N-(2-oxotrideca-9,11-dienyl)acetamide

Details

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Internal ID be4050b6-8623-4ae2-9b8f-81e0b806a522
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Carboxylic acid derivatives > Carboxylic acid amides > Acetamides
IUPAC Name N-(2-oxotrideca-9,11-dienyl)acetamide
SMILES (Canonical) CC=CC=CCCCCCCC(=O)CNC(=O)C
SMILES (Isomeric) CC=CC=CCCCCCCC(=O)CNC(=O)C
InChI InChI=1S/C15H25NO2/c1-3-4-5-6-7-8-9-10-11-12-15(18)13-16-14(2)17/h3-6H,7-13H2,1-2H3,(H,16,17)
InChI Key HVQRHJSURJCJCC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H25NO2
Molecular Weight 251.36 g/mol
Exact Mass 251.188529040 g/mol
Topological Polar Surface Area (TPSA) 46.20 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.16
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of N-(2-oxotrideca-9,11-dienyl)acetamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9768 97.68%
Caco-2 + 0.7551 75.51%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.8036 80.36%
OATP2B1 inhibitior - 0.8536 85.36%
OATP1B1 inhibitior + 0.8522 85.22%
OATP1B3 inhibitior + 0.9439 94.39%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.6585 65.85%
P-glycoprotein inhibitior - 0.8168 81.68%
P-glycoprotein substrate - 0.7593 75.93%
CYP3A4 substrate - 0.5563 55.63%
CYP2C9 substrate - 0.6194 61.94%
CYP2D6 substrate - 0.8578 85.78%
CYP3A4 inhibition - 0.9485 94.85%
CYP2C9 inhibition - 0.7861 78.61%
CYP2C19 inhibition - 0.7255 72.55%
CYP2D6 inhibition - 0.9259 92.59%
CYP1A2 inhibition - 0.6528 65.28%
CYP2C8 inhibition - 0.9384 93.84%
CYP inhibitory promiscuity - 0.7440 74.40%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Non-required 0.6864 68.64%
Eye corrosion - 0.9008 90.08%
Eye irritation - 0.8763 87.63%
Skin irritation - 0.7931 79.31%
Skin corrosion - 0.9473 94.73%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7856 78.56%
Micronuclear - 0.7800 78.00%
Hepatotoxicity - 0.5092 50.92%
skin sensitisation - 0.9118 91.18%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity - 0.7941 79.41%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.7671 76.71%
Estrogen receptor binding - 0.7440 74.40%
Androgen receptor binding - 0.7827 78.27%
Thyroid receptor binding + 0.5898 58.98%
Glucocorticoid receptor binding - 0.7584 75.84%
Aromatase binding - 0.7260 72.60%
PPAR gamma - 0.5348 53.48%
Honey bee toxicity - 0.9423 94.23%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity - 0.6782 67.82%

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
CHEMBL4040 P28482 MAP kinase ERK2 96.30% 83.82%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.14% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.62% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.52% 91.11%
CHEMBL1829 O15379 Histone deacetylase 3 91.60% 95.00%
CHEMBL2581 P07339 Cathepsin D 90.79% 98.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 87.07% 97.21%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.27% 96.95%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 84.30% 94.33%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 83.85% 97.29%
CHEMBL3401 O75469 Pregnane X receptor 81.64% 94.73%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 163064998
LOTUS LTS0007853
wikiData Q104168440