(12-Hydroxy-5,10,15-trimethyl-14-oxo-4,9,13-trioxatetracyclo[10.3.0.03,5.08,10]pentadec-1(15)-en-2-yl) acetate

Details

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Internal ID afa27a85-a294-4435-a0b0-287ece573dac
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones
IUPAC Name (12-hydroxy-5,10,15-trimethyl-14-oxo-4,9,13-trioxatetracyclo[10.3.0.03,5.08,10]pentadec-1(15)-en-2-yl) acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H22O7/c1-8-11-12(21-9(2)18)13-15(3,23-13)6-5-10-16(4,22-10)7-17(11,20)24-14(8)19/h10,12-13,20H,5-7H2,1-4H3
InChI Key GXJGHGBQYRVFBB-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H22O7
Molecular Weight 338.40 g/mol
Exact Mass 338.13655304 g/mol
Topological Polar Surface Area (TPSA) 97.90 Ų
XlogP -0.10
Atomic LogP (AlogP) 0.98
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (12-Hydroxy-5,10,15-trimethyl-14-oxo-4,9,13-trioxatetracyclo[10.3.0.03,5.08,10]pentadec-1(15)-en-2-yl) acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9849 98.49%
Caco-2 + 0.6420 64.20%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.7119 71.19%
OATP2B1 inhibitior - 0.8597 85.97%
OATP1B1 inhibitior + 0.9316 93.16%
OATP1B3 inhibitior + 0.9240 92.40%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.6271 62.71%
BSEP inhibitior - 0.6064 60.64%
P-glycoprotein inhibitior - 0.6130 61.30%
P-glycoprotein substrate - 0.7679 76.79%
CYP3A4 substrate + 0.6672 66.72%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8851 88.51%
CYP3A4 inhibition - 0.6451 64.51%
CYP2C9 inhibition - 0.7901 79.01%
CYP2C19 inhibition - 0.8935 89.35%
CYP2D6 inhibition - 0.9434 94.34%
CYP1A2 inhibition + 0.5109 51.09%
CYP2C8 inhibition - 0.7491 74.91%
CYP inhibitory promiscuity - 0.9735 97.35%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.4228 42.28%
Eye corrosion - 0.9830 98.30%
Eye irritation - 0.8410 84.10%
Skin irritation + 0.5637 56.37%
Skin corrosion - 0.8927 89.27%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5959 59.59%
Micronuclear - 0.5800 58.00%
Hepatotoxicity + 0.6659 66.59%
skin sensitisation - 0.8208 82.08%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.8750 87.50%
Nephrotoxicity + 0.7647 76.47%
Acute Oral Toxicity (c) III 0.4203 42.03%
Estrogen receptor binding + 0.7301 73.01%
Androgen receptor binding + 0.6219 62.19%
Thyroid receptor binding + 0.6786 67.86%
Glucocorticoid receptor binding + 0.7506 75.06%
Aromatase binding - 0.5737 57.37%
PPAR gamma + 0.6739 67.39%
Honey bee toxicity - 0.7728 77.28%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5350 53.50%
Fish aquatic toxicity + 0.9629 96.29%

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 94.96% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.38% 91.11%
CHEMBL2581 P07339 Cathepsin D 91.47% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.80% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.39% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.71% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.73% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.72% 99.23%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 86.59% 97.14%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 85.99% 82.69%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.92% 86.33%
CHEMBL340 P08684 Cytochrome P450 3A4 83.43% 91.19%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.75% 95.89%
CHEMBL5028 O14672 ADAM10 81.66% 97.50%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.81% 93.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.66% 97.09%

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.
Salvia castanea

Cross-Links

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PubChem 162928991
LOTUS LTS0040734
wikiData Q105023091