Pentadeca-8,13-dien-11-YN-2-one

Details

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Internal ID c5843542-3745-4797-b92f-6974135bb9cf
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Ketones
IUPAC Name pentadeca-8,13-dien-11-yn-2-one
SMILES (Canonical) CC=CC#CCC=CCCCCCC(=O)C
SMILES (Isomeric) CC=CC#CCC=CCCCCCC(=O)C
InChI InChI=1S/C15H22O/c1-3-4-5-6-7-8-9-10-11-12-13-14-15(2)16/h3-4,8-9H,7,10-14H2,1-2H3
InChI Key MTRMYFQVGGDQQK-UHFFFAOYSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O
Molecular Weight 218.33 g/mol
Exact Mass 218.167065321 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 4.00
Atomic LogP (AlogP) 4.05
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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DTXSID60766973

2D Structure

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2D Structure of Pentadeca-8,13-dien-11-YN-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9916 99.16%
Caco-2 + 0.9313 93.13%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Plasma membrane 0.3575 35.75%
OATP2B1 inhibitior - 0.8554 85.54%
OATP1B1 inhibitior + 0.8350 83.50%
OATP1B3 inhibitior + 0.9316 93.16%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.7630 76.30%
P-glycoprotein inhibitior - 0.9368 93.68%
P-glycoprotein substrate - 0.8922 89.22%
CYP3A4 substrate - 0.5398 53.98%
CYP2C9 substrate - 0.8070 80.70%
CYP2D6 substrate - 0.8174 81.74%
CYP3A4 inhibition - 0.9530 95.30%
CYP2C9 inhibition - 0.9181 91.81%
CYP2C19 inhibition - 0.9287 92.87%
CYP2D6 inhibition - 0.9598 95.98%
CYP1A2 inhibition + 0.6948 69.48%
CYP2C8 inhibition - 0.8783 87.83%
CYP inhibitory promiscuity - 0.7828 78.28%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5400 54.00%
Carcinogenicity (trinary) Non-required 0.7102 71.02%
Eye corrosion + 0.8910 89.10%
Eye irritation - 0.7476 74.76%
Skin irritation + 0.7677 76.77%
Skin corrosion - 0.9401 94.01%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7261 72.61%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5342 53.42%
skin sensitisation + 0.9468 94.68%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.9719 97.19%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity + 0.5868 58.68%
Acute Oral Toxicity (c) III 0.8326 83.26%
Estrogen receptor binding - 0.7657 76.57%
Androgen receptor binding - 0.9210 92.10%
Thyroid receptor binding - 0.5350 53.50%
Glucocorticoid receptor binding - 0.5811 58.11%
Aromatase binding - 0.7276 72.76%
PPAR gamma + 0.5385 53.85%
Honey bee toxicity - 0.9244 92.44%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity + 0.6524 65.24%
Fish aquatic toxicity + 0.9069 90.69%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 96.28% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.22% 96.09%
CHEMBL2581 P07339 Cathepsin D 90.94% 98.95%
CHEMBL1829 O15379 Histone deacetylase 3 84.92% 95.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.49% 96.00%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.99% 97.21%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.88% 94.33%

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.
Echinacea pallida

Cross-Links

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PubChem 71339566
LOTUS LTS0119985
wikiData Q105171834