6-Isopropenyl-2,2-dimethyl-2H-pyran

Details

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Internal ID 7624d1d2-dfd2-4e05-ac30-b50353e95cb8
Taxonomy Organoheterocyclic compounds > Pyrans
IUPAC Name 2,2-dimethyl-6-prop-1-en-2-ylpyran
SMILES (Canonical) CC(=C)C1=CC=CC(O1)(C)C
SMILES (Isomeric) CC(=C)C1=CC=CC(O1)(C)C
InChI InChI=1S/C10H14O/c1-8(2)9-6-5-7-10(3,4)11-9/h5-7H,1H2,2-4H3
InChI Key HNVSTMZBBLAYKR-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C10H14O
Molecular Weight 150.22 g/mol
Exact Mass 150.104465066 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.81
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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2,2-dimethyl-6-prop-1-en-2-ylpyran
2,2-Dimethyl-6-isopropenyl-2H-pyran
InChI=1/C10H14O/c1-8(2)9-6-5-7-10(3,4)11-9/h5-7H,1H2,2-4H

2D Structure

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2D Structure of 6-Isopropenyl-2,2-dimethyl-2H-pyran

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9825 98.25%
Caco-2 + 0.8835 88.35%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.4578 45.78%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9094 90.94%
OATP1B3 inhibitior + 0.9532 95.32%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9080 90.80%
P-glycoprotein inhibitior - 0.9731 97.31%
P-glycoprotein substrate - 0.9483 94.83%
CYP3A4 substrate - 0.5992 59.92%
CYP2C9 substrate + 0.6200 62.00%
CYP2D6 substrate - 0.7942 79.42%
CYP3A4 inhibition - 0.5893 58.93%
CYP2C9 inhibition - 0.6595 65.95%
CYP2C19 inhibition + 0.5702 57.02%
CYP2D6 inhibition - 0.9347 93.47%
CYP1A2 inhibition - 0.6273 62.73%
CYP2C8 inhibition - 0.8943 89.43%
CYP inhibitory promiscuity + 0.5000 50.00%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6363 63.63%
Carcinogenicity (trinary) Non-required 0.4950 49.50%
Eye corrosion + 0.5605 56.05%
Eye irritation + 0.9923 99.23%
Skin irritation + 0.7467 74.67%
Skin corrosion - 0.9194 91.94%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5225 52.25%
Micronuclear - 0.8200 82.00%
Hepatotoxicity + 0.7354 73.54%
skin sensitisation + 0.8183 81.83%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity - 0.7000 70.00%
Mitochondrial toxicity - 0.8446 84.46%
Nephrotoxicity + 0.6066 60.66%
Acute Oral Toxicity (c) III 0.7811 78.11%
Estrogen receptor binding - 0.9140 91.40%
Androgen receptor binding - 0.9530 95.30%
Thyroid receptor binding - 0.8539 85.39%
Glucocorticoid receptor binding - 0.9076 90.76%
Aromatase binding - 0.8669 86.69%
PPAR gamma - 0.8704 87.04%
Honey bee toxicity - 0.8660 86.60%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.6602 66.02%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.31% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.69% 96.09%
CHEMBL1951 P21397 Monoamine oxidase A 86.76% 91.49%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.67% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 82.33% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.03% 86.33%

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 cana

Cross-Links

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PubChem 636526
LOTUS LTS0225869
wikiData Q105031088