Acetoxyfimbrolide

Details

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Internal ID 8be22571-3130-4b1a-9e70-4fa64f1a08a5
Taxonomy Organoheterocyclic compounds > Dihydrofurans > Furanones > Butenolides
IUPAC Name [(1R)-1-[(5E)-4-bromo-5-(bromomethylidene)-2-oxofuran-3-yl]butyl] acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H12Br2O4/c1-3-4-7(16-6(2)14)9-10(13)8(5-12)17-11(9)15/h5,7H,3-4H2,1-2H3/b8-5+/t7-/m1/s1
InChI Key ZHKRZTOJPXQAJI-KBUNYLKBSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C11H12Br2O4
Molecular Weight 368.02 g/mol
Exact Mass 367.90818 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 2.60
Atomic LogP (AlogP) 3.16
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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((1R)-1-((5E)-4-bromo-5-(bromomethylidene)-2-oxofuran-3-yl)butyl) acetate
[(1R)-1-[(5E)-4-bromo-5-(bromomethylidene)-2-oxofuran-3-yl]butyl] acetate
RefChem:109032
CHEMBL498428

2D Structure

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2D Structure of Acetoxyfimbrolide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9863 98.63%
Caco-2 + 0.6451 64.51%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.5427 54.27%
OATP2B1 inhibitior - 0.8505 85.05%
OATP1B1 inhibitior + 0.8963 89.63%
OATP1B3 inhibitior + 0.9357 93.57%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.8788 87.88%
P-glycoprotein inhibitior - 0.9222 92.22%
P-glycoprotein substrate - 0.9222 92.22%
CYP3A4 substrate - 0.5099 50.99%
CYP2C9 substrate + 0.6068 60.68%
CYP2D6 substrate - 0.8807 88.07%
CYP3A4 inhibition - 0.7082 70.82%
CYP2C9 inhibition - 0.6711 67.11%
CYP2C19 inhibition - 0.5503 55.03%
CYP2D6 inhibition - 0.8976 89.76%
CYP1A2 inhibition - 0.7030 70.30%
CYP2C8 inhibition - 0.8786 87.86%
CYP inhibitory promiscuity - 0.5449 54.49%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8690 86.90%
Carcinogenicity (trinary) Non-required 0.4169 41.69%
Eye corrosion - 0.9287 92.87%
Eye irritation + 0.7967 79.67%
Skin irritation - 0.6557 65.57%
Skin corrosion - 0.8774 87.74%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6256 62.56%
Micronuclear - 0.7926 79.26%
Hepatotoxicity - 0.5343 53.43%
skin sensitisation - 0.7768 77.68%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity - 0.5889 58.89%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity + 0.7205 72.05%
Acute Oral Toxicity (c) III 0.6274 62.74%
Estrogen receptor binding + 0.6202 62.02%
Androgen receptor binding - 0.4874 48.74%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding - 0.5149 51.49%
Aromatase binding - 0.7212 72.12%
PPAR gamma + 0.5410 54.10%
Honey bee toxicity - 0.8975 89.75%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5383 53.83%
Fish aquatic toxicity + 0.9785 97.85%

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
CHEMBL2581 P07339 Cathepsin D 96.56% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.31% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.10% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 88.91% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.18% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.03% 94.45%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.70% 95.50%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.17% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.87% 99.23%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.91% 93.56%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.87% 95.56%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 10090405
LOTUS LTS0104887
wikiData Q105375816