Brasilamide J

Details

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Internal ID 47fc2b15-82e2-43c5-866b-573e1e95712d
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Secondary alcohols > Cyclohexanols
IUPAC Name [4-[(5Z)-5-(3-amino-2-methyl-3-oxopropylidene)-2-oxofuran-3-yl]-1-hydroxycyclohexyl]methyl acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H23NO6/c1-10(15(18)20)7-13-8-14(16(21)24-13)12-3-5-17(22,6-4-12)9-23-11(2)19/h7-8,10,12,22H,3-6,9H2,1-2H3,(H2,18,20)/b13-7-
InChI Key BMCRLWGEWHAFJC-QPEQYQDCSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C17H23NO6
Molecular Weight 337.40 g/mol
Exact Mass 337.15253745 g/mol
Topological Polar Surface Area (TPSA) 116.00 Ų
XlogP 0.50
Atomic LogP (AlogP) 0.96
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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CHEMBL3581382

2D Structure

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2D Structure of Brasilamide J

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9767 97.67%
Caco-2 - 0.6187 61.87%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.8300 83.00%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8973 89.73%
OATP1B3 inhibitior + 0.9472 94.72%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7864 78.64%
BSEP inhibitior - 0.6864 68.64%
P-glycoprotein inhibitior - 0.7997 79.97%
P-glycoprotein substrate - 0.6933 69.33%
CYP3A4 substrate + 0.5946 59.46%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8909 89.09%
CYP3A4 inhibition - 0.9401 94.01%
CYP2C9 inhibition - 0.8144 81.44%
CYP2C19 inhibition - 0.7892 78.92%
CYP2D6 inhibition - 0.9122 91.22%
CYP1A2 inhibition - 0.8289 82.89%
CYP2C8 inhibition - 0.7264 72.64%
CYP inhibitory promiscuity - 0.8733 87.33%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9028 90.28%
Carcinogenicity (trinary) Non-required 0.6056 60.56%
Eye corrosion - 0.9886 98.86%
Eye irritation - 0.9269 92.69%
Skin irritation - 0.7535 75.35%
Skin corrosion - 0.9347 93.47%
Ames mutagenesis - 0.5070 50.70%
Human Ether-a-go-go-Related Gene inhibition + 0.7097 70.97%
Micronuclear + 0.5600 56.00%
Hepatotoxicity - 0.5549 55.49%
skin sensitisation - 0.8505 85.05%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.8750 87.50%
Nephrotoxicity - 0.6807 68.07%
Acute Oral Toxicity (c) III 0.5790 57.90%
Estrogen receptor binding + 0.8028 80.28%
Androgen receptor binding - 0.5071 50.71%
Thyroid receptor binding + 0.5300 53.00%
Glucocorticoid receptor binding + 0.7439 74.39%
Aromatase binding - 0.6136 61.36%
PPAR gamma - 0.6411 64.11%
Honey bee toxicity - 0.8820 88.20%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 0.8858 88.58%

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 99.10% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.61% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.34% 97.25%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.91% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.30% 97.09%
CHEMBL2581 P07339 Cathepsin D 92.82% 98.95%
CHEMBL299 P17252 Protein kinase C alpha 91.95% 98.03%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.09% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.98% 85.14%
CHEMBL1937 Q92769 Histone deacetylase 2 85.07% 94.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.99% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.83% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.86% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.70% 89.00%
CHEMBL340 P08684 Cytochrome P450 3A4 82.46% 91.19%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 81.76% 82.69%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.64% 100.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.56% 100.00%

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 122178811
LOTUS LTS0115719
wikiData Q104938328