4-Bromo-3-butyl-5-(dibromomethyl)-5-hydroxy-2(5h)-furanone

Details

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Internal ID 037668e0-35a7-4b8e-9e44-aff35ab6e224
Taxonomy Organoheterocyclic compounds > Dihydrofurans > Furanones > Butenolides
IUPAC Name 4-bromo-3-butyl-5-(dibromomethyl)-5-hydroxyfuran-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H11Br3O3/c1-2-3-4-5-6(10)9(14,8(11)12)15-7(5)13/h8,14H,2-4H2,1H3
InChI Key JCYSHOZCQQQZIK-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C9H11Br3O3
Molecular Weight 406.89 g/mol
Exact Mass 405.82378 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.19
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-Bromo-3-butyl-5-(dibromomethyl)-5-hydroxy-2(5h)-furanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9862 98.62%
Caco-2 + 0.7871 78.71%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.5510 55.10%
OATP2B1 inhibitior - 0.8517 85.17%
OATP1B1 inhibitior + 0.8819 88.19%
OATP1B3 inhibitior + 0.9478 94.78%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.9393 93.93%
P-glycoprotein inhibitior - 0.9449 94.49%
P-glycoprotein substrate - 0.8773 87.73%
CYP3A4 substrate - 0.5389 53.89%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8588 85.88%
CYP3A4 inhibition - 0.7192 71.92%
CYP2C9 inhibition - 0.6046 60.46%
CYP2C19 inhibition - 0.6003 60.03%
CYP2D6 inhibition - 0.8679 86.79%
CYP1A2 inhibition - 0.6878 68.78%
CYP2C8 inhibition - 0.8934 89.34%
CYP inhibitory promiscuity - 0.5569 55.69%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8308 83.08%
Carcinogenicity (trinary) Danger 0.4657 46.57%
Eye corrosion - 0.9041 90.41%
Eye irritation - 0.5983 59.83%
Skin irritation - 0.5212 52.12%
Skin corrosion - 0.7941 79.41%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6505 65.05%
Micronuclear - 0.8526 85.26%
Hepatotoxicity + 0.6425 64.25%
skin sensitisation - 0.6653 66.53%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity + 0.5886 58.86%
Acute Oral Toxicity (c) III 0.6709 67.09%
Estrogen receptor binding - 0.6822 68.22%
Androgen receptor binding - 0.6586 65.86%
Thyroid receptor binding - 0.4919 49.19%
Glucocorticoid receptor binding - 0.5672 56.72%
Aromatase binding - 0.8563 85.63%
PPAR gamma - 0.5475 54.75%
Honey bee toxicity - 0.9646 96.46%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.9784 97.84%

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 98.03% 98.95%
CHEMBL299 P17252 Protein kinase C alpha 96.03% 98.03%
CHEMBL230 P35354 Cyclooxygenase-2 95.25% 89.63%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.05% 97.25%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 90.53% 85.94%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.42% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.29% 95.56%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 87.20% 95.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.93% 91.11%
CHEMBL218 P21554 Cannabinoid CB1 receptor 85.43% 96.61%
CHEMBL221 P23219 Cyclooxygenase-1 84.02% 90.17%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.50% 93.56%
CHEMBL3401 O75469 Pregnane X receptor 81.17% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.97% 86.33%

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 14017701
LOTUS LTS0258403
wikiData Q105125267