12-Pyridin-3-yldodeca-4,6-dien-2-yl acetate

Details

Top
Internal ID 1eda68d4-5e04-4e46-b71f-f7e9237d9af4
Taxonomy Organoheterocyclic compounds > Pyridines and derivatives
IUPAC Name 12-pyridin-3-yldodeca-4,6-dien-2-yl acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H27NO2/c1-17(22-18(2)21)12-9-7-5-3-4-6-8-10-13-19-14-11-15-20-16-19/h3,5,7,9,11,14-17H,4,6,8,10,12-13H2,1-2H3
InChI Key XTROEZZUUMAJED-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C19H27NO2
Molecular Weight 301.40 g/mol
Exact Mass 301.204179104 g/mol
Topological Polar Surface Area (TPSA) 39.20 Ų
XlogP 4.90
Atomic LogP (AlogP) 4.64
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 10

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 12-Pyridin-3-yldodeca-4,6-dien-2-yl acetate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9954 99.54%
Caco-2 + 0.6007 60.07%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Plasma membrane 0.5314 53.14%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8903 89.03%
OATP1B3 inhibitior + 0.9308 93.08%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.8959 89.59%
P-glycoprotein inhibitior - 0.7242 72.42%
P-glycoprotein substrate - 0.7235 72.35%
CYP3A4 substrate + 0.5353 53.53%
CYP2C9 substrate - 0.6171 61.71%
CYP2D6 substrate - 0.8738 87.38%
CYP3A4 inhibition - 0.5910 59.10%
CYP2C9 inhibition - 0.6848 68.48%
CYP2C19 inhibition - 0.6131 61.31%
CYP2D6 inhibition - 0.8384 83.84%
CYP1A2 inhibition + 0.5161 51.61%
CYP2C8 inhibition + 0.4863 48.63%
CYP inhibitory promiscuity + 0.5648 56.48%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7728 77.28%
Carcinogenicity (trinary) Non-required 0.6057 60.57%
Eye corrosion - 0.8863 88.63%
Eye irritation - 0.9387 93.87%
Skin irritation - 0.6359 63.59%
Skin corrosion - 0.9824 98.24%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7517 75.17%
Micronuclear - 0.9000 90.00%
Hepatotoxicity - 0.5217 52.17%
skin sensitisation - 0.5292 52.92%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity - 0.6145 61.45%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity - 0.7245 72.45%
Acute Oral Toxicity (c) III 0.7345 73.45%
Estrogen receptor binding - 0.4754 47.54%
Androgen receptor binding - 0.7110 71.10%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding - 0.4864 48.64%
Aromatase binding - 0.6024 60.24%
PPAR gamma + 0.5255 52.55%
Honey bee toxicity - 0.8944 89.44%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5437 54.37%
Fish aquatic toxicity + 0.6861 68.61%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.67% 94.45%
CHEMBL2581 P07339 Cathepsin D 98.19% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.04% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.19% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 92.29% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.13% 91.11%
CHEMBL3975 P09467 Fructose-1,6-bisphosphatase 89.06% 92.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 88.73% 89.34%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.63% 86.33%
CHEMBL255 P29275 Adenosine A2b receptor 87.26% 98.59%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.19% 95.50%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.24% 96.00%
CHEMBL240 Q12809 HERG 80.90% 89.76%
CHEMBL1781 P11387 DNA topoisomerase I 80.13% 97.00%

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.
There are no matching plants.

Cross-Links

Top
PubChem 73825925
LOTUS LTS0180271
wikiData Q105341819