(7E,13E)-pentadeca-7,13-dien-9,11-diyn-6-one

Details

Top
Internal ID 4fcd927b-ce8a-418c-af72-c823fd3400e3
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Alpha,beta-unsaturated ketones > Enones
IUPAC Name (7E,13E)-pentadeca-7,13-dien-9,11-diyn-6-one
SMILES (Canonical) CCCCCC(=O)C=CC#CC#CC=CC
SMILES (Isomeric) CCCCCC(=O)/C=C/C#CC#C/C=C/C
InChI InChI=1S/C15H18O/c1-3-5-7-8-9-10-12-14-15(16)13-11-6-4-2/h3,5,12,14H,4,6,11,13H2,1-2H3/b5-3+,14-12+
InChI Key FBYQVCKBMHGWKZ-AYYMJEHKSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H18O
Molecular Weight 214.30 g/mol
Exact Mass 214.135765193 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 4.10
Atomic LogP (AlogP) 3.27
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (7E,13E)-pentadeca-7,13-dien-9,11-diyn-6-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9931 99.31%
Caco-2 + 0.7731 77.31%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Plasma membrane 0.4186 41.86%
OATP2B1 inhibitior - 0.8584 85.84%
OATP1B1 inhibitior + 0.8543 85.43%
OATP1B3 inhibitior + 0.9325 93.25%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.7031 70.31%
P-glycoprotein inhibitior - 0.9469 94.69%
P-glycoprotein substrate - 0.8864 88.64%
CYP3A4 substrate - 0.5684 56.84%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8439 84.39%
CYP3A4 inhibition - 0.9416 94.16%
CYP2C9 inhibition - 0.9107 91.07%
CYP2C19 inhibition - 0.9016 90.16%
CYP2D6 inhibition - 0.9426 94.26%
CYP1A2 inhibition + 0.7891 78.91%
CYP2C8 inhibition - 0.8151 81.51%
CYP inhibitory promiscuity - 0.6476 64.76%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5600 56.00%
Carcinogenicity (trinary) Non-required 0.6725 67.25%
Eye corrosion + 0.8307 83.07%
Eye irritation - 0.7318 73.18%
Skin irritation + 0.8078 80.78%
Skin corrosion - 0.9230 92.30%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5056 50.56%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5548 55.48%
skin sensitisation + 0.9403 94.03%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity - 0.9889 98.89%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity + 0.5072 50.72%
Acute Oral Toxicity (c) III 0.7223 72.23%
Estrogen receptor binding - 0.7684 76.84%
Androgen receptor binding - 0.8489 84.89%
Thyroid receptor binding + 0.5180 51.80%
Glucocorticoid receptor binding - 0.6530 65.30%
Aromatase binding - 0.5577 55.77%
PPAR gamma - 0.6815 68.15%
Honey bee toxicity - 0.9701 97.01%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.6204 62.04%
Fish aquatic toxicity + 0.8722 87.22%

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
CHEMBL230 P35354 Cyclooxygenase-2 98.08% 89.63%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.91% 99.17%
CHEMBL2581 P07339 Cathepsin D 92.58% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.84% 96.09%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 87.59% 92.08%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 86.61% 91.81%
CHEMBL221 P23219 Cyclooxygenase-1 86.03% 90.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.79% 96.95%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 84.89% 92.86%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.56% 97.29%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 80.19% 85.94%

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.
Oenanthe aquatica

Cross-Links

Top
PubChem 101416444
LOTUS LTS0225740
wikiData Q104993013