Turrapubin E

Details

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Internal ID 0be30b0d-a30e-4dcd-8a02-595fb981b242
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids > Limonoids
IUPAC Name methyl 2-[(1R,2S)-2-[(1aR,3S,3aR,4R,5R,6R,7aS)-5-acetyloxy-3-(furan-3-yl)-4-hydroxy-3a-methyl-7-methylidene-1a,2,3,4,5,6-hexahydroindeno[1,7a-b]oxiren-6-yl]-2,6,6-trimethyl-5-oxocyclohex-3-en-1-yl]acetate
SMILES (Canonical) CC(=O)OC1C(C(=C)C23C(O2)CC(C3(C1O)C)C4=COC=C4)C5(C=CC(=O)C(C5CC(=O)OC)(C)C)C
SMILES (Isomeric) CC(=O)O[C@@H]1[C@@H](C(=C)[C@]23[C@H](O2)C[C@H]([C@@]3([C@H]1O)C)C4=COC=C4)[C@]5(C=CC(=O)C([C@@H]5CC(=O)OC)(C)C)C
InChI InChI=1S/C29H36O8/c1-15-23(27(5)10-8-20(31)26(3,4)19(27)13-22(32)34-7)24(36-16(2)30)25(33)28(6)18(17-9-11-35-14-17)12-21-29(15,28)37-21/h8-11,14,18-19,21,23-25,33H,1,12-13H2,2-7H3/t18-,19-,21+,23+,24+,25-,27-,28+,29+/m0/s1
InChI Key SSWQNQTXPXQVMO-DFLDTDNRSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C29H36O8
Molecular Weight 512.60 g/mol
Exact Mass 512.24101810 g/mol
Topological Polar Surface Area (TPSA) 116.00 Ų
XlogP 2.50
Atomic LogP (AlogP) 3.74
H-Bond Acceptor 8
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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CHEMBL2386293

2D Structure

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2D Structure of Turrapubin E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9688 96.88%
Caco-2 - 0.7103 71.03%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.7170 71.70%
OATP2B1 inhibitior - 0.8572 85.72%
OATP1B1 inhibitior - 0.3603 36.03%
OATP1B3 inhibitior - 0.3367 33.67%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.9765 97.65%
P-glycoprotein inhibitior + 0.7637 76.37%
P-glycoprotein substrate + 0.6483 64.83%
CYP3A4 substrate + 0.7065 70.65%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8691 86.91%
CYP3A4 inhibition + 0.8779 87.79%
CYP2C9 inhibition - 0.6988 69.88%
CYP2C19 inhibition - 0.6546 65.46%
CYP2D6 inhibition - 0.8993 89.93%
CYP1A2 inhibition - 0.8501 85.01%
CYP2C8 inhibition + 0.6669 66.69%
CYP inhibitory promiscuity - 0.5351 53.51%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.4443 44.43%
Eye corrosion - 0.9859 98.59%
Eye irritation - 0.9161 91.61%
Skin irritation - 0.6999 69.99%
Skin corrosion - 0.9204 92.04%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4416 44.16%
Micronuclear - 0.5500 55.00%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.7410 74.10%
Respiratory toxicity + 0.8556 85.56%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.5553 55.53%
Acute Oral Toxicity (c) I 0.3697 36.97%
Estrogen receptor binding + 0.7157 71.57%
Androgen receptor binding + 0.7308 73.08%
Thyroid receptor binding + 0.6218 62.18%
Glucocorticoid receptor binding + 0.8115 81.15%
Aromatase binding + 0.5892 58.92%
PPAR gamma + 0.7133 71.33%
Honey bee toxicity - 0.7653 76.53%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9827 98.27%

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 98.88% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.24% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.84% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.81% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.76% 94.00%
CHEMBL340 P08684 Cytochrome P450 3A4 88.91% 91.19%
CHEMBL2581 P07339 Cathepsin D 88.22% 98.95%
CHEMBL3922 P50579 Methionine aminopeptidase 2 86.27% 97.28%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.69% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.19% 95.56%
CHEMBL4208 P20618 Proteasome component C5 84.85% 90.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.83% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.60% 95.89%
CHEMBL2996 Q05655 Protein kinase C delta 83.02% 97.79%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.73% 99.17%
CHEMBL5028 O14672 ADAM10 81.35% 97.50%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.06% 96.00%
CHEMBL221 P23219 Cyclooxygenase-1 80.60% 90.17%

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.
Turraea pubescens

Cross-Links

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PubChem 71725866
LOTUS LTS0227225
wikiData Q105259999