methyl (2R)-2-hydroxy-2-[(1R,2R,5R,6R,13S,16S)-6-[(2S)-2-hydroxy-5-oxo-2H-furan-4-yl]-1,5,15,15-tetramethyl-8,14,17-trioxo-7-oxatetracyclo[11.3.1.02,11.05,10]heptadec-10-en-16-yl]acetate

Details

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Internal ID 977c13e3-fc1c-4636-8718-ca079ac99ff2
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids > Limonoids
IUPAC Name methyl (2R)-2-hydroxy-2-[(1R,2R,5R,6R,13S,16S)-6-[(2S)-2-hydroxy-5-oxo-2H-furan-4-yl]-1,5,15,15-tetramethyl-8,14,17-trioxo-7-oxatetracyclo[11.3.1.02,11.05,10]heptadec-10-en-16-yl]acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H32O10/c1-25(2)19(18(30)24(34)35-5)27(4)14-6-7-26(3)15(11(14)8-12(20(25)31)21(27)32)10-17(29)36-22(26)13-9-16(28)37-23(13)33/h9,12,14,16,18-19,22,28,30H,6-8,10H2,1-5H3/t12-,14+,16-,18+,19-,22-,26+,27+/m0/s1
InChI Key ULLMXIDQKKNRAV-RLNJLFLDSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C27H32O10
Molecular Weight 516.50 g/mol
Exact Mass 516.19954721 g/mol
Topological Polar Surface Area (TPSA) 154.00 Ų
XlogP 0.70
Atomic LogP (AlogP) 1.17
H-Bond Acceptor 10
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of methyl (2R)-2-hydroxy-2-[(1R,2R,5R,6R,13S,16S)-6-[(2S)-2-hydroxy-5-oxo-2H-furan-4-yl]-1,5,15,15-tetramethyl-8,14,17-trioxo-7-oxatetracyclo[11.3.1.02,11.05,10]heptadec-10-en-16-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 + 0.9832 98.32%
Caco-2 - 0.7506 75.06%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.8396 83.96%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7917 79.17%
OATP1B3 inhibitior + 0.9232 92.32%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.5772 57.72%
P-glycoprotein inhibitior + 0.6257 62.57%
P-glycoprotein substrate + 0.5000 50.00%
CYP3A4 substrate + 0.6996 69.96%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.8855 88.55%
CYP3A4 inhibition - 0.5689 56.89%
CYP2C9 inhibition - 0.8577 85.77%
CYP2C19 inhibition - 0.9256 92.56%
CYP2D6 inhibition - 0.9443 94.43%
CYP1A2 inhibition - 0.8538 85.38%
CYP2C8 inhibition + 0.5555 55.55%
CYP inhibitory promiscuity - 0.8931 89.31%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Danger 0.4600 46.00%
Eye corrosion - 0.9895 98.95%
Eye irritation - 0.9256 92.56%
Skin irritation - 0.5759 57.59%
Skin corrosion - 0.9105 91.05%
Ames mutagenesis - 0.7737 77.37%
Human Ether-a-go-go-Related Gene inhibition - 0.5665 56.65%
Micronuclear - 0.6600 66.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation - 0.8455 84.55%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity - 0.6953 69.53%
Acute Oral Toxicity (c) I 0.6839 68.39%
Estrogen receptor binding + 0.7428 74.28%
Androgen receptor binding + 0.7094 70.94%
Thyroid receptor binding - 0.5186 51.86%
Glucocorticoid receptor binding + 0.7919 79.19%
Aromatase binding + 0.6738 67.38%
PPAR gamma + 0.6344 63.44%
Honey bee toxicity - 0.6247 62.47%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9849 98.49%

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 99.22% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.17% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 97.77% 90.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.08% 85.14%
CHEMBL4040 P28482 MAP kinase ERK2 92.10% 83.82%
CHEMBL2581 P07339 Cathepsin D 91.05% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.18% 97.25%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.03% 86.33%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 89.43% 82.69%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.22% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.61% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.55% 97.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.00% 99.23%
CHEMBL204 P00734 Thrombin 87.15% 96.01%
CHEMBL5028 O14672 ADAM10 86.63% 97.50%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.04% 92.62%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 84.00% 91.07%
CHEMBL4227 P25090 Lipoxin A4 receptor 83.57% 100.00%
CHEMBL340 P08684 Cytochrome P450 3A4 81.37% 91.19%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.19% 97.14%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 163026056
LOTUS LTS0083076
wikiData Q105275212