[(1S,7E,9S,12S,13S,14S)-14-acetyloxy-9-hydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.03,7]heptadeca-3,7,16-trien-12-yl] 3-methylbutanoate

Details

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Internal ID f1b8ffad-b19b-43f9-8175-e6a6af433b5d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Diterpene lactones
IUPAC Name [(1S,7E,9S,12S,13S,14S)-14-acetyloxy-9-hydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.03,7]heptadeca-3,7,16-trien-12-yl] 3-methylbutanoate
SMILES (Canonical) CC1=CCC(C2(C1CC3=C(C(=O)OC3=CC(CCC2OC(=O)CC(C)C)(C)O)C)C)OC(=O)C
SMILES (Isomeric) CC1=CC[C@@H]([C@]2([C@H]1CC\3=C(C(=O)O/C3=C/[C@@](CC[C@@H]2OC(=O)CC(C)C)(C)O)C)C)OC(=O)C
InChI InChI=1S/C27H38O7/c1-15(2)12-24(29)34-23-10-11-26(6,31)14-21-19(17(4)25(30)33-21)13-20-16(3)8-9-22(27(20,23)7)32-18(5)28/h8,14-15,20,22-23,31H,9-13H2,1-7H3/b21-14+/t20-,22-,23-,26-,27+/m0/s1
InChI Key BLGNMWVTJWYRRQ-PSWUVOTOSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C27H38O7
Molecular Weight 474.60 g/mol
Exact Mass 474.26175355 g/mol
Topological Polar Surface Area (TPSA) 99.10 Ų
XlogP 3.50
Atomic LogP (AlogP) 4.54
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(1S,7E,9S,12S,13S,14S)-14-acetyloxy-9-hydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.03,7]heptadeca-3,7,16-trien-12-yl] 3-methylbutanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9948 99.48%
Caco-2 + 0.5096 50.96%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7880 78.80%
OATP2B1 inhibitior - 0.8567 85.67%
OATP1B1 inhibitior + 0.8507 85.07%
OATP1B3 inhibitior - 0.2528 25.28%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior + 0.9730 97.30%
P-glycoprotein inhibitior + 0.8001 80.01%
P-glycoprotein substrate - 0.5943 59.43%
CYP3A4 substrate + 0.6924 69.24%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9107 91.07%
CYP3A4 inhibition - 0.5813 58.13%
CYP2C9 inhibition - 0.6831 68.31%
CYP2C19 inhibition - 0.8866 88.66%
CYP2D6 inhibition - 0.9547 95.47%
CYP1A2 inhibition - 0.7188 71.88%
CYP2C8 inhibition + 0.4625 46.25%
CYP inhibitory promiscuity - 0.9041 90.41%
UGT catelyzed - 0.8000 80.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5891 58.91%
Eye corrosion - 0.9870 98.70%
Eye irritation - 0.8840 88.40%
Skin irritation + 0.5504 55.04%
Skin corrosion - 0.8807 88.07%
Ames mutagenesis - 0.5770 57.70%
Human Ether-a-go-go-Related Gene inhibition - 0.3818 38.18%
Micronuclear - 0.7800 78.00%
Hepatotoxicity + 0.6858 68.58%
skin sensitisation - 0.7374 73.74%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity - 0.6772 67.72%
Acute Oral Toxicity (c) III 0.3504 35.04%
Estrogen receptor binding + 0.8963 89.63%
Androgen receptor binding + 0.5950 59.50%
Thyroid receptor binding + 0.6701 67.01%
Glucocorticoid receptor binding + 0.8590 85.90%
Aromatase binding + 0.7511 75.11%
PPAR gamma + 0.8169 81.69%
Honey bee toxicity - 0.8014 80.14%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5950 59.50%
Fish aquatic toxicity + 0.9799 97.99%

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 97.78% 96.09%
CHEMBL2581 P07339 Cathepsin D 96.08% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.58% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.01% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.97% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.25% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.64% 86.33%
CHEMBL5103 Q969S8 Histone deacetylase 10 88.57% 90.08%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.12% 92.62%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.83% 94.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.25% 97.09%
CHEMBL3359 P21462 Formyl peptide receptor 1 85.68% 93.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.70% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.62% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.56% 95.56%
CHEMBL5028 O14672 ADAM10 83.26% 97.50%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.65% 93.04%
CHEMBL1937 Q92769 Histone deacetylase 2 82.43% 94.75%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 81.50% 95.71%
CHEMBL3401 O75469 Pregnane X receptor 80.06% 94.73%

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.
Beta vulgaris

Cross-Links

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PubChem 162938012
LOTUS LTS0111445
wikiData Q104944903