5-Dodec-1-enyl-1,3-benzodioxole

Details

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Internal ID c5787d1b-ce3b-4f9e-aabe-e854eff22d6f
Taxonomy Organoheterocyclic compounds > Benzodioxoles
IUPAC Name 5-dodec-1-enyl-1,3-benzodioxole
SMILES (Canonical) CCCCCCCCCCC=CC1=CC2=C(C=C1)OCO2
SMILES (Isomeric) CCCCCCCCCCC=CC1=CC2=C(C=C1)OCO2
InChI InChI=1S/C19H28O2/c1-2-3-4-5-6-7-8-9-10-11-12-17-13-14-18-19(15-17)21-16-20-18/h11-15H,2-10,16H2,1H3
InChI Key CXFWEZQTIXOIEV-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C19H28O2
Molecular Weight 288.40 g/mol
Exact Mass 288.208930132 g/mol
Topological Polar Surface Area (TPSA) 18.50 Ų
XlogP 7.90
Atomic LogP (AlogP) 5.96
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-Dodec-1-enyl-1,3-benzodioxole

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.9357 93.57%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Plasma membrane 0.5804 58.04%
OATP2B1 inhibitior - 0.8585 85.85%
OATP1B1 inhibitior + 0.8876 88.76%
OATP1B3 inhibitior + 0.9405 94.05%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.8524 85.24%
P-glycoprotein inhibitior - 0.5351 53.51%
P-glycoprotein substrate - 0.8964 89.64%
CYP3A4 substrate - 0.6174 61.74%
CYP2C9 substrate + 0.5499 54.99%
CYP2D6 substrate - 0.7169 71.69%
CYP3A4 inhibition + 0.5000 50.00%
CYP2C9 inhibition - 0.6230 62.30%
CYP2C19 inhibition + 0.6902 69.02%
CYP2D6 inhibition - 0.6052 60.52%
CYP1A2 inhibition + 0.8177 81.77%
CYP2C8 inhibition - 0.8193 81.93%
CYP inhibitory promiscuity + 0.7883 78.83%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.4472 44.72%
Eye corrosion - 0.9431 94.31%
Eye irritation + 0.8954 89.54%
Skin irritation - 0.5187 51.87%
Skin corrosion - 0.9035 90.35%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8750 87.50%
Micronuclear - 0.8500 85.00%
Hepatotoxicity - 0.5467 54.67%
skin sensitisation + 0.6148 61.48%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.5082 50.82%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity - 0.7153 71.53%
Acute Oral Toxicity (c) III 0.7802 78.02%
Estrogen receptor binding + 0.7134 71.34%
Androgen receptor binding + 0.9232 92.32%
Thyroid receptor binding + 0.7812 78.12%
Glucocorticoid receptor binding - 0.7184 71.84%
Aromatase binding - 0.6001 60.01%
PPAR gamma + 0.6807 68.07%
Honey bee toxicity - 0.9726 97.26%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.8253 82.53%
Fish aquatic toxicity + 0.9927 99.27%

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
CHEMBL240 Q12809 HERG 99.52% 89.76%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.26% 91.11%
CHEMBL230 P35354 Cyclooxygenase-2 96.45% 89.63%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 96.21% 94.80%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 95.84% 92.08%
CHEMBL2581 P07339 Cathepsin D 95.73% 98.95%
CHEMBL2039 P27338 Monoamine oxidase B 95.12% 92.51%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.80% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.07% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 93.27% 96.00%
CHEMBL1951 P21397 Monoamine oxidase A 91.95% 91.49%
CHEMBL3401 O75469 Pregnane X receptor 90.22% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.01% 94.45%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 87.96% 96.77%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 87.77% 85.30%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.73% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.77% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.62% 89.00%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 83.26% 91.81%
CHEMBL3192 Q9BY41 Histone deacetylase 8 82.67% 93.99%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 82.04% 89.62%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 81.94% 80.96%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.59% 92.62%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.58% 100.00%

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.
Barleria prionitis
Piper sintenense

Cross-Links

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PubChem 69542164
LOTUS LTS0091468
wikiData Q104971843