Avocadienofuran

Details

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Internal ID 07613a2b-ea56-41ad-a0ba-14975b9f64be
Taxonomy Organoheterocyclic compounds > Heteroaromatic compounds
IUPAC Name 2-[(1Z)-trideca-1,12-dienyl]furan
SMILES (Canonical) C=CCCCCCCCCCC=CC1=CC=CO1
SMILES (Isomeric) C=CCCCCCCCCC/C=C\C1=CC=CO1
InChI InChI=1S/C17H26O/c1-2-3-4-5-6-7-8-9-10-11-12-14-17-15-13-16-18-17/h2,12-16H,1,3-11H2/b14-12-
InChI Key MGNABOKOTWYILU-OWBHPGMISA-N
Popularity 0 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 6.80
Atomic LogP (AlogP) 5.99
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 11

Synonyms

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CHEBI:196585
2-[(1Z)-trideca-1,12-dienyl]uran
Q67879707

2D Structure

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2D Structure of Avocadienofuran

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9908 99.08%
Caco-2 + 0.7639 76.39%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Plasma membrane 0.6272 62.72%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9172 91.72%
OATP1B3 inhibitior + 0.9527 95.27%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.7853 78.53%
P-glycoprotein inhibitior - 0.8519 85.19%
P-glycoprotein substrate - 0.9379 93.79%
CYP3A4 substrate - 0.5947 59.47%
CYP2C9 substrate + 0.6107 61.07%
CYP2D6 substrate - 0.6864 68.64%
CYP3A4 inhibition - 0.9550 95.50%
CYP2C9 inhibition - 0.7985 79.85%
CYP2C19 inhibition + 0.5888 58.88%
CYP2D6 inhibition - 0.8939 89.39%
CYP1A2 inhibition + 0.5603 56.03%
CYP2C8 inhibition - 0.7399 73.99%
CYP inhibitory promiscuity + 0.6863 68.63%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7900 79.00%
Carcinogenicity (trinary) Warning 0.3921 39.21%
Eye corrosion + 0.8994 89.94%
Eye irritation + 0.9647 96.47%
Skin irritation + 0.6816 68.16%
Skin corrosion - 0.8552 85.52%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8217 82.17%
Micronuclear - 0.8900 89.00%
Hepatotoxicity - 0.6625 66.25%
skin sensitisation + 0.6329 63.29%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.6077 60.77%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity + 0.4547 45.47%
Acute Oral Toxicity (c) III 0.8398 83.98%
Estrogen receptor binding + 0.6875 68.75%
Androgen receptor binding - 0.7611 76.11%
Thyroid receptor binding + 0.6324 63.24%
Glucocorticoid receptor binding - 0.5268 52.68%
Aromatase binding + 0.5284 52.84%
PPAR gamma + 0.7601 76.01%
Honey bee toxicity - 0.9344 93.44%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.6600 66.00%
Fish aquatic toxicity + 0.8603 86.03%

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 96.47% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 90.73% 91.49%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.87% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 88.59% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.73% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.24% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.89% 93.99%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.87% 96.00%
CHEMBL1781 P11387 DNA topoisomerase I 80.76% 97.00%
CHEMBL1841 P06241 Tyrosine-protein kinase FYN 80.50% 81.29%
CHEMBL3902 P09211 Glutathione S-transferase Pi 80.11% 93.81%

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.
Persea americana

Cross-Links

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PubChem 131751100
LOTUS LTS0185722
wikiData Q67879707