6-methyl-2-propan-2-yl-1H-pyrimidin-4-one

Details

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Internal ID 7ba702e7-3720-43f3-bd2c-79e0f06f2fc7
Taxonomy Organoheterocyclic compounds > Diazines > Pyrimidines and pyrimidine derivatives > Hydroxypyrimidines
IUPAC Name 6-methyl-2-propan-2-yl-1H-pyrimidin-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H12N2O/c1-5(2)8-9-6(3)4-7(11)10-8/h4-5H,1-3H3,(H,9,10,11)
InChI Key AJPIUNPJBFBUKK-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C8H12N2O
Molecular Weight 152.19 g/mol
Exact Mass 152.094963011 g/mol
Topological Polar Surface Area (TPSA) 41.50 Ų
XlogP 0.70
Atomic LogP (AlogP) 1.20
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-methyl-2-propan-2-yl-1H-pyrimidin-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9970 99.70%
Caco-2 - 0.6780 67.80%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Mitochondria 0.7504 75.04%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9603 96.03%
OATP1B3 inhibitior + 0.9538 95.38%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9164 91.64%
P-glycoprotein inhibitior - 0.9547 95.47%
P-glycoprotein substrate - 0.9698 96.98%
CYP3A4 substrate - 0.6784 67.84%
CYP2C9 substrate - 0.6061 60.61%
CYP2D6 substrate - 0.9125 91.25%
CYP3A4 inhibition - 0.9915 99.15%
CYP2C9 inhibition - 0.9472 94.72%
CYP2C19 inhibition - 0.9568 95.68%
CYP2D6 inhibition - 0.9741 97.41%
CYP1A2 inhibition - 0.5000 50.00%
CYP2C8 inhibition - 0.9727 97.27%
CYP inhibitory promiscuity - 0.9800 98.00%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8923 89.23%
Carcinogenicity (trinary) Non-required 0.5836 58.36%
Eye corrosion - 0.9673 96.73%
Eye irritation + 0.8883 88.83%
Skin irritation - 0.7737 77.37%
Skin corrosion - 0.9307 93.07%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6984 69.84%
Micronuclear + 0.6500 65.00%
Hepatotoxicity + 0.7625 76.25%
skin sensitisation - 0.8108 81.08%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity + 0.5618 56.18%
Acute Oral Toxicity (c) III 0.7356 73.56%
Estrogen receptor binding - 0.9552 95.52%
Androgen receptor binding - 0.7611 76.11%
Thyroid receptor binding - 0.6297 62.97%
Glucocorticoid receptor binding - 0.9233 92.33%
Aromatase binding - 0.8487 84.87%
PPAR gamma - 0.9151 91.51%
Honey bee toxicity - 0.9667 96.67%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity - 0.9011 90.11%

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
CHEMBL2581 P07339 Cathepsin D 92.26% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.13% 85.14%
CHEMBL1937 Q92769 Histone deacetylase 2 90.91% 94.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.16% 95.56%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 87.16% 93.40%
CHEMBL3401 O75469 Pregnane X receptor 87.03% 94.73%
CHEMBL2424504 P29375 Lysine-specific demethylase 5A 85.92% 99.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.73% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.24% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.99% 99.23%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.69% 99.15%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.10% 90.71%
CHEMBL2535 P11166 Glucose transporter 81.84% 98.75%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 80.35% 93.65%

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.
Cichorium pumilum

Cross-Links

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PubChem 17777
LOTUS LTS0050111
wikiData Q27889436