Skin corrosion - 0.9221 92.21%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7686 76.86%
Micronuclear + 0.6600 66.00%
Hepatotoxicity + 0.7375 73.75%
skin sensitisation - 0.5996 59.96%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity + 0.5236 52.36%
Acute Oral Toxicity (c) III 0.8272 82.72%
Estrogen receptor binding - 0.9638 96.38%
Androgen receptor binding - 0.9700 97.00%
Thyroid receptor binding - 0.8901 89.01%
Glucocorticoid receptor binding - 0.8899 88.99%
Aromatase binding - 0.9031 90.31%
PPAR gamma - 0.8452 84.52%
Honey bee toxicity - 0.9605 96.05%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity - 0.9240 92.40%

Targets

Top

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.74% 95.56%
CHEMBL2581 P07339 Cathepsin D 92.96% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 82.40% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.12% 94.45%

Plants that contains it

Top
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.
Syzygium aromaticum

Cross-Links

Top
PubChem 70482
NPASS NPC6488