2-Pentylfuran

Details

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Internal ID a18b5ed7-07f3-4bca-84ca-72d3cb025cd2
Taxonomy Organoheterocyclic compounds > Heteroaromatic compounds
IUPAC Name 2-pentylfuran
SMILES (Canonical) CCCCCC1=CC=CO1
SMILES (Isomeric) CCCCCC1=CC=CO1
InChI InChI=1S/C9H14O/c1-2-3-4-6-9-7-5-8-10-9/h5,7-8H,2-4,6H2,1H3
InChI Key YVBAUDVGOFCUSG-UHFFFAOYSA-N
Popularity 698 references in papers

Physical and Chemical Properties

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Molecular Formula C9H14O
Molecular Weight 138.21 g/mol
Exact Mass 138.104465066 g/mol
Topological Polar Surface Area (TPSA) 13.10 Ų
XlogP 3.70
Atomic LogP (AlogP) 3.01
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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3777-69-3
2-Amylfuran
2-n-Pentylfuran
Furan, 2-pentyl-
Furan, pentyl-
PENTYLFURAN
FEMA No. 3317
2-Pentylfuran (natural)
2-pentyl furan
EINECS 223-234-7
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-Pentylfuran

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9947 99.47%
Caco-2 + 0.9701 97.01%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Plasma membrane 0.4024 40.24%
OATP2B1 inhibitior - 0.8576 85.76%
OATP1B1 inhibitior + 0.8923 89.23%
OATP1B3 inhibitior + 0.9515 95.15%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9443 94.43%
P-glycoprotein inhibitior - 0.9908 99.08%
P-glycoprotein substrate - 0.8657 86.57%
CYP3A4 substrate - 0.6778 67.78%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.6668 66.68%
CYP3A4 inhibition - 0.9577 95.77%
CYP2C9 inhibition - 0.8096 80.96%
CYP2C19 inhibition - 0.5377 53.77%
CYP2D6 inhibition - 0.8935 89.35%
CYP1A2 inhibition + 0.6458 64.58%
CYP2C8 inhibition - 0.7852 78.52%
CYP inhibitory promiscuity - 0.5567 55.67%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Warning 0.3731 37.31%
Eye corrosion + 0.7497 74.97%
Eye irritation + 0.9628 96.28%
Skin irritation + 0.8526 85.26%
Skin corrosion - 0.8898 88.98%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5071 50.71%
Micronuclear - 0.9200 92.00%
Hepatotoxicity - 0.5026 50.26%
skin sensitisation + 0.5652 56.52%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.5566 55.66%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity + 0.6027 60.27%
Acute Oral Toxicity (c) III 0.7431 74.31%
Estrogen receptor binding - 0.8670 86.70%
Androgen receptor binding - 0.8218 82.18%
Thyroid receptor binding - 0.8695 86.95%
Glucocorticoid receptor binding - 0.6532 65.32%
Aromatase binding - 0.7203 72.03%
PPAR gamma - 0.6580 65.80%
Honey bee toxicity - 0.9933 99.33%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.7150 71.50%
Fish aquatic toxicity + 0.7160 71.60%

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 95.35% 89.76%
CHEMBL2581 P07339 Cathepsin D 94.27% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 93.14% 92.08%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.73% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 89.93% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.07% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.91% 96.09%
CHEMBL1907 P15144 Aminopeptidase N 82.82% 93.31%
CHEMBL230 P35354 Cyclooxygenase-2 82.53% 89.63%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 82.36% 93.65%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.19% 99.17%

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.
Achillea grandifolia
Actaea cimicifuga
Actaea dahurica
Actaea simplex
Akebia quinata
Akebia trifoliata
Allium ampeloprasum
Allium cepa
Angelica acutiloba
Angelica gigas
Angelica sinensis
Arachis hypogaea
Arnebia euchroma
Arnebia guttata
Aspalathus linearis
Astragalus trimestris
Bupleurum chinense
Bupleurum falcatum
Bupleurum scorzonerifolium
Cannabis sativa
Capsella bursa-pastoris
Capsicum annuum
Chrysopogon zizanioides
Citrullus lanatus
Citrus × aurantium
Conioselinum anthriscoides
Crocus sativus
Daphne odora
Dendrobium chrysanthum
Eleutherococcus giraldii
Gardenia jasminoides
Geum heterocarpum
Glycyrrhiza
Glycyrrhiza glabra
Gossypium herbaceum
Hansenia forbesii
Hansenia weberbaueriana
Helianthus tuberosus
Hyptis spicigera
Inula helenium
Leonotis leonurus
Ligusticum officinale
Ligusticum striatum
Lithospermum erythrorhizon
Lobelia chinensis
Lonicera japonica
Lycium barbarum
Lycium chinense
Nelumbo nucifera
Nepeta racemosa
Oplopanax elatus
Origanum vulgare
Panax ginseng
Patrinia scabiosifolia
Patrinia villosa
Phaseolus vulgaris
Pinellia ternata
Pistacia vera
Polygala senega
Polygonatum odoratum
Portulaca oleracea
Prunus dulcis
Prunus persica
Pyrus pyrifolia
Scleromitrion diffusum
Scutellaria baicalensis
Scutellaria barbata
Senna alexandrina
Sideritis dichotoma
Sideritis hispida
Stevia rebaudiana
Tripleurospermum inodorum
Typha angustifolia
Vitis rotundifolia
Zea mays

Cross-Links

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PubChem 19602
NPASS NPC42471
LOTUS LTS0044471
wikiData Q27161382