Euphorbialoid E

Details

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Internal ID c4966bb8-2940-48d6-bc2c-69e9fbded154
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Pentacarboxylic acids and derivatives
IUPAC Name [(1S,2R,3R,4S,5S,7R,8S,9R,10R,11S)-2,7,8-triacetyloxy-11-(2-acetyloxypropan-2-yl)-5,9-dimethyl-14-oxo-16-oxatetracyclo[7.5.2.01,10.03,7]hexadec-12-en-4-yl] pyridine-3-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C34H41NO12/c1-17-14-34(47-21(5)39)25(26(17)45-29(41)22-10-9-13-35-15-22)28(43-18(2)36)33-16-42-32(8,30(34)44-19(3)37)27(33)23(11-12-24(33)40)31(6,7)46-20(4)38/h9-13,15,17,23,25-28,30H,14,16H2,1-8H3/t17-,23-,25+,26-,27-,28+,30-,32+,33+,34+/m0/s1
InChI Key XUEVAXNOCWUQGK-QQFHXDICSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C34H41NO12
Molecular Weight 655.70 g/mol
Exact Mass 655.26287574 g/mol
Topological Polar Surface Area (TPSA) 171.00 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.93
H-Bond Acceptor 13
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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CHEMBL2030583

2D Structure

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2D Structure of Euphorbialoid E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9823 98.23%
Caco-2 - 0.7777 77.77%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.6233 62.33%
OATP2B1 inhibitior - 0.8577 85.77%
OATP1B1 inhibitior + 0.8551 85.51%
OATP1B3 inhibitior + 0.8327 83.27%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.9964 99.64%
P-glycoprotein inhibitior + 0.9193 91.93%
P-glycoprotein substrate + 0.6390 63.90%
CYP3A4 substrate + 0.6906 69.06%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8959 89.59%
CYP3A4 inhibition + 0.5656 56.56%
CYP2C9 inhibition - 0.8001 80.01%
CYP2C19 inhibition - 0.6636 66.36%
CYP2D6 inhibition - 0.9127 91.27%
CYP1A2 inhibition - 0.6079 60.79%
CYP2C8 inhibition + 0.7999 79.99%
CYP inhibitory promiscuity - 0.6219 62.19%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.4602 46.02%
Eye corrosion - 0.9879 98.79%
Eye irritation - 0.8959 89.59%
Skin irritation - 0.7822 78.22%
Skin corrosion - 0.9173 91.73%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6838 68.38%
Micronuclear - 0.6100 61.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation - 0.7568 75.68%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.5567 55.67%
Acute Oral Toxicity (c) III 0.5716 57.16%
Estrogen receptor binding + 0.7931 79.31%
Androgen receptor binding + 0.7091 70.91%
Thyroid receptor binding + 0.6843 68.43%
Glucocorticoid receptor binding + 0.7872 78.72%
Aromatase binding + 0.6413 64.13%
PPAR gamma + 0.7241 72.41%
Honey bee toxicity - 0.6999 69.99%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.9419 94.19%

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
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 99.43% 89.34%
CHEMBL2581 P07339 Cathepsin D 98.59% 98.95%
CHEMBL2996 Q05655 Protein kinase C delta 98.07% 97.79%
CHEMBL1293249 Q13887 Kruppel-like factor 5 97.70% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.35% 91.11%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 96.00% 81.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.88% 99.23%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 92.21% 91.07%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 91.11% 87.67%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.95% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.24% 97.25%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 88.90% 96.77%
CHEMBL3524 P56524 Histone deacetylase 4 88.05% 92.97%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 87.87% 96.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.92% 89.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.45% 97.14%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 83.27% 96.39%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 82.99% 83.00%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 82.80% 97.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.58% 100.00%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 82.54% 98.75%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.50% 95.89%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.30% 85.14%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 81.90% 91.24%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 81.71% 93.65%
CHEMBL3975 P09467 Fructose-1,6-bisphosphatase 81.54% 92.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.27% 94.00%
CHEMBL1902 P62942 FK506-binding protein 1A 80.86% 97.05%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Euphorbia prolifera

Cross-Links

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PubChem 60168065
LOTUS LTS0048075
wikiData Q105342235