2-Pentadec-1-enylfuran

Details

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Internal ID b7fdc500-87d2-4716-a69c-1aa4eafbb2ad
Taxonomy Organoheterocyclic compounds > Heteroaromatic compounds
IUPAC Name 2-pentadec-1-enylfuran
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H32O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-16-19-17-15-18-20-19/h14-18H,2-13H2,1H3
InChI Key MAGFAZWZYBRMGQ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H32O
Molecular Weight 276.50 g/mol
Exact Mass 276.245315640 g/mol
Topological Polar Surface Area (TPSA) 13.10 Ų
XlogP 8.40
Atomic LogP (AlogP) 6.99
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 13

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Pentadec-1-enylfuran

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9960 99.60%
Caco-2 + 0.8777 87.77%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Plasma membrane 0.6545 65.45%
OATP2B1 inhibitior - 0.8583 85.83%
OATP1B1 inhibitior + 0.8581 85.81%
OATP1B3 inhibitior + 0.9476 94.76%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.6974 69.74%
P-glycoprotein inhibitior - 0.8315 83.15%
P-glycoprotein substrate - 0.8860 88.60%
CYP3A4 substrate - 0.6161 61.61%
CYP2C9 substrate + 0.6012 60.12%
CYP2D6 substrate - 0.7270 72.70%
CYP3A4 inhibition - 0.9608 96.08%
CYP2C9 inhibition - 0.7823 78.23%
CYP2C19 inhibition - 0.5270 52.70%
CYP2D6 inhibition - 0.8908 89.08%
CYP1A2 inhibition + 0.7037 70.37%
CYP2C8 inhibition - 0.7317 73.17%
CYP inhibitory promiscuity + 0.6951 69.51%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8200 82.00%
Carcinogenicity (trinary) Non-required 0.3648 36.48%
Eye corrosion + 0.7159 71.59%
Eye irritation + 0.8389 83.89%
Skin irritation + 0.8044 80.44%
Skin corrosion - 0.9065 90.65%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8962 89.62%
Micronuclear - 0.9200 92.00%
Hepatotoxicity - 0.6891 68.91%
skin sensitisation + 0.7840 78.40%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.5087 50.87%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity - 0.5734 57.34%
Acute Oral Toxicity (c) III 0.7796 77.96%
Estrogen receptor binding + 0.8521 85.21%
Androgen receptor binding - 0.7511 75.11%
Thyroid receptor binding + 0.7103 71.03%
Glucocorticoid receptor binding - 0.6414 64.14%
Aromatase binding + 0.5761 57.61%
PPAR gamma + 0.8279 82.79%
Honey bee toxicity - 0.9914 99.14%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity + 0.7953 79.53%
Fish aquatic toxicity + 0.9714 97.14%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 94.74% 92.08%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.61% 99.17%
CHEMBL2581 P07339 Cathepsin D 93.41% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.21% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 92.22% 94.73%
CHEMBL230 P35354 Cyclooxygenase-2 90.73% 89.63%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.85% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.75% 95.56%
CHEMBL1781 P11387 DNA topoisomerase I 86.22% 97.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.29% 96.00%
CHEMBL1951 P21397 Monoamine oxidase A 85.06% 91.49%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.89% 96.09%
CHEMBL240 Q12809 HERG 83.59% 89.76%
CHEMBL221 P23219 Cyclooxygenase-1 83.52% 90.17%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.98% 93.56%
CHEMBL1907 P15144 Aminopeptidase N 81.80% 93.31%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 80.10% 85.94%

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.
Persea indica

Cross-Links

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PubChem 54061814
LOTUS LTS0202166
wikiData Q105160317