N-(2-phenylethyl)deca-2,8-dien-6-ynamide

Details

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Internal ID a2fd7ab5-f825-415e-840d-99d1e28384ba
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty amides > N-acyl amines
IUPAC Name N-(2-phenylethyl)deca-2,8-dien-6-ynamide
SMILES (Canonical) CC=CC#CCCC=CC(=O)NCCC1=CC=CC=C1
SMILES (Isomeric) CC=CC#CCCC=CC(=O)NCCC1=CC=CC=C1
InChI InChI=1S/C18H21NO/c1-2-3-4-5-6-7-11-14-18(20)19-16-15-17-12-9-8-10-13-17/h2-3,8-14H,6-7,15-16H2,1H3,(H,19,20)
InChI Key ARURMHBBHGPVCD-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H21NO
Molecular Weight 267.40 g/mol
Exact Mass 267.162314293 g/mol
Topological Polar Surface Area (TPSA) 29.10 Ų
XlogP 3.90
Atomic LogP (AlogP) 3.26
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of N-(2-phenylethyl)deca-2,8-dien-6-ynamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9930 99.30%
Caco-2 + 0.6419 64.19%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Lysosomes 0.4357 43.57%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8219 82.19%
OATP1B3 inhibitior + 0.9523 95.23%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.5950 59.50%
P-glycoprotein inhibitior - 0.7957 79.57%
P-glycoprotein substrate - 0.5336 53.36%
CYP3A4 substrate + 0.5373 53.73%
CYP2C9 substrate - 0.7958 79.58%
CYP2D6 substrate - 0.8692 86.92%
CYP3A4 inhibition - 0.7771 77.71%
CYP2C9 inhibition - 0.6677 66.77%
CYP2C19 inhibition + 0.5789 57.89%
CYP2D6 inhibition - 0.9328 93.28%
CYP1A2 inhibition + 0.7608 76.08%
CYP2C8 inhibition + 0.6476 64.76%
CYP inhibitory promiscuity + 0.5273 52.73%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7400 74.00%
Carcinogenicity (trinary) Non-required 0.6593 65.93%
Eye corrosion - 0.8809 88.09%
Eye irritation - 0.9731 97.31%
Skin irritation - 0.6921 69.21%
Skin corrosion - 0.8870 88.70%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7189 71.89%
Micronuclear - 0.5600 56.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation - 0.8237 82.37%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.6298 62.98%
Acute Oral Toxicity (c) III 0.7402 74.02%
Estrogen receptor binding + 0.6093 60.93%
Androgen receptor binding + 0.5559 55.59%
Thyroid receptor binding - 0.5238 52.38%
Glucocorticoid receptor binding - 0.5374 53.74%
Aromatase binding + 0.6561 65.61%
PPAR gamma - 0.5970 59.70%
Honey bee toxicity - 0.8886 88.86%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity - 0.6833 68.33%

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
CHEMBL221 P23219 Cyclooxygenase-1 97.84% 90.17%
CHEMBL2581 P07339 Cathepsin D 97.66% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.48% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.72% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 89.15% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.14% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.73% 91.11%
CHEMBL5028 O14672 ADAM10 86.26% 97.50%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.92% 95.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.52% 95.50%

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.
Salmea scandens

Cross-Links

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PubChem 86126116
LOTUS LTS0200243
wikiData Q104917580