1,3-Dioxolane, 2-heptyl-4-phenyl-

Details

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Internal ID f5508760-1a8b-4b95-9b84-d5a9b4763560
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name 2-heptyl-4-phenyl-1,3-dioxolane
SMILES (Canonical) CCCCCCCC1OCC(O1)C2=CC=CC=C2
SMILES (Isomeric) CCCCCCCC1OCC(O1)C2=CC=CC=C2
InChI InChI=1S/C16H24O2/c1-2-3-4-5-9-12-16-17-13-15(18-16)14-10-7-6-8-11-14/h6-8,10-11,15-16H,2-5,9,12-13H2,1H3
InChI Key RQCDWZAGEAEBOX-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H24O2
Molecular Weight 248.36 g/mol
Exact Mass 248.177630004 g/mol
Topological Polar Surface Area (TPSA) 18.50 Ų
XlogP 4.80
Atomic LogP (AlogP) 4.46
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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1,3-Dioxolane, 2-heptyl-4-phenyl-
2-Heptyl-4-phenyl-1,3-dioxolane #

2D Structure

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2D Structure of 1,3-Dioxolane, 2-heptyl-4-phenyl-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9971 99.71%
Caco-2 + 0.8511 85.11%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.5134 51.34%
OATP2B1 inhibitior - 0.8586 85.86%
OATP1B1 inhibitior + 0.9007 90.07%
OATP1B3 inhibitior + 0.9269 92.69%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.7005 70.05%
P-glycoprotein inhibitior - 0.8542 85.42%
P-glycoprotein substrate - 0.7429 74.29%
CYP3A4 substrate - 0.5899 58.99%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7070 70.70%
CYP3A4 inhibition - 0.8527 85.27%
CYP2C9 inhibition - 0.6759 67.59%
CYP2C19 inhibition - 0.5000 50.00%
CYP2D6 inhibition - 0.8693 86.93%
CYP1A2 inhibition + 0.5160 51.60%
CYP2C8 inhibition + 0.5414 54.14%
CYP inhibitory promiscuity + 0.5633 56.33%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.5115 51.15%
Eye corrosion - 0.8636 86.36%
Eye irritation - 0.6150 61.50%
Skin irritation - 0.5467 54.67%
Skin corrosion - 0.9463 94.63%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8738 87.38%
Micronuclear - 0.8700 87.00%
Hepatotoxicity - 0.6625 66.25%
skin sensitisation - 0.7878 78.78%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.5193 51.93%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity - 0.6159 61.59%
Acute Oral Toxicity (c) III 0.8235 82.35%
Estrogen receptor binding - 0.4931 49.31%
Androgen receptor binding - 0.6108 61.08%
Thyroid receptor binding - 0.5446 54.46%
Glucocorticoid receptor binding - 0.8144 81.44%
Aromatase binding - 0.7524 75.24%
PPAR gamma - 0.5284 52.84%
Honey bee toxicity - 0.9825 98.25%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.6072 60.72%
Fish aquatic toxicity + 0.9433 94.33%

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 96.10% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.36% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.67% 91.11%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 91.27% 92.08%
CHEMBL221 P23219 Cyclooxygenase-1 89.54% 90.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.50% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.24% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 88.69% 94.73%
CHEMBL230 P35354 Cyclooxygenase-2 87.05% 89.63%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.62% 95.56%
CHEMBL2996 Q05655 Protein kinase C delta 82.34% 97.79%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.46% 99.17%

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.
Citrus × aurantium
Citrus deliciosa

Cross-Links

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PubChem 558638
NPASS NPC211171