9-Acetoxy-8,10-Dehydrothymol 3-O-Tiglate

Details

Top
Internal ID b356add9-19fe-4dfd-b28c-e4202af50b53
Taxonomy Benzenoids > Phenol esters
IUPAC Name [2-(3-acetyloxyprop-1-en-2-yl)-5-methylphenyl] (E)-2-methylbut-2-enoate
SMILES (Canonical) CC=C(C)C(=O)OC1=C(C=CC(=C1)C)C(=C)COC(=O)C
SMILES (Isomeric) C/C=C(\C)/C(=O)OC1=C(C=CC(=C1)C)C(=C)COC(=O)C
InChI InChI=1S/C17H20O4/c1-6-12(3)17(19)21-16-9-11(2)7-8-15(16)13(4)10-20-14(5)18/h6-9H,4,10H2,1-3,5H3/b12-6+
InChI Key YQTJNXJVGGXRFW-WUXMJOGZSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C17H20O4
Molecular Weight 288.34 g/mol
Exact Mass 288.13615911 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 4.00
Atomic LogP (AlogP) 3.44
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

Top
CHEBI:67427
CHEMBL1795991
Q27135891
[2-(3-acetyloxyprop-1-en-2-yl)-5-methylphenyl] (E)-2-methylbut-2-enoate
(E)-2-Methyl-2-butenoic acid 2-[1-(acetoxymethyl)ethenyl]-5-methylphenyl ester

2D Structure

Top
2D Structure of 9-Acetoxy-8,10-Dehydrothymol 3-O-Tiglate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9962 99.62%
Caco-2 + 0.8039 80.39%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.8828 88.28%
OATP2B1 inhibitior - 0.8601 86.01%
OATP1B1 inhibitior + 0.9112 91.12%
OATP1B3 inhibitior + 0.9468 94.68%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.8498 84.98%
P-glycoprotein inhibitior - 0.7124 71.24%
P-glycoprotein substrate - 0.8486 84.86%
CYP3A4 substrate - 0.5393 53.93%
CYP2C9 substrate + 0.6016 60.16%
CYP2D6 substrate - 0.9048 90.48%
CYP3A4 inhibition + 0.5255 52.55%
CYP2C9 inhibition - 0.5447 54.47%
CYP2C19 inhibition + 0.7769 77.69%
CYP2D6 inhibition - 0.8077 80.77%
CYP1A2 inhibition + 0.8586 85.86%
CYP2C8 inhibition - 0.5590 55.90%
CYP inhibitory promiscuity + 0.6174 61.74%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6535 65.35%
Carcinogenicity (trinary) Non-required 0.7166 71.66%
Eye corrosion - 0.9717 97.17%
Eye irritation - 0.4786 47.86%
Skin irritation - 0.7249 72.49%
Skin corrosion - 0.9770 97.70%
Ames mutagenesis - 0.6278 62.78%
Human Ether-a-go-go-Related Gene inhibition - 0.3988 39.88%
Micronuclear - 0.6367 63.67%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation + 0.5593 55.93%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity + 0.5469 54.69%
Acute Oral Toxicity (c) III 0.5042 50.42%
Estrogen receptor binding - 0.5322 53.22%
Androgen receptor binding - 0.5418 54.18%
Thyroid receptor binding - 0.6154 61.54%
Glucocorticoid receptor binding - 0.5620 56.20%
Aromatase binding + 0.6470 64.70%
PPAR gamma - 0.6359 63.59%
Honey bee toxicity - 0.7951 79.51%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.6507 65.07%
Fish aquatic toxicity + 1.0000 100.00%

Targets

Top

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 94.58% 96.09%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 92.74% 97.21%
CHEMBL2581 P07339 Cathepsin D 91.72% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 91.20% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.79% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.70% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.24% 95.56%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.18% 96.95%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 86.03% 81.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.87% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.46% 94.45%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.10% 96.00%

Plants that contains it

Top
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.
Citrus aurantiifolia
Eupatorium cannabinum
Eupatorium fortunei
Lysimachia clethroides
Senna sophera

Cross-Links

Top
PubChem 10869933
NPASS NPC98748
ChEMBL CHEMBL1795991
LOTUS LTS0053008
wikiData Q27135891