5-Undecyl-1,3-benzodioxole

Details

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Internal ID 78a10927-d054-4f06-a915-cd24716f6574
Taxonomy Organoheterocyclic compounds > Benzodioxoles
IUPAC Name 5-undecyl-1,3-benzodioxole
SMILES (Canonical) CCCCCCCCCCCC1=CC2=C(C=C1)OCO2
SMILES (Isomeric) CCCCCCCCCCCC1=CC2=C(C=C1)OCO2
InChI InChI=1S/C18H28O2/c1-2-3-4-5-6-7-8-9-10-11-16-12-13-17-18(14-16)20-15-19-17/h12-14H,2-11,15H2,1H3
InChI Key WPKSHCKNVIUZMF-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H28O2
Molecular Weight 276.40 g/mol
Exact Mass 276.208930132 g/mol
Topological Polar Surface Area (TPSA) 18.50 Ų
XlogP 7.60
Atomic LogP (AlogP) 5.49
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-Undecyl-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 + 0.9422 94.22%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.4421 44.21%
OATP2B1 inhibitior - 0.8563 85.63%
OATP1B1 inhibitior + 0.9259 92.59%
OATP1B3 inhibitior + 0.9414 94.14%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.8262 82.62%
P-glycoprotein inhibitior - 0.6707 67.07%
P-glycoprotein substrate - 0.8018 80.18%
CYP3A4 substrate - 0.6060 60.60%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3586 35.86%
CYP3A4 inhibition + 0.5077 50.77%
CYP2C9 inhibition - 0.5864 58.64%
CYP2C19 inhibition + 0.6967 69.67%
CYP2D6 inhibition - 0.6069 60.69%
CYP1A2 inhibition + 0.8241 82.41%
CYP2C8 inhibition - 0.7490 74.90%
CYP inhibitory promiscuity + 0.6471 64.71%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.4508 45.08%
Eye corrosion - 0.9330 93.30%
Eye irritation + 0.9376 93.76%
Skin irritation - 0.5576 55.76%
Skin corrosion - 0.9002 90.02%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8424 84.24%
Micronuclear - 0.8600 86.00%
Hepatotoxicity - 0.5393 53.93%
skin sensitisation + 0.5542 55.42%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.5193 51.93%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity - 0.5813 58.13%
Acute Oral Toxicity (c) III 0.7871 78.71%
Estrogen receptor binding + 0.8586 85.86%
Androgen receptor binding + 0.8494 84.94%
Thyroid receptor binding + 0.7951 79.51%
Glucocorticoid receptor binding - 0.6378 63.78%
Aromatase binding - 0.5000 50.00%
PPAR gamma - 0.4871 48.71%
Honey bee toxicity - 0.9776 97.76%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.8103 81.03%
Fish aquatic toxicity + 0.9823 98.23%

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 98.70% 89.76%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 98.03% 94.80%
CHEMBL2581 P07339 Cathepsin D 97.99% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 96.84% 92.08%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 95.33% 96.77%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.48% 94.45%
CHEMBL2039 P27338 Monoamine oxidase B 92.40% 92.51%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.25% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.78% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.63% 96.09%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 89.33% 95.17%
CHEMBL5805 Q9NR97 Toll-like receptor 8 89.29% 96.25%
CHEMBL3401 O75469 Pregnane X receptor 89.03% 94.73%
CHEMBL230 P35354 Cyclooxygenase-2 88.46% 89.63%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.16% 99.17%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 86.68% 92.86%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 85.07% 80.96%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 84.88% 100.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.81% 92.62%

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.
Piper longum

Cross-Links

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PubChem 5315124
NPASS NPC8483