Tetradeca-8-en-11,13-diyn-2-one

Details

Top
Internal ID eaafdc11-6eb8-4a10-8972-4ae7eef18b28
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Ketones
IUPAC Name tetradec-8-en-11,13-diyn-2-one
SMILES (Canonical) CC(=O)CCCCCC=CCC#CC#C
SMILES (Isomeric) CC(=O)CCCCCC=CCC#CC#C
InChI InChI=1S/C14H18O/c1-3-4-5-6-7-8-9-10-11-12-13-14(2)15/h1,7-8H,6,9-13H2,2H3
InChI Key OUTVNYVJKIBGGD-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

Top
Molecular Formula C14H18O
Molecular Weight 202.29 g/mol
Exact Mass 202.135765193 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.11
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Tetradeca-8-en-11,13-diyn-2-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9918 99.18%
Caco-2 + 0.9312 93.12%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Plasma membrane 0.4638 46.38%
OATP2B1 inhibitior - 0.8546 85.46%
OATP1B1 inhibitior + 0.8748 87.48%
OATP1B3 inhibitior + 0.9243 92.43%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.6299 62.99%
P-glycoprotein inhibitior - 0.9649 96.49%
P-glycoprotein substrate - 0.8949 89.49%
CYP3A4 substrate - 0.5446 54.46%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8077 80.77%
CYP3A4 inhibition - 0.9687 96.87%
CYP2C9 inhibition - 0.9112 91.12%
CYP2C19 inhibition - 0.9182 91.82%
CYP2D6 inhibition - 0.9666 96.66%
CYP1A2 inhibition + 0.7653 76.53%
CYP2C8 inhibition - 0.8746 87.46%
CYP inhibitory promiscuity - 0.7533 75.33%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5400 54.00%
Carcinogenicity (trinary) Non-required 0.6606 66.06%
Eye corrosion + 0.9336 93.36%
Eye irritation - 0.7893 78.93%
Skin irritation + 0.8524 85.24%
Skin corrosion - 0.8593 85.93%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4871 48.71%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5717 57.17%
skin sensitisation + 0.9112 91.12%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.9785 97.85%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.4886 48.86%
Acute Oral Toxicity (c) III 0.7350 73.50%
Estrogen receptor binding - 0.8308 83.08%
Androgen receptor binding - 0.9205 92.05%
Thyroid receptor binding - 0.6991 69.91%
Glucocorticoid receptor binding - 0.4844 48.44%
Aromatase binding - 0.6312 63.12%
PPAR gamma + 0.5678 56.78%
Honey bee toxicity - 0.9442 94.42%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity + 0.6924 69.24%
Fish aquatic toxicity + 0.8981 89.81%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 96.28% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.68% 96.09%
CHEMBL230 P35354 Cyclooxygenase-2 90.72% 89.63%
CHEMBL2581 P07339 Cathepsin D 89.74% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.33% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.19% 91.11%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 83.39% 89.34%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 81.29% 96.09%
CHEMBL1829 O15379 Histone deacetylase 3 80.18% 95.00%

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.
Centaurea pullata
Echinacea pallida

Cross-Links

Top
PubChem 72996063
LOTUS LTS0255188
wikiData Q105200425