(9E,15E)-heptadec-9,15-trien-11,13-diyn-4-one

Details

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Internal ID e94a5dba-8a27-44ab-85e6-088afac4588c
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Ketones
IUPAC Name (9E,15E)-heptadeca-9,15-dien-11,13-diyn-4-one
SMILES (Canonical) CCCC(=O)CCCCC=CC#CC#CC=CC
SMILES (Isomeric) CCCC(=O)CCCC/C=C/C#CC#C/C=C/C
InChI InChI=1S/C17H22O/c1-3-5-6-7-8-9-10-11-12-13-14-16-17(18)15-4-2/h3,5,10-11H,4,12-16H2,1-2H3/b5-3+,11-10+
InChI Key IIFDEYOLAIRRBS-SALZOXGJSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H22O
Molecular Weight 242.36 g/mol
Exact Mass 242.167065321 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 4.40
Atomic LogP (AlogP) 4.06
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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Heptadec-9E,15E-trien-11,13-diyn-4-one
CHEBI:187023
LMFA01060216
(9E,15E)-heptadeca-9,15-dien-11,13-diyn-4-one

2D Structure

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2D Structure of (9E,15E)-heptadec-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 + 0.8673 86.73%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Plasma membrane 0.5401 54.01%
OATP2B1 inhibitior - 0.8525 85.25%
OATP1B1 inhibitior + 0.7862 78.62%
OATP1B3 inhibitior + 0.9335 93.35%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.4625 46.25%
P-glycoprotein inhibitior - 0.9177 91.77%
P-glycoprotein substrate - 0.8462 84.62%
CYP3A4 substrate - 0.5431 54.31%
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 - 0.8572 85.72%
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 - 0.8393 83.93%
Skin irritation + 0.6148 61.48%
Skin corrosion - 0.9791 97.91%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6509 65.09%
Micronuclear - 0.9400 94.00%
Hepatotoxicity - 0.6125 61.25%
skin sensitisation + 0.9466 94.66%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity - 0.9111 91.11%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity - 0.6266 62.66%
Acute Oral Toxicity (c) III 0.7595 75.95%
Estrogen receptor binding - 0.8073 80.73%
Androgen receptor binding - 0.8290 82.90%
Thyroid receptor binding + 0.5648 56.48%
Glucocorticoid receptor binding - 0.6399 63.99%
Aromatase binding - 0.6228 62.28%
PPAR gamma - 0.5146 51.46%
Honey bee toxicity - 0.9384 93.84%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5400 54.00%
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 94.42% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.00% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.47% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.91% 91.11%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 81.36% 85.94%
CHEMBL221 P23219 Cyclooxygenase-1 81.33% 90.17%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 81.21% 92.08%

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 134812115
LOTUS LTS0254200
wikiData Q105113438