Xestodecalactone E

Details

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Internal ID c98816f2-bf76-47c9-9308-0b2a9d7e5939
Taxonomy Organoheterocyclic compounds > Oxocins
IUPAC Name (4S,6R)-6-butoxy-9,11-dihydroxy-10-methoxy-4-methyl-4,5,6,7-tetrahydro-1H-3-benzoxecine-2,8-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H26O7/c1-4-5-6-25-13-7-11(2)26-16(22)9-12-8-15(21)19(24-3)18(23)17(12)14(20)10-13/h8,11,13,21,23H,4-7,9-10H2,1-3H3/t11-,13+/m0/s1
InChI Key ZXGUFOGUSHSYOJ-WCQYABFASA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C19H26O7
Molecular Weight 366.40 g/mol
Exact Mass 366.16785316 g/mol
Topological Polar Surface Area (TPSA) 102.00 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.74
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Xestodecalactone E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8843 88.43%
Caco-2 + 0.7264 72.64%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7676 76.76%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7904 79.04%
OATP1B3 inhibitior + 0.8393 83.93%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.4510 45.10%
P-glycoprotein inhibitior - 0.6695 66.95%
P-glycoprotein substrate - 0.6307 63.07%
CYP3A4 substrate + 0.6020 60.20%
CYP2C9 substrate + 0.8166 81.66%
CYP2D6 substrate - 0.8391 83.91%
CYP3A4 inhibition + 0.6287 62.87%
CYP2C9 inhibition - 0.8359 83.59%
CYP2C19 inhibition - 0.5401 54.01%
CYP2D6 inhibition - 0.9274 92.74%
CYP1A2 inhibition + 0.5911 59.11%
CYP2C8 inhibition + 0.5365 53.65%
CYP inhibitory promiscuity - 0.8280 82.80%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.7393 73.93%
Eye corrosion - 0.9902 99.02%
Eye irritation - 0.7030 70.30%
Skin irritation - 0.8289 82.89%
Skin corrosion - 0.9648 96.48%
Ames mutagenesis - 0.6154 61.54%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.8800 88.00%
Hepatotoxicity - 0.5215 52.15%
skin sensitisation - 0.7997 79.97%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.6689 66.89%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.8179 81.79%
Acute Oral Toxicity (c) III 0.4518 45.18%
Estrogen receptor binding + 0.7059 70.59%
Androgen receptor binding + 0.6004 60.04%
Thyroid receptor binding + 0.5181 51.81%
Glucocorticoid receptor binding + 0.7967 79.67%
Aromatase binding - 0.5084 50.84%
PPAR gamma + 0.7343 73.43%
Honey bee toxicity - 0.8801 88.01%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.9823 98.23%

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 99.71% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.34% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.85% 99.17%
CHEMBL2581 P07339 Cathepsin D 95.44% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 93.96% 91.49%
CHEMBL217 P14416 Dopamine D2 receptor 92.32% 95.62%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.16% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.70% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.83% 86.33%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 87.02% 90.71%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.79% 92.94%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.03% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.50% 95.56%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 84.49% 82.38%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.89% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.79% 89.00%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 83.40% 96.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.83% 99.23%
CHEMBL1907 P15144 Aminopeptidase N 81.76% 93.31%
CHEMBL2535 P11166 Glucose transporter 80.82% 98.75%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.81% 95.89%

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 60154236
LOTUS LTS0220567
wikiData Q77375757