Furan, 2-(1-cyclopenten-1-yl)-

Details

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Internal ID c255c9e2-f2ab-466b-9d4b-79f8e814dd8e
Taxonomy Organoheterocyclic compounds > Heteroaromatic compounds
IUPAC Name 2-(cyclopenten-1-yl)furan
SMILES (Canonical) C1CC=C(C1)C2=CC=CO2
SMILES (Isomeric) C1CC=C(C1)C2=CC=CO2
InChI InChI=1S/C9H10O/c1-2-5-8(4-1)9-6-3-7-10-9/h3-4,6-7H,1-2,5H2
InChI Key LDQSHVHRBJJNDT-UHFFFAOYSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C9H10O
Molecular Weight 134.17 g/mol
Exact Mass 134.073164938 g/mol
Topological Polar Surface Area (TPSA) 13.10 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.85
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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115754-78-4
2-(1-Cyclopentenyl)furan
2-(CYCLOPENT-1-EN-1-YL)FURAN
2-(cyclopenten-1-yl)furan
2-(1-cyclopentenyl)-furan
DTXSID70342767
LDQSHVHRBJJNDT-UHFFFAOYSA-N
2-(1-Cyclopenten-1-yl)furan #

2D Structure

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2D Structure of Furan, 2-(1-cyclopenten-1-yl)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9936 99.36%
Caco-2 + 0.9599 95.99%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Plasma membrane 0.4046 40.46%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9655 96.55%
OATP1B3 inhibitior + 0.9547 95.47%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.9238 92.38%
P-glycoprotein inhibitior - 0.9813 98.13%
P-glycoprotein substrate - 0.9785 97.85%
CYP3A4 substrate - 0.6970 69.70%
CYP2C9 substrate - 0.6147 61.47%
CYP2D6 substrate - 0.6790 67.90%
CYP3A4 inhibition - 0.9488 94.88%
CYP2C9 inhibition - 0.8275 82.75%
CYP2C19 inhibition - 0.5714 57.14%
CYP2D6 inhibition - 0.9194 91.94%
CYP1A2 inhibition + 0.6537 65.37%
CYP2C8 inhibition - 0.8620 86.20%
CYP inhibitory promiscuity + 0.8618 86.18%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7900 79.00%
Carcinogenicity (trinary) Warning 0.4017 40.17%
Eye corrosion + 0.7003 70.03%
Eye irritation + 0.9959 99.59%
Skin irritation + 0.6430 64.30%
Skin corrosion - 0.9100 91.00%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5679 56.79%
Micronuclear - 0.8300 83.00%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation + 0.5346 53.46%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.5743 57.43%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity - 0.5640 56.40%
Acute Oral Toxicity (c) III 0.8313 83.13%
Estrogen receptor binding - 0.8494 84.94%
Androgen receptor binding - 0.7441 74.41%
Thyroid receptor binding - 0.9069 90.69%
Glucocorticoid receptor binding - 0.7832 78.32%
Aromatase binding - 0.6870 68.70%
PPAR gamma - 0.8743 87.43%
Honey bee toxicity - 0.9406 94.06%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.7330 73.30%

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 91.54% 91.11%
CHEMBL3192 Q9BY41 Histone deacetylase 8 88.61% 93.99%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.91% 95.56%
CHEMBL4208 P20618 Proteasome component C5 83.47% 90.00%
CHEMBL2954 P25774 Cathepsin S 83.12% 95.60%
CHEMBL3401 O75469 Pregnane X receptor 82.06% 94.73%

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.
Illicium verum

Cross-Links

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PubChem 584283
NPASS NPC105033
LOTUS LTS0109725
wikiData Q104948949