5-bromoagonodepside B

Details

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Internal ID 7dc8ced5-12a2-419f-8f49-d15e246056a6
Taxonomy Phenylpropanoids and polyketides > Depsides and depsidones
IUPAC Name 4-[3-bromo-2-[(E)-but-2-en-2-yl]-4,6-dihydroxy-5-methylbenzoyl]oxy-6-[(E)-but-2-en-2-yl]-2-hydroxy-3-methylbenzoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H25BrO7/c1-7-10(3)14-9-15(12(5)20(26)17(14)23(29)30)32-24(31)18-16(11(4)8-2)19(25)22(28)13(6)21(18)27/h7-9,26-28H,1-6H3,(H,29,30)/b10-7+,11-8+
InChI Key PYZQORWOXDELTM-AMMQDNIMSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C24H25BrO7
Molecular Weight 505.40 g/mol
Exact Mass 504.07837 g/mol
Topological Polar Surface Area (TPSA) 124.00 Ų
XlogP 7.60
Atomic LogP (AlogP) 5.95
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-bromoagonodepside B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9715 97.15%
Caco-2 - 0.6473 64.73%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.8138 81.38%
OATP2B1 inhibitior - 0.5582 55.82%
OATP1B1 inhibitior + 0.8424 84.24%
OATP1B3 inhibitior + 0.8424 84.24%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.9202 92.02%
P-glycoprotein inhibitior - 0.5973 59.73%
P-glycoprotein substrate - 0.8196 81.96%
CYP3A4 substrate - 0.5239 52.39%
CYP2C9 substrate - 0.6050 60.50%
CYP2D6 substrate - 0.9005 90.05%
CYP3A4 inhibition - 0.7847 78.47%
CYP2C9 inhibition + 0.7796 77.96%
CYP2C19 inhibition + 0.5647 56.47%
CYP2D6 inhibition - 0.8685 86.85%
CYP1A2 inhibition + 0.6602 66.02%
CYP2C8 inhibition + 0.6237 62.37%
CYP inhibitory promiscuity + 0.7220 72.20%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.6736 67.36%
Carcinogenicity (trinary) Danger 0.6286 62.86%
Eye corrosion - 0.9891 98.91%
Eye irritation - 0.6222 62.22%
Skin irritation - 0.7586 75.86%
Skin corrosion - 0.9554 95.54%
Ames mutagenesis - 0.5778 57.78%
Human Ether-a-go-go-Related Gene inhibition - 0.4788 47.88%
Micronuclear + 0.7074 70.74%
Hepatotoxicity + 0.7160 71.60%
skin sensitisation - 0.6721 67.21%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity - 0.6412 64.12%
Acute Oral Toxicity (c) III 0.5505 55.05%
Estrogen receptor binding + 0.8834 88.34%
Androgen receptor binding + 0.6318 63.18%
Thyroid receptor binding - 0.4936 49.36%
Glucocorticoid receptor binding + 0.5945 59.45%
Aromatase binding + 0.5341 53.41%
PPAR gamma + 0.7518 75.18%
Honey bee toxicity - 0.8053 80.53%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 95.85% 93.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 92.28% 95.50%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 92.09% 97.21%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 91.84% 94.42%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.15% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 86.82% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.47% 94.00%
CHEMBL2581 P07339 Cathepsin D 86.45% 98.95%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 86.37% 83.57%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 85.26% 89.34%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.32% 99.17%
CHEMBL3194 P02766 Transthyretin 84.30% 90.71%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.71% 96.09%
CHEMBL5905 Q04828 Aldo-keto reductase family 1 member C1 82.80% 91.79%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 82.69% 87.67%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 82.07% 81.11%
CHEMBL2535 P11166 Glucose transporter 82.03% 98.75%
CHEMBL3714130 P46095 G-protein coupled receptor 6 82.02% 97.36%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.87% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.51% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.23% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.07% 95.89%
CHEMBL5847 P52895 Aldo-keto reductase family 1 member C2 80.90% 92.50%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.55% 96.95%

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 146684026
LOTUS LTS0267288
wikiData Q105216887