7-(3-Hydroxyphenyl)hept-2-en-4,6-diynyl acetate

Details

Top
Internal ID 7ca64c53-6701-454d-8bd7-48dfd9fc2fbb
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohol esters
IUPAC Name 7-(3-hydroxyphenyl)hept-2-en-4,6-diynyl acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H12O3/c1-13(16)18-11-6-4-2-3-5-8-14-9-7-10-15(17)12-14/h4,6-7,9-10,12,17H,11H2,1H3
InChI Key MMOVXOSWCFTDFC-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H12O3
Molecular Weight 240.25 g/mol
Exact Mass 240.078644241 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 2.70
Atomic LogP (AlogP) 1.87
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 7-(3-Hydroxyphenyl)hept-2-en-4,6-diynyl acetate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 - 0.7174 71.74%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.8954 89.54%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8740 87.40%
OATP1B3 inhibitior + 0.9634 96.34%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.6837 68.37%
P-glycoprotein inhibitior - 0.9057 90.57%
P-glycoprotein substrate - 0.8447 84.47%
CYP3A4 substrate + 0.5399 53.99%
CYP2C9 substrate + 0.6049 60.49%
CYP2D6 substrate - 0.8556 85.56%
CYP3A4 inhibition - 0.8249 82.49%
CYP2C9 inhibition - 0.9326 93.26%
CYP2C19 inhibition - 0.8031 80.31%
CYP2D6 inhibition - 0.9434 94.34%
CYP1A2 inhibition + 0.6023 60.23%
CYP2C8 inhibition + 0.5164 51.64%
CYP inhibitory promiscuity - 0.7222 72.22%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6457 64.57%
Carcinogenicity (trinary) Non-required 0.6831 68.31%
Eye corrosion - 0.8956 89.56%
Eye irritation - 0.6305 63.05%
Skin irritation + 0.6577 65.77%
Skin corrosion - 0.8792 87.92%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6868 68.68%
Micronuclear - 0.7571 75.71%
Hepatotoxicity - 0.5048 50.48%
skin sensitisation - 0.5639 56.39%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.8333 83.33%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.4844 48.44%
Acute Oral Toxicity (c) III 0.7175 71.75%
Estrogen receptor binding + 0.8224 82.24%
Androgen receptor binding - 0.5872 58.72%
Thyroid receptor binding - 0.4938 49.38%
Glucocorticoid receptor binding - 0.5422 54.22%
Aromatase binding + 0.7220 72.20%
PPAR gamma + 0.5539 55.39%
Honey bee toxicity - 0.9087 90.87%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.5155 51.55%
Fish aquatic toxicity + 0.9797 97.97%

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 95.60% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.94% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.61% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.22% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 91.14% 94.73%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 90.70% 96.42%
CHEMBL2581 P07339 Cathepsin D 90.35% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.33% 95.56%
CHEMBL2535 P11166 Glucose transporter 86.18% 98.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.90% 96.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.96% 94.45%

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.
Carlina diae
Carlina vulgaris

Cross-Links

Top
PubChem 162957247
LOTUS LTS0011208
wikiData Q105167943