7-phenylhept-2-en-4,6-diynyl Acetate

Details

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Internal ID f6025d8f-70dd-4bd5-b3ad-f74ae3dfff1f
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohol esters
IUPAC Name 7-phenylhept-2-en-4,6-diynyl acetate
SMILES (Canonical) CC(=O)OCC=CC#CC#CC1=CC=CC=C1
SMILES (Isomeric) CC(=O)OCC=CC#CC#CC1=CC=CC=C1
InChI InChI=1S/C15H12O2/c1-14(16)17-13-9-4-2-3-6-10-15-11-7-5-8-12-15/h4-5,7-9,11-12H,13H2,1H3
InChI Key JEAKICNMCJBNSA-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H12O2
Molecular Weight 224.25 g/mol
Exact Mass 224.083729621 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.16
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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7-phenylhept-2-en-4,6-diynyl Acetate
DTXSID80942373
7-phenylhept-2-ene-4,6-diyn-1-yl acetate
2-Heptene-4,6-diyn-1-ol, 7-phenyl-, acetate

2D Structure

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2D Structure of 7-phenylhept-2-en-4,6-diynyl Acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 - 0.6006 60.06%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.6539 65.39%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8980 89.80%
OATP1B3 inhibitior + 0.9556 95.56%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.5990 59.90%
P-glycoprotein inhibitior - 0.9389 93.89%
P-glycoprotein substrate - 0.9548 95.48%
CYP3A4 substrate - 0.5654 56.54%
CYP2C9 substrate + 0.6055 60.55%
CYP2D6 substrate - 0.8646 86.46%
CYP3A4 inhibition - 0.9265 92.65%
CYP2C9 inhibition - 0.8669 86.69%
CYP2C19 inhibition - 0.8016 80.16%
CYP2D6 inhibition - 0.9429 94.29%
CYP1A2 inhibition + 0.7789 77.89%
CYP2C8 inhibition - 0.7474 74.74%
CYP inhibitory promiscuity - 0.5699 56.99%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5584 55.84%
Carcinogenicity (trinary) Non-required 0.7091 70.91%
Eye corrosion + 0.6626 66.26%
Eye irritation + 0.6000 60.00%
Skin irritation + 0.8759 87.59%
Skin corrosion - 0.7680 76.80%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6583 65.83%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.5606 56.06%
skin sensitisation + 0.8253 82.53%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity - 0.7889 78.89%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity + 0.6813 68.13%
Acute Oral Toxicity (c) III 0.7933 79.33%
Estrogen receptor binding + 0.7748 77.48%
Androgen receptor binding - 0.5785 57.85%
Thyroid receptor binding - 0.6194 61.94%
Glucocorticoid receptor binding + 0.5511 55.11%
Aromatase binding + 0.6955 69.55%
PPAR gamma - 0.5672 56.72%
Honey bee toxicity - 0.9325 93.25%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.5555 55.55%
Fish aquatic toxicity + 0.9840 98.40%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.41% 96.09%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 93.45% 94.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.25% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.38% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.32% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.96% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 86.88% 94.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.32% 96.00%
CHEMBL2581 P07339 Cathepsin D 85.08% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 84.37% 90.17%
CHEMBL5028 O14672 ADAM10 81.72% 97.50%

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.
Coreopsis grandiflora
Coreopsis nuecensis
Dahlia australis

Cross-Links

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PubChem 89297
LOTUS LTS0043301
wikiData Q82919369