2-[(E)-tridec-1-en-12-ynyl]furan

Details

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Internal ID 45dcb8a0-ee57-4f56-b42d-9e62365fac72
Taxonomy Organoheterocyclic compounds > Heteroaromatic compounds
IUPAC Name 2-[(E)-tridec-1-en-12-ynyl]furan
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H24O/c1-2-3-4-5-6-7-8-9-10-11-12-14-17-15-13-16-18-17/h1,12-16H,3-11H2/b14-12+
InChI Key MAVLUNCWNSBXOR-WYMLVPIESA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C17H24O
Molecular Weight 244.37 g/mol
Exact Mass 244.182715385 g/mol
Topological Polar Surface Area (TPSA) 13.10 Ų
XlogP 6.30
Atomic LogP (AlogP) 5.44
H-Bond Acceptor 1
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 2-[(E)-tridec-1-en-12-ynyl]furan

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9907 99.07%
Caco-2 + 0.8558 85.58%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Plasma membrane 0.6176 61.76%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8896 88.96%
OATP1B3 inhibitior + 0.9553 95.53%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.7571 75.71%
P-glycoprotein inhibitior - 0.8454 84.54%
P-glycoprotein substrate - 0.9374 93.74%
CYP3A4 substrate - 0.5607 56.07%
CYP2C9 substrate + 0.7980 79.80%
CYP2D6 substrate - 0.7133 71.33%
CYP3A4 inhibition - 0.9459 94.59%
CYP2C9 inhibition - 0.7261 72.61%
CYP2C19 inhibition + 0.5648 56.48%
CYP2D6 inhibition - 0.9005 90.05%
CYP1A2 inhibition + 0.6378 63.78%
CYP2C8 inhibition - 0.7005 70.05%
CYP inhibitory promiscuity + 0.8017 80.17%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Danger 0.4948 49.48%
Eye corrosion + 0.8190 81.90%
Eye irritation + 0.6055 60.55%
Skin irritation + 0.7213 72.13%
Skin corrosion - 0.8173 81.73%
Ames mutagenesis - 0.5570 55.70%
Human Ether-a-go-go-Related Gene inhibition + 0.9004 90.04%
Micronuclear - 0.8600 86.00%
Hepatotoxicity - 0.7038 70.38%
skin sensitisation + 0.5851 58.51%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.5855 58.55%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity - 0.5956 59.56%
Acute Oral Toxicity (c) III 0.7822 78.22%
Estrogen receptor binding + 0.7464 74.64%
Androgen receptor binding - 0.8710 87.10%
Thyroid receptor binding + 0.6641 66.41%
Glucocorticoid receptor binding - 0.5907 59.07%
Aromatase binding + 0.5549 55.49%
PPAR gamma + 0.8803 88.03%
Honey bee toxicity - 0.9514 95.14%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.7880 78.80%

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 96.83% 91.11%
CHEMBL2039 P27338 Monoamine oxidase B 96.09% 92.51%
CHEMBL1951 P21397 Monoamine oxidase A 95.42% 91.49%
CHEMBL221 P23219 Cyclooxygenase-1 92.36% 90.17%
CHEMBL3401 O75469 Pregnane X receptor 89.89% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.87% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.61% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 88.92% 96.00%
CHEMBL230 P35354 Cyclooxygenase-2 85.35% 89.63%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.09% 95.56%
CHEMBL2581 P07339 Cathepsin D 81.96% 98.95%

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.
Elodea canadensis
Persea indica

Cross-Links

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PubChem 101687157
LOTUS LTS0029789
wikiData Q105160547