3-((1R)-1-Hydroxybutyl)-4-bromo-5-(bromomethylene)furan-2-one

Details

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Internal ID 16eef688-5fd9-44f5-9305-05960b79785e
Taxonomy Organoheterocyclic compounds > Dihydrofurans > Furanones > Butenolides
IUPAC Name (5Z)-4-bromo-5-(bromomethylidene)-3-[(1R)-1-hydroxybutyl]furan-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H10Br2O3/c1-2-3-5(12)7-8(11)6(4-10)14-9(7)13/h4-5,12H,2-3H2,1H3/b6-4-/t5-/m1/s1
InChI Key GWLDADMCKOCKLF-WEWOIACBSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C9H10Br2O3
Molecular Weight 325.98 g/mol
Exact Mass 325.89762 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.59
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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SCHEMBL13599559
3-((1R)-1-Hydroxybutyl)-4-bromo-5-(bromomethylene)furan-2-one
(5z)-4-bromo-5-(bromomethylene)-3 [(1r)-1-hydroxybutyl]furan-2(5h)-one
(5Z)-4-bromo-5-(bromomethylene)-3-[(1R)-1-hydroxybutyl]furan-2-one

2D Structure

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2D Structure of 3-((1R)-1-Hydroxybutyl)-4-bromo-5-(bromomethylene)furan-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9951 99.51%
Caco-2 + 0.7853 78.53%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.5894 58.94%
OATP2B1 inhibitior - 0.8532 85.32%
OATP1B1 inhibitior + 0.9007 90.07%
OATP1B3 inhibitior + 0.9505 95.05%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.7570 75.70%
BSEP inhibitior - 0.9064 90.64%
P-glycoprotein inhibitior - 0.9561 95.61%
P-glycoprotein substrate - 0.9528 95.28%
CYP3A4 substrate - 0.5921 59.21%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8454 84.54%
CYP3A4 inhibition - 0.8191 81.91%
CYP2C9 inhibition - 0.7565 75.65%
CYP2C19 inhibition - 0.7036 70.36%
CYP2D6 inhibition - 0.9134 91.34%
CYP1A2 inhibition - 0.8517 85.17%
CYP2C8 inhibition - 0.9481 94.81%
CYP inhibitory promiscuity - 0.7952 79.52%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8589 85.89%
Carcinogenicity (trinary) Danger 0.4601 46.01%
Eye corrosion - 0.9262 92.62%
Eye irritation + 0.7151 71.51%
Skin irritation - 0.5745 57.45%
Skin corrosion - 0.8230 82.30%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6021 60.21%
Micronuclear - 0.8452 84.52%
Hepatotoxicity - 0.6375 63.75%
skin sensitisation - 0.7121 71.21%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity + 0.5293 52.93%
Acute Oral Toxicity (c) III 0.6242 62.42%
Estrogen receptor binding + 0.5832 58.32%
Androgen receptor binding - 0.6542 65.42%
Thyroid receptor binding + 0.5251 52.51%
Glucocorticoid receptor binding - 0.4671 46.71%
Aromatase binding - 0.8590 85.90%
PPAR gamma - 0.5799 57.99%
Honey bee toxicity - 0.9263 92.63%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.8865 88.65%

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 96.04% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.86% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.76% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 87.49% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.26% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 84.64% 94.73%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.19% 97.25%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.81% 99.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.40% 99.17%

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.
Cordia fragrantissima
Cordia globifera
Cordia millenii

Cross-Links

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PubChem 6475696
LOTUS LTS0004782
wikiData Q105148471