Isoevonine

Details

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Internal ID 59e5c6c3-6fd0-44bd-b4de-2d11a9450783
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones
IUPAC Name (19,20,22,25-tetraacetyloxy-26-hydroxy-3,15,26-trimethyl-6,16,23-trioxo-2,5,17-trioxa-11-azapentacyclo[16.7.1.01,21.03,24.07,12]hexacosa-7(12),8,10-trien-21-yl)methyl acetate
SMILES (Canonical) CC1CCC2=C(C=CC=N2)C(=O)OCC3(C4C(C5(O3)C(C(C(C(C5(C(C4=O)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C)OC1=O)(C)O)OC(=O)C)C
SMILES (Isomeric) CC1CCC2=C(C=CC=N2)C(=O)OCC3(C4C(C5(O3)C(C(C(C(C5(C(C4=O)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C)OC1=O)(C)O)OC(=O)C)C
InChI InChI=1S/C36H43NO17/c1-16-11-12-23-22(10-9-13-37-23)32(45)48-14-33(7)24-25(43)28(51-20(5)41)35(15-47-17(2)38)30(52-21(6)42)26(49-18(3)39)29(53-31(16)44)34(8,46)36(35,54-33)27(24)50-19(4)40/h9-10,13,16,24,26-30,46H,11-12,14-15H2,1-8H3
InChI Key QFMYKKJPSVFBKJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C36H43NO17
Molecular Weight 761.70 g/mol
Exact Mass 761.25309890 g/mol
Topological Polar Surface Area (TPSA) 244.00 Ų
XlogP 0.10
Atomic LogP (AlogP) 0.50
H-Bond Acceptor 18
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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QFMYKKJPSVFBKJ-UHFFFAOYSA-N

2D Structure

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2D Structure of Isoevonine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8926 89.26%
Caco-2 - 0.8336 83.36%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6200 62.00%
OATP2B1 inhibitior - 0.7141 71.41%
OATP1B1 inhibitior + 0.8394 83.94%
OATP1B3 inhibitior + 0.9110 91.10%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior + 0.9756 97.56%
P-glycoprotein inhibitior + 0.8504 85.04%
P-glycoprotein substrate + 0.6995 69.95%
CYP3A4 substrate + 0.7212 72.12%
CYP2C9 substrate + 0.5930 59.30%
CYP2D6 substrate - 0.8804 88.04%
CYP3A4 inhibition - 0.8451 84.51%
CYP2C9 inhibition - 0.7636 76.36%
CYP2C19 inhibition - 0.7663 76.63%
CYP2D6 inhibition - 0.9475 94.75%
CYP1A2 inhibition - 0.6664 66.64%
CYP2C8 inhibition + 0.7393 73.93%
CYP inhibitory promiscuity - 0.7114 71.14%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5304 53.04%
Eye corrosion - 0.9902 99.02%
Eye irritation - 0.9001 90.01%
Skin irritation - 0.7921 79.21%
Skin corrosion - 0.9322 93.22%
Ames mutagenesis - 0.6270 62.70%
Human Ether-a-go-go-Related Gene inhibition - 0.4942 49.42%
Micronuclear - 0.6600 66.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation - 0.8729 87.29%
Respiratory toxicity + 0.7778 77.78%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity + 0.6983 69.83%
Acute Oral Toxicity (c) III 0.5474 54.74%
Estrogen receptor binding + 0.7982 79.82%
Androgen receptor binding + 0.7381 73.81%
Thyroid receptor binding + 0.6228 62.28%
Glucocorticoid receptor binding + 0.7428 74.28%
Aromatase binding + 0.6675 66.75%
PPAR gamma + 0.7741 77.41%
Honey bee toxicity - 0.7237 72.37%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.6835 68.35%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.42% 96.09%
CHEMBL2581 P07339 Cathepsin D 97.04% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.83% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.12% 97.25%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.21% 85.14%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 93.74% 82.69%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.11% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.11% 89.00%
CHEMBL1951 P21397 Monoamine oxidase A 90.51% 91.49%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 90.48% 96.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.42% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.60% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.59% 99.23%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 87.81% 95.17%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 87.63% 93.10%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.50% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.02% 97.09%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 82.71% 81.11%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 82.24% 94.42%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.09% 96.00%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 81.21% 96.67%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.04% 95.89%
CHEMBL1937 Q92769 Histone deacetylase 2 80.87% 94.75%

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.
Euonymus europaeus
Euonymus nanus

Cross-Links

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PubChem 538503
LOTUS LTS0223806
wikiData Q105219662