Methyl 2-hexa-2,4-diynoyl-6-methoxybenzoate

Details

Top
Internal ID ac20ec8c-12f1-4123-a49d-95eb911947b4
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Methoxybenzoic acids and derivatives > O-methoxybenzoic acids and derivatives
IUPAC Name methyl 2-hexa-2,4-diynoyl-6-methoxybenzoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H12O4/c1-4-5-6-9-12(16)11-8-7-10-13(18-2)14(11)15(17)19-3/h7-8,10H,1-3H3
InChI Key WPJOSCVCQRPYNJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H12O4
Molecular Weight 256.25 g/mol
Exact Mass 256.07355886 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 2.80
Atomic LogP (AlogP) 1.69
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Methyl 2-hexa-2,4-diynoyl-6-methoxybenzoate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9859 98.59%
Caco-2 + 0.5118 51.18%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.8753 87.53%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9539 95.39%
OATP1B3 inhibitior + 0.9638 96.38%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8149 81.49%
P-glycoprotein inhibitior - 0.8321 83.21%
P-glycoprotein substrate - 0.6959 69.59%
CYP3A4 substrate + 0.5174 51.74%
CYP2C9 substrate - 0.8055 80.55%
CYP2D6 substrate - 0.8263 82.63%
CYP3A4 inhibition - 0.7867 78.67%
CYP2C9 inhibition - 0.9615 96.15%
CYP2C19 inhibition - 0.9295 92.95%
CYP2D6 inhibition - 0.9606 96.06%
CYP1A2 inhibition + 0.5621 56.21%
CYP2C8 inhibition + 0.4536 45.36%
CYP inhibitory promiscuity - 0.7899 78.99%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6079 60.79%
Carcinogenicity (trinary) Non-required 0.6818 68.18%
Eye corrosion - 0.6094 60.94%
Eye irritation + 0.5249 52.49%
Skin irritation - 0.7646 76.46%
Skin corrosion - 0.9182 91.82%
Ames mutagenesis - 0.6454 64.54%
Human Ether-a-go-go-Related Gene inhibition - 0.5396 53.96%
Micronuclear + 0.5207 52.07%
Hepatotoxicity + 0.5703 57.03%
skin sensitisation - 0.9361 93.61%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity + 0.7281 72.81%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.8164 81.64%
Acute Oral Toxicity (c) II 0.6302 63.02%
Estrogen receptor binding + 0.7575 75.75%
Androgen receptor binding + 0.5929 59.29%
Thyroid receptor binding - 0.4936 49.36%
Glucocorticoid receptor binding - 0.4698 46.98%
Aromatase binding + 0.5924 59.24%
PPAR gamma - 0.7283 72.83%
Honey bee toxicity - 0.9381 93.81%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.9760 97.60%

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 96.28% 96.09%
CHEMBL2535 P11166 Glucose transporter 93.90% 98.75%
CHEMBL1255126 O15151 Protein Mdm4 92.71% 90.20%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 90.71% 95.50%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.17% 86.33%
CHEMBL221 P23219 Cyclooxygenase-1 88.00% 90.17%
CHEMBL2581 P07339 Cathepsin D 87.02% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.32% 96.00%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 84.42% 81.11%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.57% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.32% 99.23%
CHEMBL5028 O14672 ADAM10 80.08% 97.50%

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.
Argyranthemum frutescens

Cross-Links

Top
PubChem 162895572
LOTUS LTS0089586
wikiData Q105309992