2,2-dimethyl-6-propan-2-yl-3H-pyran-4-one

Details

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Internal ID a0c1f6d2-0eec-4c18-8714-b6766b7599cf
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives > Dihydropyranones
IUPAC Name 2,2-dimethyl-6-propan-2-yl-3H-pyran-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H16O2/c1-7(2)9-5-8(11)6-10(3,4)12-9/h5,7H,6H2,1-4H3
InChI Key ZBGHKXZWQJSFAC-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16O2
Molecular Weight 168.23 g/mol
Exact Mass 168.115029749 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 1.70
Atomic LogP (AlogP) 2.29
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,2-dimethyl-6-propan-2-yl-3H-pyran-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 + 0.9931 99.31%
Caco-2 + 0.8746 87.46%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.6984 69.84%
OATP2B1 inhibitior - 0.8565 85.65%
OATP1B1 inhibitior + 0.9271 92.71%
OATP1B3 inhibitior + 0.9791 97.91%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9550 95.50%
P-glycoprotein inhibitior - 0.9452 94.52%
P-glycoprotein substrate - 0.9576 95.76%
CYP3A4 substrate - 0.5943 59.43%
CYP2C9 substrate - 0.8111 81.11%
CYP2D6 substrate - 0.8582 85.82%
CYP3A4 inhibition - 0.8377 83.77%
CYP2C9 inhibition - 0.8594 85.94%
CYP2C19 inhibition - 0.6190 61.90%
CYP2D6 inhibition - 0.9272 92.72%
CYP1A2 inhibition - 0.6852 68.52%
CYP2C8 inhibition - 0.9879 98.79%
CYP inhibitory promiscuity - 0.8478 84.78%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7659 76.59%
Carcinogenicity (trinary) Warning 0.4599 45.99%
Eye corrosion - 0.6165 61.65%
Eye irritation + 0.9423 94.23%
Skin irritation + 0.6593 65.93%
Skin corrosion - 0.8998 89.98%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7212 72.12%
Micronuclear - 0.7300 73.00%
Hepatotoxicity + 0.6677 66.77%
skin sensitisation + 0.8153 81.53%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity - 0.7444 74.44%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity + 0.7569 75.69%
Acute Oral Toxicity (c) III 0.7263 72.63%
Estrogen receptor binding - 0.9018 90.18%
Androgen receptor binding - 0.8056 80.56%
Thyroid receptor binding - 0.8607 86.07%
Glucocorticoid receptor binding - 0.8781 87.81%
Aromatase binding - 0.7910 79.10%
PPAR gamma - 0.9121 91.21%
Honey bee toxicity - 0.9208 92.08%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity - 0.5873 58.73%

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
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 95.06% 96.77%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.79% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.96% 98.95%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 90.01% 85.30%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.75% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.11% 95.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.10% 90.71%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.14% 97.25%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.81% 99.23%

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.
Artemisia tridentata

Cross-Links

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PubChem 13611567
LOTUS LTS0262094
wikiData Q105370578