Heptadeca-7,9,15-trien-11,13-diyn-4-one

Details

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Internal ID fa4babab-f9c0-48c6-a294-5f2cb5831616
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Ketones
IUPAC Name heptadeca-7,9,15-trien-11,13-diyn-4-one
SMILES (Canonical) CCCC(=O)CCC=CC=CC#CC#CC=CC
SMILES (Isomeric) CCCC(=O)CCC=CC=CC#CC#CC=CC
InChI InChI=1S/C17H20O/c1-3-5-6-7-8-9-10-11-12-13-14-16-17(18)15-4-2/h3,5,10-13H,4,14-16H2,1-2H3
InChI Key JRTSGUNUURZHCS-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 4.10
Atomic LogP (AlogP) 3.83
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Heptadeca-7,9,15-trien-11,13-diyn-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9921 99.21%
Caco-2 + 0.8675 86.75%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Plasma membrane 0.5401 54.01%
OATP2B1 inhibitior - 0.8557 85.57%
OATP1B1 inhibitior + 0.8155 81.55%
OATP1B3 inhibitior + 0.9335 93.35%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.4783 47.83%
P-glycoprotein inhibitior - 0.9457 94.57%
P-glycoprotein substrate - 0.8530 85.30%
CYP3A4 substrate - 0.5299 52.99%
CYP2C9 substrate - 0.8070 80.70%
CYP2D6 substrate - 0.8174 81.74%
CYP3A4 inhibition - 0.9457 94.57%
CYP2C9 inhibition - 0.9013 90.13%
CYP2C19 inhibition - 0.9225 92.25%
CYP2D6 inhibition - 0.9486 94.86%
CYP1A2 inhibition + 0.7025 70.25%
CYP2C8 inhibition - 0.8608 86.08%
CYP inhibitory promiscuity - 0.6554 65.54%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5500 55.00%
Carcinogenicity (trinary) Non-required 0.6509 65.09%
Eye corrosion + 0.8386 83.86%
Eye irritation - 0.8566 85.66%
Skin irritation + 0.6148 61.48%
Skin corrosion - 0.9791 97.91%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6993 69.93%
Micronuclear - 0.9400 94.00%
Hepatotoxicity - 0.5500 55.00%
skin sensitisation + 0.9466 94.66%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity - 0.9111 91.11%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity + 0.5830 58.30%
Acute Oral Toxicity (c) III 0.7595 75.95%
Estrogen receptor binding - 0.7292 72.92%
Androgen receptor binding - 0.7403 74.03%
Thyroid receptor binding - 0.5395 53.95%
Glucocorticoid receptor binding - 0.5692 56.92%
Aromatase binding + 0.5309 53.09%
PPAR gamma + 0.5368 53.68%
Honey bee toxicity - 0.9316 93.16%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.8728 87.28%

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 89.72% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.07% 96.09%
CHEMBL2581 P07339 Cathepsin D 85.71% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 84.72% 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.
Oenanthe crocata

Cross-Links

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PubChem 163085784
LOTUS LTS0021443
wikiData Q105134104