Perillene

Details

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Internal ID fea4c1c0-22b7-4bc8-a30c-47bfc5d7fbc6
Taxonomy Organoheterocyclic compounds > Heteroaromatic compounds
IUPAC Name 3-(4-methylpent-3-enyl)furan
SMILES (Canonical) CC(=CCCC1=COC=C1)C
SMILES (Isomeric) CC(=CCCC1=COC=C1)C
InChI InChI=1S/C10H14O/c1-9(2)4-3-5-10-6-7-11-8-10/h4,6-8H,3,5H2,1-2H3
InChI Key XNGKCOFXDHYSGR-UHFFFAOYSA-N
Popularity 79 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14O
Molecular Weight 150.22 g/mol
Exact Mass 150.104465066 g/mol
Topological Polar Surface Area (TPSA) 13.10 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.18
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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Perillen
539-52-6
3-(4-methylpent-3-en-1-yl)furan
3-(4-Methyl-3-pentenyl)furan
Furan, 3-(4-methyl-3-pentenyl)-
3-(4-methylpent-3-enyl)furan
3-Isohexenylfuran
AM4D4646ZW
UNII-AM4D4646ZW
SCHEMBL310752
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Perillene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9931 99.31%
Caco-2 + 0.9296 92.96%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Nucleus 0.3807 38.07%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7692 76.92%
OATP1B3 inhibitior + 0.9414 94.14%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.8399 83.99%
P-glycoprotein inhibitior - 0.9815 98.15%
P-glycoprotein substrate - 0.9486 94.86%
CYP3A4 substrate - 0.6397 63.97%
CYP2C9 substrate - 0.8037 80.37%
CYP2D6 substrate - 0.6885 68.85%
CYP3A4 inhibition - 0.9619 96.19%
CYP2C9 inhibition - 0.7964 79.64%
CYP2C19 inhibition - 0.6332 63.32%
CYP2D6 inhibition - 0.8701 87.01%
CYP1A2 inhibition - 0.5198 51.98%
CYP2C8 inhibition - 0.8875 88.75%
CYP inhibitory promiscuity + 0.6116 61.16%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7200 72.00%
Carcinogenicity (trinary) Danger 0.4014 40.14%
Eye corrosion + 0.4719 47.19%
Eye irritation + 0.8726 87.26%
Skin irritation + 0.7488 74.88%
Skin corrosion - 0.7477 74.77%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.8300 83.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation + 0.8630 86.30%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity + 0.4625 46.25%
Acute Oral Toxicity (c) III 0.8362 83.62%
Estrogen receptor binding - 0.9112 91.12%
Androgen receptor binding - 0.8017 80.17%
Thyroid receptor binding - 0.8690 86.90%
Glucocorticoid receptor binding - 0.8331 83.31%
Aromatase binding - 0.5926 59.26%
PPAR gamma - 0.8472 84.72%
Honey bee toxicity - 0.9546 95.46%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.5168 51.68%
Fish aquatic toxicity + 0.8606 86.06%

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 91.84% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 91.56% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.13% 94.45%
CHEMBL2581 P07339 Cathepsin D 89.56% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.37% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.83% 99.17%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 80.10% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.05% 96.09%

Cross-Links

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PubChem 68316
NPASS NPC3824
LOTUS LTS0083458
wikiData Q15634089