Heptadeca-1,8,16-trien-4,6-diyn-3-one

Details

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Internal ID 0ec5ac52-6e88-429a-839c-f4f8dd27dd8b
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Alpha,beta-unsaturated ketones > Enones
IUPAC Name heptadeca-1,8,16-trien-4,6-diyn-3-one
SMILES (Canonical) C=CCCCCCCC=CC#CC#CC(=O)C=C
SMILES (Isomeric) C=CCCCCCCC=CC#CC#CC(=O)C=C
InChI InChI=1S/C17H20O/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17(18)4-2/h3-4,11-12H,1-2,5-10H2
InChI Key SDLHNQGTGGNOQZ-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 5.70
Atomic LogP (AlogP) 3.83
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Heptadeca-1,8,16-trien-4,6-diyn-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 + 0.9861 98.61%
Caco-2 + 0.6046 60.46%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Plasma membrane 0.4702 47.02%
OATP2B1 inhibitior - 0.8602 86.02%
OATP1B1 inhibitior + 0.8780 87.80%
OATP1B3 inhibitior + 0.9454 94.54%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8417 84.17%
P-glycoprotein inhibitior - 0.9101 91.01%
P-glycoprotein substrate - 0.8485 84.85%
CYP3A4 substrate - 0.5098 50.98%
CYP2C9 substrate - 0.6126 61.26%
CYP2D6 substrate - 0.8026 80.26%
CYP3A4 inhibition - 0.9494 94.94%
CYP2C9 inhibition - 0.8131 81.31%
CYP2C19 inhibition - 0.8354 83.54%
CYP2D6 inhibition - 0.9646 96.46%
CYP1A2 inhibition + 0.5199 51.99%
CYP2C8 inhibition - 0.8203 82.03%
CYP inhibitory promiscuity - 0.6046 60.46%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5200 52.00%
Carcinogenicity (trinary) Non-required 0.5899 58.99%
Eye corrosion + 0.9781 97.81%
Eye irritation - 0.5954 59.54%
Skin irritation + 0.7063 70.63%
Skin corrosion - 0.7446 74.46%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6600 66.00%
Micronuclear - 0.9400 94.00%
Hepatotoxicity - 0.6322 63.22%
skin sensitisation + 0.8298 82.98%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.9222 92.22%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity + 0.6655 66.55%
Acute Oral Toxicity (c) III 0.3863 38.63%
Estrogen receptor binding - 0.5000 50.00%
Androgen receptor binding - 0.5653 56.53%
Thyroid receptor binding + 0.5155 51.55%
Glucocorticoid receptor binding + 0.6604 66.04%
Aromatase binding - 0.6148 61.48%
PPAR gamma + 0.7599 75.99%
Honey bee toxicity - 0.7892 78.92%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5762 57.62%
Fish aquatic toxicity + 0.8553 85.53%

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 91.22% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 89.99% 96.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.43% 96.09%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 87.90% 89.34%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 87.69% 95.17%
CHEMBL4246 P42680 Tyrosine-protein kinase TEC 86.27% 82.05%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.46% 91.11%
CHEMBL1829 O15379 Histone deacetylase 3 84.69% 95.00%
CHEMBL5251 Q06187 Tyrosine-protein kinase BTK 84.09% 98.51%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 83.74% 97.21%
CHEMBL221 P23219 Cyclooxygenase-1 81.41% 90.17%

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 162981330
LOTUS LTS0066560
wikiData Q105250719