[(1S,2R,3R,4R,5R,6R,7S,9R,12R)-4,12-diacetyloxy-5-benzoyloxy-3-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate

Details

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Internal ID 6a9d8526-afd9-4f8d-81d5-370d3e017a2d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Agarofurans
IUPAC Name [(1S,2R,3R,4R,5R,6R,7S,9R,12R)-4,12-diacetyloxy-5-benzoyloxy-3-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate
SMILES (Canonical) CC1C(C(C(C2(C13C(C(CC2OC(=O)C4=CC=CC=C4)C(O3)(C)C)OC(=O)C)C)OC(=O)C5=CC=CC=C5)OC(=O)C)O
SMILES (Isomeric) C[C@@H]1[C@H]([C@H]([C@@H]([C@@]2([C@]13[C@@H]([C@@H](C[C@@H]2OC(=O)C4=CC=CC=C4)C(O3)(C)C)OC(=O)C)C)OC(=O)C5=CC=CC=C5)OC(=O)C)O
InChI InChI=1S/C33H38O10/c1-18-25(36)26(39-19(2)34)28(42-30(38)22-15-11-8-12-16-22)32(6)24(41-29(37)21-13-9-7-10-14-21)17-23-27(40-20(3)35)33(18,32)43-31(23,4)5/h7-16,18,23-28,36H,17H2,1-6H3/t18-,23-,24+,25-,26-,27-,28+,32-,33-/m1/s1
InChI Key SOTGPCCKMHIJCT-IUYQRIQESA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C33H38O10
Molecular Weight 594.60 g/mol
Exact Mass 594.24649740 g/mol
Topological Polar Surface Area (TPSA) 135.00 Ų
XlogP 4.50
Atomic LogP (AlogP) 3.89
H-Bond Acceptor 10
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(1S,2R,3R,4R,5R,6R,7S,9R,12R)-4,12-diacetyloxy-5-benzoyloxy-3-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate

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 - 0.7307 73.07%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.6608 66.08%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8374 83.74%
OATP1B3 inhibitior + 0.8454 84.54%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.9223 92.23%
P-glycoprotein inhibitior + 0.9114 91.14%
P-glycoprotein substrate - 0.6494 64.94%
CYP3A4 substrate + 0.6424 64.24%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8409 84.09%
CYP3A4 inhibition - 0.8349 83.49%
CYP2C9 inhibition - 0.8828 88.28%
CYP2C19 inhibition - 0.9028 90.28%
CYP2D6 inhibition - 0.9412 94.12%
CYP1A2 inhibition - 0.8849 88.49%
CYP2C8 inhibition + 0.6412 64.12%
CYP inhibitory promiscuity - 0.9199 91.99%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.4688 46.88%
Eye corrosion - 0.9893 98.93%
Eye irritation - 0.8895 88.95%
Skin irritation - 0.7774 77.74%
Skin corrosion - 0.9290 92.90%
Ames mutagenesis - 0.6137 61.37%
Human Ether-a-go-go-Related Gene inhibition + 0.7331 73.31%
Micronuclear - 0.5241 52.41%
Hepatotoxicity - 0.6625 66.25%
skin sensitisation - 0.8049 80.49%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity + 0.5724 57.24%
Acute Oral Toxicity (c) III 0.4849 48.49%
Estrogen receptor binding + 0.7906 79.06%
Androgen receptor binding + 0.6308 63.08%
Thyroid receptor binding + 0.6279 62.79%
Glucocorticoid receptor binding + 0.6987 69.87%
Aromatase binding + 0.5959 59.59%
PPAR gamma + 0.7223 72.23%
Honey bee toxicity - 0.8193 81.93%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5755 57.55%
Fish aquatic toxicity + 0.9841 98.41%

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 96.24% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 94.07% 90.17%
CHEMBL2581 P07339 Cathepsin D 93.60% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.25% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.65% 99.23%
CHEMBL1951 P21397 Monoamine oxidase A 90.31% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.19% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.66% 95.56%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 89.24% 97.14%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 89.02% 94.62%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 88.64% 81.11%
CHEMBL340 P08684 Cytochrome P450 3A4 85.98% 91.19%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.87% 95.50%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 83.50% 83.00%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 83.05% 94.08%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.81% 82.69%
CHEMBL5028 O14672 ADAM10 82.06% 97.50%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.39% 89.00%
CHEMBL2535 P11166 Glucose transporter 80.68% 98.75%

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.
Maytenus boaria

Cross-Links

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PubChem 134151675
LOTUS LTS0197567
wikiData Q105257180