2-(12-Tridecyn-1-yl)furan

Details

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Internal ID 8be09207-d085-45d4-b723-b1552b54a6b6
Taxonomy Organoheterocyclic compounds > Heteroaromatic compounds
IUPAC Name 2-tridec-12-ynylfuran
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H26O/c1-2-3-4-5-6-7-8-9-10-11-12-14-17-15-13-16-18-17/h1,13,15-16H,3-12,14H2
InChI Key ONYOTXAYIZRIPJ-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C17H26O
Molecular Weight 246.40 g/mol
Exact Mass 246.198365449 g/mol
Topological Polar Surface Area (TPSA) 13.10 Ų
XlogP 6.50
Atomic LogP (AlogP) 5.36
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 11

Synonyms

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2-(12-Tridecyn-1-yl)furan
SDCCGMLS-0066920.P001
2-tridec-12-ynyluran
2-(trideca-12-ynyl)furan
SPECTRUM1505808
SCHEMBL8158965
2-(tridec-12-yn-1-yl)furan
CHEMBL1453347
CHEBI:177734
DTXSID001312032
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2-(12-Tridecyn-1-yl)furan

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9895 98.95%
Caco-2 + 0.8368 83.68%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.4014 40.14%
OATP2B1 inhibitior - 0.8570 85.70%
OATP1B1 inhibitior + 0.9216 92.16%
OATP1B3 inhibitior + 0.9572 95.72%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.7121 71.21%
P-glycoprotein inhibitior - 0.9268 92.68%
P-glycoprotein substrate - 0.9405 94.05%
CYP3A4 substrate - 0.5986 59.86%
CYP2C9 substrate - 0.7928 79.28%
CYP2D6 substrate - 0.6576 65.76%
CYP3A4 inhibition - 0.9432 94.32%
CYP2C9 inhibition - 0.6760 67.60%
CYP2C19 inhibition + 0.5588 55.88%
CYP2D6 inhibition - 0.9056 90.56%
CYP1A2 inhibition + 0.5360 53.60%
CYP2C8 inhibition - 0.7155 71.55%
CYP inhibitory promiscuity + 0.5901 59.01%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Danger 0.4111 41.11%
Eye corrosion + 0.8361 83.61%
Eye irritation + 0.5699 56.99%
Skin irritation + 0.7772 77.72%
Skin corrosion - 0.5869 58.69%
Ames mutagenesis - 0.5870 58.70%
Human Ether-a-go-go-Related Gene inhibition + 0.8652 86.52%
Micronuclear - 0.8500 85.00%
Hepatotoxicity - 0.5663 56.63%
skin sensitisation - 0.5746 57.46%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.6077 60.77%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity + 0.5776 57.76%
Acute Oral Toxicity (c) III 0.6688 66.88%
Estrogen receptor binding + 0.6403 64.03%
Androgen receptor binding - 0.8647 86.47%
Thyroid receptor binding + 0.6330 63.30%
Glucocorticoid receptor binding - 0.4789 47.89%
Aromatase binding - 0.5834 58.34%
PPAR gamma + 0.8249 82.49%
Honey bee toxicity - 0.9520 95.20%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity + 0.5721 57.21%
Fish aquatic toxicity - 0.6188 61.88%

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 97.13% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 88.56% 91.49%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.79% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 87.12% 94.73%
CHEMBL2581 P07339 Cathepsin D 84.16% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 81.46% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.37% 96.09%

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 americana

Cross-Links

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PubChem 6857797
LOTUS LTS0054204
wikiData Q67879708