2-(2-Pentenyl)furan

Details

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Internal ID c7731d12-62e6-422d-a9ca-c599443c8fdb
Taxonomy Organoheterocyclic compounds > Heteroaromatic compounds
IUPAC Name 2-[(E)-pent-2-enyl]furan
SMILES (Canonical) CCC=CCC1=CC=CO1
SMILES (Isomeric) CC/C=C/CC1=CC=CO1
InChI InChI=1S/C9H12O/c1-2-3-4-6-9-7-5-8-10-9/h3-5,7-8H,2,6H2,1H3/b4-3+
InChI Key KQMWMXVDLIDHGY-ONEGZZNKSA-N
Popularity 10 references in papers

Physical and Chemical Properties

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Molecular Formula C9H12O
Molecular Weight 136.19 g/mol
Exact Mass 136.088815002 g/mol
Topological Polar Surface Area (TPSA) 13.10 Ų
XlogP 3.30
Atomic LogP (AlogP) 2.79
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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82550-42-3
trans-2-(2-Pentenyl)furan
2-[(E)-pent-2-enyl]furan
2-[(2E)-2-Pentenyl]furan
Furan,2-(2-penten-1-yl)-
(E)-2-(pent-2-en-1-yl)furan
2(trans-2-Pentenyl)furan
(E)-2-(2-Pentenyl)furan
2-(Pent-2(E)-enyl)furan
2-[(E)-2-Pentenyl]furan
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-(2-Pentenyl)furan

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9949 99.49%
Caco-2 + 0.9407 94.07%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Plasma membrane 0.4925 49.25%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8585 85.85%
OATP1B3 inhibitior + 0.9501 95.01%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9138 91.38%
P-glycoprotein inhibitior - 0.9859 98.59%
P-glycoprotein substrate - 0.9457 94.57%
CYP3A4 substrate - 0.7348 73.48%
CYP2C9 substrate - 0.5973 59.73%
CYP2D6 substrate - 0.7023 70.23%
CYP3A4 inhibition - 0.9647 96.47%
CYP2C9 inhibition - 0.7222 72.22%
CYP2C19 inhibition + 0.5592 55.92%
CYP2D6 inhibition - 0.9146 91.46%
CYP1A2 inhibition + 0.6249 62.49%
CYP2C8 inhibition - 0.8994 89.94%
CYP inhibitory promiscuity + 0.7349 73.49%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6300 63.00%
Carcinogenicity (trinary) Danger 0.4638 46.38%
Eye corrosion + 0.7455 74.55%
Eye irritation + 0.9699 96.99%
Skin irritation + 0.7722 77.22%
Skin corrosion - 0.8099 80.99%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4934 49.34%
Micronuclear - 0.7300 73.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation + 0.8243 82.43%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity - 0.5034 50.34%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity - 0.6725 67.25%
Acute Oral Toxicity (c) III 0.8519 85.19%
Estrogen receptor binding - 0.8575 85.75%
Androgen receptor binding - 0.9233 92.33%
Thyroid receptor binding - 0.8785 87.85%
Glucocorticoid receptor binding - 0.7487 74.87%
Aromatase binding - 0.6600 66.00%
PPAR gamma - 0.6635 66.35%
Honey bee toxicity - 0.9731 97.31%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.6515 65.15%

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 90.98% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 87.54% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.95% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.03% 86.33%
CHEMBL2581 P07339 Cathepsin D 83.39% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.58% 95.56%

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.
Nerium oleander

Cross-Links

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PubChem 5369957
NPASS NPC144658