Esulatin L

Details

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Internal ID c01755b4-6ede-48d0-b51d-f4b89f10baf7
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Jatrophane and cyclojatrophane diterpenoids
IUPAC Name [(1R,2R,3aR,5R,6E,9R,11R,13R,13aS)-1,2,3a,13-tetraacetyloxy-2,5,8,8-tetramethyl-12-methylidene-11-(2-methylpropoxy)-4-oxo-1,3,5,9,10,11,13,13a-octahydrocyclopenta[12]annulen-9-yl] pyridine-3-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C38H51NO12/c1-21(2)19-46-29-17-30(49-35(45)28-13-12-16-39-18-28)36(9,10)15-14-22(3)33(44)38(51-27(8)43)20-37(11,50-26(7)42)34(48-25(6)41)31(38)32(23(29)4)47-24(5)40/h12-16,18,21-22,29-32,34H,4,17,19-20H2,1-3,5-11H3/b15-14+/t22-,29-,30-,31+,32+,34-,37-,38-/m1/s1
InChI Key GEQXZNXXYBZFOZ-BGJWXCAQSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C38H51NO12
Molecular Weight 713.80 g/mol
Exact Mass 713.34112606 g/mol
Topological Polar Surface Area (TPSA) 171.00 Ų
XlogP 4.70
Atomic LogP (AlogP) 4.90
H-Bond Acceptor 13
H-Bond Donor 0
Rotatable Bonds 9

Synonyms

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CHEMBL1812477

2D Structure

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2D Structure of Esulatin L

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9852 98.52%
Caco-2 - 0.8351 83.51%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.7380 73.80%
OATP2B1 inhibitior - 0.5683 56.83%
OATP1B1 inhibitior + 0.8505 85.05%
OATP1B3 inhibitior + 0.8839 88.39%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9961 99.61%
P-glycoprotein inhibitior + 0.9175 91.75%
P-glycoprotein substrate + 0.6501 65.01%
CYP3A4 substrate + 0.7005 70.05%
CYP2C9 substrate - 0.8021 80.21%
CYP2D6 substrate - 0.8816 88.16%
CYP3A4 inhibition + 0.5966 59.66%
CYP2C9 inhibition - 0.7318 73.18%
CYP2C19 inhibition - 0.5953 59.53%
CYP2D6 inhibition - 0.9070 90.70%
CYP1A2 inhibition + 0.5063 50.63%
CYP2C8 inhibition + 0.7995 79.95%
CYP inhibitory promiscuity + 0.5058 50.58%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.5740 57.40%
Eye corrosion - 0.9855 98.55%
Eye irritation - 0.9053 90.53%
Skin irritation - 0.7255 72.55%
Skin corrosion - 0.9407 94.07%
Ames mutagenesis - 0.5737 57.37%
Human Ether-a-go-go-Related Gene inhibition + 0.6422 64.22%
Micronuclear - 0.6300 63.00%
Hepatotoxicity + 0.6677 66.77%
skin sensitisation - 0.7176 71.76%
Respiratory toxicity + 0.8000 80.00%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.5834 58.34%
Acute Oral Toxicity (c) III 0.5871 58.71%
Estrogen receptor binding + 0.7454 74.54%
Androgen receptor binding + 0.7320 73.20%
Thyroid receptor binding + 0.6254 62.54%
Glucocorticoid receptor binding + 0.7946 79.46%
Aromatase binding + 0.6258 62.58%
PPAR gamma + 0.7658 76.58%
Honey bee toxicity - 0.6606 66.06%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9822 98.22%

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
CHEMBL2581 P07339 Cathepsin D 97.79% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.55% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 97.12% 86.33%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 96.34% 89.34%
CHEMBL2996 Q05655 Protein kinase C delta 95.63% 97.79%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.73% 97.25%
CHEMBL221 P23219 Cyclooxygenase-1 93.60% 90.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.46% 94.45%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 89.66% 98.75%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.95% 85.14%
CHEMBL2535 P11166 Glucose transporter 87.92% 98.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.13% 99.23%
CHEMBL1951 P21397 Monoamine oxidase A 86.31% 91.49%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.64% 95.89%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 85.62% 91.24%
CHEMBL4208 P20618 Proteasome component C5 85.45% 90.00%
CHEMBL3267 P48736 PI3-kinase p110-gamma subunit 84.63% 95.71%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.99% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.69% 97.09%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 83.16% 91.07%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 82.51% 93.10%
CHEMBL5028 O14672 ADAM10 81.52% 97.50%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.99% 89.00%
CHEMBL202 P00374 Dihydrofolate reductase 80.98% 89.92%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.97% 96.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 80.75% 94.80%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 80.51% 82.69%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.20% 94.00%

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 esula

Cross-Links

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PubChem 56669602
LOTUS LTS0275172
wikiData Q105007292