Heptadeca-1,4,8,10,16-pentaen-6-yn-3-one

Details

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Internal ID 1b519d6b-4c85-4bc3-80e1-71275f4eb63f
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Alpha,beta-unsaturated ketones > Enones
IUPAC Name heptadeca-1,4,8,10,16-pentaen-6-yn-3-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H20O/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17(18)4-2/h3-4,9-12,15-16H,1-2,5-8H2
InChI Key JGTUTFWHNIOOOC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H20O
Molecular Weight 240.34 g/mol
Exact Mass 240.151415257 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 5.10
Atomic LogP (AlogP) 4.16
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 8

Synonyms

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29739-56-8
DTXSID10781535

2D Structure

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2D Structure of Heptadeca-1,4,8,10,16-pentaen-6-yn-3-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9833 98.33%
Caco-2 + 0.6932 69.32%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Plasma membrane 0.4067 40.67%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8827 88.27%
OATP1B3 inhibitior + 0.9482 94.82%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.7779 77.79%
P-glycoprotein inhibitior - 0.8694 86.94%
P-glycoprotein substrate - 0.9235 92.35%
CYP3A4 substrate - 0.5289 52.89%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8201 82.01%
CYP3A4 inhibition - 0.9311 93.11%
CYP2C9 inhibition - 0.8392 83.92%
CYP2C19 inhibition - 0.8148 81.48%
CYP2D6 inhibition - 0.9637 96.37%
CYP1A2 inhibition + 0.5427 54.27%
CYP2C8 inhibition - 0.8210 82.10%
CYP inhibitory promiscuity - 0.5613 56.13%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5300 53.00%
Carcinogenicity (trinary) Non-required 0.5178 51.78%
Eye corrosion + 0.9830 98.30%
Eye irritation - 0.4845 48.45%
Skin irritation + 0.7697 76.97%
Skin corrosion - 0.5313 53.13%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4221 42.21%
Micronuclear - 0.8900 89.00%
Hepatotoxicity - 0.5500 55.00%
skin sensitisation + 0.8409 84.09%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity - 0.8889 88.89%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.6123 61.23%
Acute Oral Toxicity (c) II 0.3591 35.91%
Estrogen receptor binding + 0.6782 67.82%
Androgen receptor binding - 0.6787 67.87%
Thyroid receptor binding + 0.6580 65.80%
Glucocorticoid receptor binding + 0.6808 68.08%
Aromatase binding - 0.4950 49.50%
PPAR gamma + 0.8121 81.21%
Honey bee toxicity - 0.7700 77.00%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.7267 72.67%

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 88.51% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.10% 96.09%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 85.94% 89.34%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.56% 96.95%
CHEMBL4246 P42680 Tyrosine-protein kinase TEC 83.51% 82.05%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.07% 91.11%
CHEMBL279 P35968 Vascular endothelial growth factor receptor 2 81.19% 95.52%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.49% 94.45%

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.
Tridax trilobata

Cross-Links

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PubChem 71357462
LOTUS LTS0238111
wikiData Q82745490