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

Details

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Internal ID 26cd4b62-0034-4e75-8c08-7b16946982af
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Agarofurans
IUPAC Name [(1R,2S,4R,5R,6R,7R,9S)-4-acetyloxy-5-benzoyloxy-2-hydroxy-2,6,10,10-tetramethyl-12-oxo-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate
SMILES (Canonical) CC(=O)OC1CC(C23C(=O)C(CC(C2(C1OC(=O)C4=CC=CC=C4)C)OC(=O)C5=CC=CC=C5)C(O3)(C)C)(C)O
SMILES (Isomeric) CC(=O)O[C@@H]1C[C@]([C@@]23C(=O)[C@@H](C[C@H]([C@@]2([C@H]1OC(=O)C4=CC=CC=C4)C)OC(=O)C5=CC=CC=C5)C(O3)(C)C)(C)O
InChI InChI=1S/C31H34O9/c1-18(32)37-22-17-29(4,36)31-24(33)21(28(2,3)40-31)16-23(38-26(34)19-12-8-6-9-13-19)30(31,5)25(22)39-27(35)20-14-10-7-11-15-20/h6-15,21-23,25,36H,16-17H2,1-5H3/t21-,22-,23-,25+,29+,30-,31+/m1/s1
InChI Key VDNJAHVVPAQKQE-JWOBBUFBSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C31H34O9
Molecular Weight 550.60 g/mol
Exact Mass 550.22028266 g/mol
Topological Polar Surface Area (TPSA) 125.00 Ų
XlogP 3.80
Atomic LogP (AlogP) 3.67
H-Bond Acceptor 9
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(1R,2S,4R,5R,6R,7R,9S)-4-acetyloxy-5-benzoyloxy-2-hydroxy-2,6,10,10-tetramethyl-12-oxo-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 + 0.9866 98.66%
Caco-2 - 0.6937 69.37%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.5348 53.48%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8830 88.30%
OATP1B3 inhibitior + 0.8334 83.34%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9464 94.64%
P-glycoprotein inhibitior + 0.8857 88.57%
P-glycoprotein substrate - 0.6560 65.60%
CYP3A4 substrate + 0.6683 66.83%
CYP2C9 substrate - 0.8042 80.42%
CYP2D6 substrate - 0.8562 85.62%
CYP3A4 inhibition - 0.6480 64.80%
CYP2C9 inhibition - 0.8353 83.53%
CYP2C19 inhibition - 0.8767 87.67%
CYP2D6 inhibition - 0.9464 94.64%
CYP1A2 inhibition - 0.8079 80.79%
CYP2C8 inhibition + 0.5810 58.10%
CYP inhibitory promiscuity - 0.9509 95.09%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.4768 47.68%
Eye corrosion - 0.9919 99.19%
Eye irritation - 0.8923 89.23%
Skin irritation - 0.7176 71.76%
Skin corrosion - 0.9082 90.82%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8086 80.86%
Micronuclear - 0.6500 65.00%
Hepatotoxicity - 0.5803 58.03%
skin sensitisation - 0.7905 79.05%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.5928 59.28%
Acute Oral Toxicity (c) III 0.4650 46.50%
Estrogen receptor binding + 0.7644 76.44%
Androgen receptor binding + 0.7224 72.24%
Thyroid receptor binding + 0.6680 66.80%
Glucocorticoid receptor binding + 0.7286 72.86%
Aromatase binding + 0.6143 61.43%
PPAR gamma + 0.6479 64.79%
Honey bee toxicity - 0.7671 76.71%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9884 98.84%

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 96.27% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.62% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 94.14% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.89% 95.56%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 90.03% 94.62%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 89.35% 83.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.93% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 88.43% 90.17%
CHEMBL340 P08684 Cytochrome P450 3A4 88.17% 91.19%
CHEMBL1951 P21397 Monoamine oxidase A 87.48% 91.49%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 87.44% 97.14%
CHEMBL4208 P20618 Proteasome component C5 86.32% 90.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.44% 95.50%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.17% 97.09%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 85.08% 94.08%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 85.01% 81.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.45% 85.14%
CHEMBL2581 P07339 Cathepsin D 84.20% 98.95%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.14% 95.89%
CHEMBL5028 O14672 ADAM10 80.03% 97.50%

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.
Mortonia greggii

Cross-Links

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PubChem 162909035
LOTUS LTS0242972
wikiData Q105284270