Xanthomonasin B

Details

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Internal ID a73eb993-2667-4581-997e-62fa3f7a8eb5
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Annonaceous acetogenins
IUPAC Name (5R,5aS)-2,5-dihydroxy-5a-methyl-8-octanoyl-7-oxo-5-[(E)-prop-1-enyl]-4H-furo[2,3-e][1]benzofuran-3-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H28O7/c1-4-6-7-8-9-10-16(25)17-18-19-14(15(13-24)20(26)29-19)12-23(28,11-5-2)22(18,3)30-21(17)27/h5,11,13,26,28H,4,6-10,12H2,1-3H3/b11-5+/t22-,23-/m0/s1
InChI Key NHVGGOQRKIKXEW-FCYCGOIYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C23H28O7
Molecular Weight 416.50 g/mol
Exact Mass 416.18350323 g/mol
Topological Polar Surface Area (TPSA) 114.00 Ų
XlogP 3.70
Atomic LogP (AlogP) 3.66
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Xanthomonasin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9910 99.10%
Caco-2 - 0.5923 59.23%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.8118 81.18%
OATP2B1 inhibitior - 0.7128 71.28%
OATP1B1 inhibitior + 0.7820 78.20%
OATP1B3 inhibitior + 0.9453 94.53%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.7752 77.52%
P-glycoprotein inhibitior - 0.4425 44.25%
P-glycoprotein substrate + 0.5182 51.82%
CYP3A4 substrate + 0.6519 65.19%
CYP2C9 substrate + 0.6120 61.20%
CYP2D6 substrate - 0.8781 87.81%
CYP3A4 inhibition + 0.7691 76.91%
CYP2C9 inhibition - 0.7478 74.78%
CYP2C19 inhibition - 0.7386 73.86%
CYP2D6 inhibition - 0.9181 91.81%
CYP1A2 inhibition + 0.5447 54.47%
CYP2C8 inhibition + 0.5921 59.21%
CYP inhibitory promiscuity - 0.7789 77.89%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Danger 0.5215 52.15%
Eye corrosion - 0.9912 99.12%
Eye irritation - 0.8426 84.26%
Skin irritation + 0.5642 56.42%
Skin corrosion - 0.9141 91.41%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4924 49.24%
Micronuclear - 0.7300 73.00%
Hepatotoxicity - 0.5176 51.76%
skin sensitisation - 0.8265 82.65%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity + 0.6291 62.91%
Acute Oral Toxicity (c) II 0.3613 36.13%
Estrogen receptor binding + 0.8474 84.74%
Androgen receptor binding + 0.6717 67.17%
Thyroid receptor binding - 0.4873 48.73%
Glucocorticoid receptor binding + 0.8431 84.31%
Aromatase binding + 0.7612 76.12%
PPAR gamma + 0.8069 80.69%
Honey bee toxicity - 0.9117 91.17%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.7324 73.24%
Fish aquatic toxicity + 0.9971 99.71%

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
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 99.01% 95.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.75% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.41% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 95.97% 89.63%
CHEMBL299 P17252 Protein kinase C alpha 94.68% 98.03%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.61% 95.56%
CHEMBL221 P23219 Cyclooxygenase-1 93.57% 90.17%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 92.23% 98.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.24% 96.09%
CHEMBL2996 Q05655 Protein kinase C delta 91.02% 97.79%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 87.42% 96.77%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.10% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.26% 99.23%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 84.54% 91.81%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.34% 97.25%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.11% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.03% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 80.05% 94.73%
CHEMBL340 P08684 Cytochrome P450 3A4 80.00% 91.19%

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 136798818
LOTUS LTS0013233
wikiData Q77572909