5-Bromoochrephilone

Details

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Internal ID 73e1b62a-8d50-4652-a6bf-763d598e1f0d
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones > Cyclohexenones
IUPAC Name (6aR,9R,9aR)-9-acetyl-5-bromo-3-[(1E,3E,5S)-3,5-dimethylhepta-1,3-dienyl]-6a-methyl-9,9a-dihydrofuro[2,3-h]isochromene-6,8-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H25BrO5/c1-6-12(2)9-13(3)7-8-15-10-16-17(11-28-15)19-18(14(4)25)22(27)29-23(19,5)21(26)20(16)24/h7-12,18-19H,6H2,1-5H3/b8-7+,13-9+/t12-,18-,19-,23+/m0/s1
InChI Key YVLXPVGJCIVWMQ-WJKJBVSTSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C23H25BrO5
Molecular Weight 461.30 g/mol
Exact Mass 460.08854 g/mol
Topological Polar Surface Area (TPSA) 69.70 Ų
XlogP 4.40
Atomic LogP (AlogP) 4.70
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-Bromoochrephilone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9926 99.26%
Caco-2 + 0.5302 53.02%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.4346 43.46%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7737 77.37%
OATP1B3 inhibitior + 0.9271 92.71%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9448 94.48%
P-glycoprotein inhibitior + 0.6860 68.60%
P-glycoprotein substrate - 0.6253 62.53%
CYP3A4 substrate + 0.6464 64.64%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8910 89.10%
CYP3A4 inhibition - 0.5911 59.11%
CYP2C9 inhibition - 0.6026 60.26%
CYP2C19 inhibition - 0.7228 72.28%
CYP2D6 inhibition - 0.9183 91.83%
CYP1A2 inhibition - 0.7560 75.60%
CYP2C8 inhibition + 0.5468 54.68%
CYP inhibitory promiscuity + 0.5814 58.14%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9429 94.29%
Carcinogenicity (trinary) Danger 0.6268 62.68%
Eye corrosion - 0.9744 97.44%
Eye irritation - 0.9501 95.01%
Skin irritation - 0.6061 60.61%
Skin corrosion - 0.8906 89.06%
Ames mutagenesis - 0.5054 50.54%
Human Ether-a-go-go-Related Gene inhibition + 0.8077 80.77%
Micronuclear - 0.5400 54.00%
Hepatotoxicity + 0.6032 60.32%
skin sensitisation - 0.7231 72.31%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.4863 48.63%
Acute Oral Toxicity (c) III 0.5881 58.81%
Estrogen receptor binding + 0.8066 80.66%
Androgen receptor binding + 0.6800 68.00%
Thyroid receptor binding + 0.6362 63.62%
Glucocorticoid receptor binding + 0.7281 72.81%
Aromatase binding - 0.5089 50.89%
PPAR gamma + 0.6205 62.05%
Honey bee toxicity - 0.8396 83.96%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9933 99.33%

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 96.08% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.63% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.54% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.16% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.94% 97.25%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.57% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 92.57% 94.73%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 90.89% 85.30%
CHEMBL1937 Q92769 Histone deacetylase 2 90.50% 94.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.48% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.30% 95.56%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 86.05% 89.67%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 85.84% 94.80%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.85% 93.99%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.75% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.70% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.66% 99.23%
CHEMBL255 P29275 Adenosine A2b receptor 81.34% 98.59%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.69% 97.09%
CHEMBL5103 Q969S8 Histone deacetylase 10 80.03% 90.08%

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 10049934
LOTUS LTS0105507
wikiData Q75058488