(12-Acetyloxy-5,7-dibenzoyloxy-4-hexanoyloxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-8-yl) pyridine-3-carboxylate

Details

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Internal ID e48e3509-4ea9-4370-bffe-dda93f286dec
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Pentacarboxylic acids and derivatives
IUPAC Name (12-acetyloxy-5,7-dibenzoyloxy-4-hexanoyloxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-8-yl) pyridine-3-carboxylate
SMILES (Canonical) CCCCCC(=O)OC1CC(C23C(C(C(C(C2(C1OC(=O)C4=CC=CC=C4)C)OC(=O)C5=CC=CC=C5)OC(=O)C6=CN=CC=C6)C(O3)(C)C)OC(=O)C)C
SMILES (Isomeric) CCCCCC(=O)OC1CC(C23C(C(C(C(C2(C1OC(=O)C4=CC=CC=C4)C)OC(=O)C5=CC=CC=C5)OC(=O)C6=CN=CC=C6)C(O3)(C)C)OC(=O)C)C
InChI InChI=1S/C43H49NO11/c1-7-8-11-22-32(46)51-31-24-26(2)43-36(50-27(3)45)33(41(4,5)55-43)34(52-40(49)30-21-16-23-44-25-30)37(54-39(48)29-19-14-10-15-20-29)42(43,6)35(31)53-38(47)28-17-12-9-13-18-28/h9-10,12-21,23,25-26,31,33-37H,7-8,11,22,24H2,1-6H3
InChI Key OSZGZAKPYNKUDL-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C43H49NO11
Molecular Weight 755.80 g/mol
Exact Mass 755.33056138 g/mol
Topological Polar Surface Area (TPSA) 154.00 Ų
XlogP 7.60
Atomic LogP (AlogP) 6.71
H-Bond Acceptor 12
H-Bond Donor 0
Rotatable Bonds 12

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (12-Acetyloxy-5,7-dibenzoyloxy-4-hexanoyloxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-8-yl) pyridine-3-carboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9740 97.40%
Caco-2 - 0.8175 81.75%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.6976 69.76%
OATP2B1 inhibitior - 0.8527 85.27%
OATP1B1 inhibitior + 0.8268 82.68%
OATP1B3 inhibitior + 0.9052 90.52%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.9936 99.36%
P-glycoprotein inhibitior + 0.8952 89.52%
P-glycoprotein substrate + 0.6240 62.40%
CYP3A4 substrate + 0.6587 65.87%
CYP2C9 substrate - 0.8019 80.19%
CYP2D6 substrate - 0.8656 86.56%
CYP3A4 inhibition - 0.5070 50.70%
CYP2C9 inhibition - 0.8367 83.67%
CYP2C19 inhibition - 0.6851 68.51%
CYP2D6 inhibition - 0.9208 92.08%
CYP1A2 inhibition - 0.6949 69.49%
CYP2C8 inhibition + 0.8442 84.42%
CYP inhibitory promiscuity - 0.6901 69.01%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6081 60.81%
Eye corrosion - 0.9896 98.96%
Eye irritation - 0.9163 91.63%
Skin irritation - 0.7826 78.26%
Skin corrosion - 0.9154 91.54%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8701 87.01%
Micronuclear - 0.6800 68.00%
Hepatotoxicity - 0.5269 52.69%
skin sensitisation - 0.8669 86.69%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity + 0.5430 54.30%
Acute Oral Toxicity (c) III 0.5552 55.52%
Estrogen receptor binding + 0.7820 78.20%
Androgen receptor binding + 0.6472 64.72%
Thyroid receptor binding + 0.6565 65.65%
Glucocorticoid receptor binding + 0.7999 79.99%
Aromatase binding + 0.6343 63.43%
PPAR gamma + 0.7419 74.19%
Honey bee toxicity - 0.8323 83.23%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.7000 70.00%
Fish aquatic toxicity + 0.9865 98.65%

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
CHEMBL2996 Q05655 Protein kinase C delta 99.50% 97.79%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.22% 96.09%
CHEMBL2581 P07339 Cathepsin D 98.15% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 97.31% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.95% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 94.61% 90.17%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 94.52% 95.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.35% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 93.72% 99.23%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 89.19% 83.00%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 88.36% 94.62%
CHEMBL1951 P21397 Monoamine oxidase A 88.05% 91.49%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 87.91% 94.08%
CHEMBL1944495 P28065 Proteasome subunit beta type-9 86.75% 97.50%
CHEMBL5028 O14672 ADAM10 84.41% 97.50%
CHEMBL4227 P25090 Lipoxin A4 receptor 83.88% 100.00%
CHEMBL3891 P07384 Calpain 1 83.26% 93.04%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.98% 85.14%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.81% 95.89%
CHEMBL5255 O00206 Toll-like receptor 4 80.05% 92.50%

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.
Tripterygium wilfordii

Cross-Links

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PubChem 14828970
LOTUS LTS0248367
wikiData Q105199406