[(1S,2S,3R,6R,7S,8S,9R,13S)-13-acetyloxy-6-hydroxy-3,8-dimethyl-12-methylidene-4,11-dioxo-10-oxatricyclo[7.3.1.03,7]tridecan-2-yl] (Z)-2-methylbut-2-enoate

Details

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Internal ID 181ed6db-779f-4194-a626-caad1d6064ec
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Tricarboxylic acids and derivatives
IUPAC Name [(1S,2S,3R,6R,7S,8S,9R,13S)-13-acetyloxy-6-hydroxy-3,8-dimethyl-12-methylidene-4,11-dioxo-10-oxatricyclo[7.3.1.03,7]tridecan-2-yl] (Z)-2-methylbut-2-enoate
SMILES (Canonical) CC=C(C)C(=O)OC1C2C(C(C(C3C1(C(=O)CC3O)C)C)OC(=O)C2=C)OC(=O)C
SMILES (Isomeric) C/C=C(/C)\C(=O)O[C@H]1[C@H]2[C@@H]([C@@H]([C@H]([C@H]3[C@]1(C(=O)C[C@H]3O)C)C)OC(=O)C2=C)OC(=O)C
InChI InChI=1S/C22H28O8/c1-7-9(2)20(26)30-19-15-10(3)21(27)29-17(18(15)28-12(5)23)11(4)16-13(24)8-14(25)22(16,19)6/h7,11,13,15-19,24H,3,8H2,1-2,4-6H3/b9-7-/t11-,13+,15+,16+,17+,18-,19-,22+/m0/s1
InChI Key WDISZEOAIVKJTA-SIPLVVKMSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H28O8
Molecular Weight 420.50 g/mol
Exact Mass 420.17841785 g/mol
Topological Polar Surface Area (TPSA) 116.00 Ų
XlogP 1.80
Atomic LogP (AlogP) 1.50
H-Bond Acceptor 8
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(1S,2S,3R,6R,7S,8S,9R,13S)-13-acetyloxy-6-hydroxy-3,8-dimethyl-12-methylidene-4,11-dioxo-10-oxatricyclo[7.3.1.03,7]tridecan-2-yl] (Z)-2-methylbut-2-enoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9726 97.26%
Caco-2 - 0.5218 52.18%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.5063 50.63%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8288 82.88%
OATP1B3 inhibitior + 0.9332 93.32%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.6117 61.17%
P-glycoprotein inhibitior + 0.6303 63.03%
P-glycoprotein substrate - 0.6463 64.63%
CYP3A4 substrate + 0.6394 63.94%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.9018 90.18%
CYP3A4 inhibition - 0.5775 57.75%
CYP2C9 inhibition - 0.9554 95.54%
CYP2C19 inhibition - 0.8968 89.68%
CYP2D6 inhibition - 0.9567 95.67%
CYP1A2 inhibition - 0.8468 84.68%
CYP2C8 inhibition - 0.7443 74.43%
CYP inhibitory promiscuity - 0.9704 97.04%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6071 60.71%
Eye corrosion - 0.9786 97.86%
Eye irritation - 0.8469 84.69%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.8774 87.74%
Ames mutagenesis - 0.5978 59.78%
Human Ether-a-go-go-Related Gene inhibition - 0.5314 53.14%
Micronuclear - 0.5800 58.00%
Hepatotoxicity + 0.7168 71.68%
skin sensitisation - 0.6769 67.69%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity + 0.8216 82.16%
Acute Oral Toxicity (c) II 0.3711 37.11%
Estrogen receptor binding + 0.7267 72.67%
Androgen receptor binding + 0.6075 60.75%
Thyroid receptor binding - 0.5373 53.73%
Glucocorticoid receptor binding + 0.5834 58.34%
Aromatase binding - 0.5881 58.81%
PPAR gamma + 0.6688 66.88%
Honey bee toxicity - 0.6358 63.58%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.8954 89.54%

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 97.40% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 95.23% 90.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 94.42% 99.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.71% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.62% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.73% 95.56%
CHEMBL241 Q14432 Phosphodiesterase 3A 88.94% 92.94%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.62% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.73% 96.09%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 86.37% 95.50%
CHEMBL2581 P07339 Cathepsin D 86.26% 98.95%
CHEMBL325 Q13547 Histone deacetylase 1 85.04% 95.92%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 84.01% 91.07%
CHEMBL2996 Q05655 Protein kinase C delta 83.08% 97.79%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 82.84% 97.21%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.04% 89.00%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 81.94% 93.00%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 80.84% 96.00%
CHEMBL340 P08684 Cytochrome P450 3A4 80.50% 91.19%

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.
Tetraneuris ivesiana
Tetraneuris linearifolia

Cross-Links

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PubChem 14807539
LOTUS LTS0173651
wikiData Q105302389