Methyl 2-(1-acetyloxypenta-2,4-diynyl)benzoate

Details

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Internal ID a8a3ac07-2788-4fe3-b285-666632ea0e02
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Benzoic acid esters
IUPAC Name methyl 2-(1-acetyloxypenta-2,4-diynyl)benzoate
SMILES (Canonical) CC(=O)OC(C#CC#C)C1=CC=CC=C1C(=O)OC
SMILES (Isomeric) CC(=O)OC(C#CC#C)C1=CC=CC=C1C(=O)OC
InChI InChI=1S/C15H12O4/c1-4-5-10-14(19-11(2)16)12-8-6-7-9-13(12)15(17)18-3/h1,6-9,14H,2-3H3
InChI Key HZESUMDEVRGUII-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H12O4
Molecular Weight 256.25 g/mol
Exact Mass 256.07355886 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 2.20
Atomic LogP (AlogP) 1.71
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Methyl 2-(1-acetyloxypenta-2,4-diynyl)benzoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9744 97.44%
Caco-2 - 0.6373 63.73%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.9140 91.40%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9428 94.28%
OATP1B3 inhibitior + 0.9743 97.43%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.6609 66.09%
P-glycoprotein inhibitior - 0.9092 90.92%
P-glycoprotein substrate - 0.8444 84.44%
CYP3A4 substrate + 0.5229 52.29%
CYP2C9 substrate - 0.7571 75.71%
CYP2D6 substrate - 0.8867 88.67%
CYP3A4 inhibition - 0.8716 87.16%
CYP2C9 inhibition - 0.8915 89.15%
CYP2C19 inhibition - 0.8437 84.37%
CYP2D6 inhibition - 0.9609 96.09%
CYP1A2 inhibition - 0.6115 61.15%
CYP2C8 inhibition - 0.6484 64.84%
CYP inhibitory promiscuity - 0.6628 66.28%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5385 53.85%
Carcinogenicity (trinary) Non-required 0.7227 72.27%
Eye corrosion + 0.5000 50.00%
Eye irritation - 0.7500 75.00%
Skin irritation - 0.7258 72.58%
Skin corrosion - 0.9561 95.61%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5661 56.61%
Micronuclear - 0.7326 73.26%
Hepatotoxicity - 0.5588 55.88%
skin sensitisation - 0.6479 64.79%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.5889 58.89%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity + 0.6715 67.15%
Acute Oral Toxicity (c) III 0.4662 46.62%
Estrogen receptor binding + 0.6179 61.79%
Androgen receptor binding - 0.7059 70.59%
Thyroid receptor binding - 0.5580 55.80%
Glucocorticoid receptor binding + 0.6453 64.53%
Aromatase binding - 0.5652 56.52%
PPAR gamma - 0.5505 55.05%
Honey bee toxicity - 0.7562 75.62%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9670 96.70%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.57% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.76% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.35% 96.09%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 89.66% 95.50%
CHEMBL3401 O75469 Pregnane X receptor 87.78% 94.73%
CHEMBL2535 P11166 Glucose transporter 86.92% 98.75%
CHEMBL221 P23219 Cyclooxygenase-1 85.02% 90.17%
CHEMBL2321614 Q9NPC2 Potassium channel subfamily K member 9 84.87% 80.00%
CHEMBL5028 O14672 ADAM10 82.76% 97.50%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.21% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.04% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.96% 94.45%

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.
Ismelia carinata

Cross-Links

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PubChem 162946761
LOTUS LTS0006022
wikiData Q105110669