Methyl 2-[14-acetyloxy-6-(furan-3-yl)-17-hydroxy-1,5,15-trimethyl-8,12-dioxo-7-oxapentacyclo[13.2.1.02,11.05,10.013,17]octadec-10-en-18-yl]acetate

Details

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Internal ID 3f5d6e9d-9b1f-4f82-95ad-d9cd7b98bf5a
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids > Limonoids
IUPAC Name methyl 2-[14-acetyloxy-6-(furan-3-yl)-17-hydroxy-1,5,15-trimethyl-8,12-dioxo-7-oxapentacyclo[13.2.1.02,11.05,10.013,17]octadec-10-en-18-yl]acetate
SMILES (Canonical) CC(=O)OC1C2C(=O)C3=C4CC(=O)OC(C4(CCC3C5(C2(CC1(C5CC(=O)OC)C)O)C)C)C6=COC=C6
SMILES (Isomeric) CC(=O)OC1C2C(=O)C3=C4CC(=O)OC(C4(CCC3C5(C2(CC1(C5CC(=O)OC)C)O)C)C)C6=COC=C6
InChI InChI=1S/C29H34O9/c1-14(30)37-25-22-23(33)21-16(28(4)18(11-19(31)35-5)27(25,3)13-29(22,28)34)6-8-26(2)17(21)10-20(32)38-24(26)15-7-9-36-12-15/h7,9,12,16,18,22,24-25,34H,6,8,10-11,13H2,1-5H3
InChI Key LSBZEHLCUALPOF-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C29H34O9
Molecular Weight 526.60 g/mol
Exact Mass 526.22028266 g/mol
Topological Polar Surface Area (TPSA) 129.00 Ų
XlogP 1.80
Atomic LogP (AlogP) 3.45
H-Bond Acceptor 9
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Methyl 2-[14-acetyloxy-6-(furan-3-yl)-17-hydroxy-1,5,15-trimethyl-8,12-dioxo-7-oxapentacyclo[13.2.1.02,11.05,10.013,17]octadec-10-en-18-yl]acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9877 98.77%
Caco-2 - 0.7057 70.57%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.8164 81.64%
OATP2B1 inhibitior - 0.7185 71.85%
OATP1B1 inhibitior - 0.5212 52.12%
OATP1B3 inhibitior + 0.9258 92.58%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.9743 97.43%
P-glycoprotein inhibitior + 0.7762 77.62%
P-glycoprotein substrate + 0.6012 60.12%
CYP3A4 substrate + 0.6963 69.63%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8959 89.59%
CYP3A4 inhibition + 0.7095 70.95%
CYP2C9 inhibition - 0.8546 85.46%
CYP2C19 inhibition - 0.9054 90.54%
CYP2D6 inhibition - 0.9286 92.86%
CYP1A2 inhibition - 0.7826 78.26%
CYP2C8 inhibition + 0.7238 72.38%
CYP inhibitory promiscuity - 0.7817 78.17%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.4513 45.13%
Eye corrosion - 0.9921 99.21%
Eye irritation - 0.8771 87.71%
Skin irritation - 0.5386 53.86%
Skin corrosion - 0.9274 92.74%
Ames mutagenesis - 0.6170 61.70%
Human Ether-a-go-go-Related Gene inhibition + 0.6850 68.50%
Micronuclear - 0.6200 62.00%
Hepatotoxicity + 0.5603 56.03%
skin sensitisation - 0.8827 88.27%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.9889 98.89%
Mitochondrial toxicity + 0.9375 93.75%
Nephrotoxicity + 0.4783 47.83%
Acute Oral Toxicity (c) I 0.6788 67.88%
Estrogen receptor binding + 0.8703 87.03%
Androgen receptor binding + 0.7506 75.06%
Thyroid receptor binding + 0.6267 62.67%
Glucocorticoid receptor binding + 0.8173 81.73%
Aromatase binding + 0.7636 76.36%
PPAR gamma + 0.8065 80.65%
Honey bee toxicity - 0.7958 79.58%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.9915 99.15%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 99.31% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.51% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.91% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.31% 85.14%
CHEMBL5608 Q16288 NT-3 growth factor receptor 91.22% 95.89%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 90.26% 94.33%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 90.23% 91.24%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.31% 86.33%
CHEMBL221 P23219 Cyclooxygenase-1 87.92% 90.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.67% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.47% 100.00%
CHEMBL340 P08684 Cytochrome P450 3A4 83.66% 91.19%
CHEMBL4208 P20618 Proteasome component C5 83.51% 90.00%
CHEMBL5255 O00206 Toll-like receptor 4 83.42% 92.50%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 82.96% 92.88%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 82.83% 95.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.82% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.48% 94.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.08% 92.62%
CHEMBL3922 P50579 Methionine aminopeptidase 2 81.62% 97.28%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.11% 97.14%

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.
Xylocarpus moluccensis

Cross-Links

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PubChem 75165809
LOTUS LTS0124931
wikiData Q105156463