[(1S,2R,4S,5R,6S,7S,8R,9R,12R)-12-acetyloxy-4,5,7-tribenzoyloxy-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 8e927793-fd5a-4d1e-9d99-f8784a9efcbb
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Pentacarboxylic acids and derivatives
IUPAC Name [(1S,2R,4S,5R,6S,7S,8R,9R,12R)-12-acetyloxy-4,5,7-tribenzoyloxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-8-yl] pyridine-3-carboxylate
SMILES (Canonical) CC1CC(C(C2(C13C(C(C(C2OC(=O)C4=CC=CC=C4)OC(=O)C5=CN=CC=C5)C(O3)(C)C)OC(=O)C)C)OC(=O)C6=CC=CC=C6)OC(=O)C7=CC=CC=C7
SMILES (Isomeric) C[C@@H]1C[C@@H]([C@@H]([C@@]2([C@]13[C@@H]([C@@H]([C@H]([C@H]2OC(=O)C4=CC=CC=C4)OC(=O)C5=CN=CC=C5)C(O3)(C)C)OC(=O)C)C)OC(=O)C6=CC=CC=C6)OC(=O)C7=CC=CC=C7
InChI InChI=1S/C44H43NO11/c1-26-24-32(52-38(47)28-16-9-6-10-17-28)35(54-39(48)29-18-11-7-12-19-29)43(5)37(55-40(49)30-20-13-8-14-21-30)34(53-41(50)31-22-15-23-45-25-31)33-36(51-27(2)46)44(26,43)56-42(33,3)4/h6-23,25-26,32-37H,24H2,1-5H3/t26-,32+,33-,34-,35+,36-,37-,43+,44-/m1/s1
InChI Key FMSHZBLGSXKBSB-QHAVYKARSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C44H43NO11
Molecular Weight 761.80 g/mol
Exact Mass 761.28361119 g/mol
Topological Polar Surface Area (TPSA) 154.00 Ų
XlogP 7.30
Atomic LogP (AlogP) 6.44
H-Bond Acceptor 12
H-Bond Donor 0
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(1S,2R,4S,5R,6S,7S,8R,9R,12R)-12-acetyloxy-4,5,7-tribenzoyloxy-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 + 0.9558 95.58%
Caco-2 - 0.7863 78.63%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.5995 59.95%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8757 87.57%
OATP1B3 inhibitior + 0.9141 91.41%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9955 99.55%
P-glycoprotein inhibitior + 0.9361 93.61%
P-glycoprotein substrate - 0.6293 62.93%
CYP3A4 substrate + 0.6345 63.45%
CYP2C9 substrate - 0.8019 80.19%
CYP2D6 substrate - 0.8656 86.56%
CYP3A4 inhibition + 0.5461 54.61%
CYP2C9 inhibition - 0.8608 86.08%
CYP2C19 inhibition - 0.6439 64.39%
CYP2D6 inhibition - 0.9177 91.77%
CYP1A2 inhibition - 0.6805 68.05%
CYP2C8 inhibition + 0.7949 79.49%
CYP inhibitory promiscuity - 0.7035 70.35%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.4119 41.19%
Eye corrosion - 0.9889 98.89%
Eye irritation - 0.9017 90.17%
Skin irritation - 0.8181 81.81%
Skin corrosion - 0.9236 92.36%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8702 87.02%
Micronuclear - 0.5700 57.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation - 0.8074 80.74%
Respiratory toxicity + 0.8111 81.11%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity + 0.5793 57.93%
Acute Oral Toxicity (c) III 0.5529 55.29%
Estrogen receptor binding + 0.8054 80.54%
Androgen receptor binding + 0.6433 64.33%
Thyroid receptor binding + 0.7147 71.47%
Glucocorticoid receptor binding + 0.7814 78.14%
Aromatase binding + 0.6083 60.83%
PPAR gamma + 0.7281 72.81%
Honey bee toxicity - 0.7954 79.54%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5045 50.45%
Fish aquatic toxicity + 0.8898 88.98%

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 97.47% 97.79%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.72% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.53% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.15% 85.14%
CHEMBL2581 P07339 Cathepsin D 92.77% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.72% 99.23%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 92.39% 94.62%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.35% 91.11%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 90.63% 81.11%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 90.29% 83.00%
CHEMBL1951 P21397 Monoamine oxidase A 89.45% 91.49%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 89.38% 94.08%
CHEMBL221 P23219 Cyclooxygenase-1 86.98% 90.17%
CHEMBL5028 O14672 ADAM10 85.51% 97.50%
CHEMBL4208 P20618 Proteasome component C5 82.57% 90.00%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 81.83% 93.10%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.80% 91.07%

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 14828962
LOTUS LTS0200470
wikiData Q104998027