2,3-Dimethyl-6-isopropyl-4h-pyran

Details

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Internal ID e87842a5-d8f3-45f8-b161-37f15264a0b6
Taxonomy Organoheterocyclic compounds > Pyrans
IUPAC Name 2,3-dimethyl-6-propan-2-yl-4H-pyran
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H16O/c1-7(2)10-6-5-8(3)9(4)11-10/h6-7H,5H2,1-4H3
InChI Key SWNKFDXTSKNDOZ-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16O
Molecular Weight 152.23 g/mol
Exact Mass 152.120115130 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 2.60
Atomic LogP (AlogP) 3.24
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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

2D Structure

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2D Structure of 2,3-Dimethyl-6-isopropyl-4h-pyran

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9910 99.10%
Caco-2 + 0.7508 75.08%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Lysosomes 0.4025 40.25%
OATP2B1 inhibitior - 0.8555 85.55%
OATP1B1 inhibitior + 0.9592 95.92%
OATP1B3 inhibitior + 0.9383 93.83%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8897 88.97%
P-glycoprotein inhibitior - 0.9717 97.17%
P-glycoprotein substrate - 0.9524 95.24%
CYP3A4 substrate - 0.7025 70.25%
CYP2C9 substrate - 0.6092 60.92%
CYP2D6 substrate - 0.7180 71.80%
CYP3A4 inhibition - 0.9128 91.28%
CYP2C9 inhibition - 0.7914 79.14%
CYP2C19 inhibition - 0.6373 63.73%
CYP2D6 inhibition - 0.9212 92.12%
CYP1A2 inhibition - 0.5219 52.19%
CYP2C8 inhibition - 0.9731 97.31%
CYP inhibitory promiscuity - 0.5426 54.26%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6444 64.44%
Carcinogenicity (trinary) Non-required 0.5039 50.39%
Eye corrosion - 0.8014 80.14%
Eye irritation + 0.9084 90.84%
Skin irritation + 0.7423 74.23%
Skin corrosion - 0.9199 91.99%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5666 56.66%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.7125 71.25%
skin sensitisation + 0.7631 76.31%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity - 0.5889 58.89%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity + 0.4567 45.67%
Acute Oral Toxicity (c) III 0.7359 73.59%
Estrogen receptor binding - 0.9622 96.22%
Androgen receptor binding - 0.7733 77.33%
Thyroid receptor binding - 0.8735 87.35%
Glucocorticoid receptor binding - 0.8934 89.34%
Aromatase binding - 0.8797 87.97%
PPAR gamma - 0.9009 90.09%
Honey bee toxicity - 0.9248 92.48%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.8888 88.88%

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 89.80% 98.95%
CHEMBL3359 P21462 Formyl peptide receptor 1 89.54% 93.56%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 88.47% 93.65%
CHEMBL3401 O75469 Pregnane X receptor 86.03% 94.73%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 83.48% 86.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.97% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.76% 95.56%

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 12070933
LOTUS LTS0149159
wikiData Q105262763