Deca-2z-en-6,8-diynoic acid phenethylamide

Details

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Internal ID 5a187c85-891f-4c94-97b3-e5ffb8c829ed
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name (Z)-N-(2-phenylethyl)dec-2-en-6,8-diynamide
SMILES (Canonical) CC#CC#CCCC=CC(=O)NCCC1=CC=CC=C1
SMILES (Isomeric) CC#CC#CCC/C=C\C(=O)NCCC1=CC=CC=C1
InChI InChI=1S/C18H19NO/c1-2-3-4-5-6-7-11-14-18(20)19-16-15-17-12-9-8-10-13-17/h8-14H,6-7,15-16H2,1H3,(H,19,20)/b14-11-
InChI Key LKFULPKPZWWAEM-KAMYIIQDSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C18H19NO
Molecular Weight 265.30 g/mol
Exact Mass 265.146664230 g/mol
Topological Polar Surface Area (TPSA) 29.10 Ų
XlogP 3.70
Atomic LogP (AlogP) 2.71
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 Deca-2z-en-6,8-diynoic acid phenethylamide

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 + 0.6897 68.97%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Lysosomes 0.4357 43.57%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8743 87.43%
OATP1B3 inhibitior + 0.9523 95.23%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.4732 47.32%
P-glycoprotein inhibitior - 0.8253 82.53%
P-glycoprotein substrate - 0.5460 54.60%
CYP3A4 substrate + 0.5335 53.35%
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 + 0.6035 60.35%
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 - 0.9592 95.92%
Skin irritation - 0.6921 69.21%
Skin corrosion - 0.8870 88.70%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4368 43.68%
Micronuclear - 0.5600 56.00%
Hepatotoxicity + 0.5468 54.68%
skin sensitisation - 0.8237 82.37%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.6604 66.04%
Acute Oral Toxicity (c) III 0.7402 74.02%
Estrogen receptor binding - 0.4750 47.50%
Androgen receptor binding + 0.7294 72.94%
Thyroid receptor binding - 0.5280 52.80%
Glucocorticoid receptor binding - 0.6035 60.35%
Aromatase binding + 0.7771 77.71%
PPAR gamma - 0.5173 51.73%
Honey bee toxicity - 0.9260 92.60%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.5300 53.00%
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
CHEMBL2581 P07339 Cathepsin D 98.02% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 96.68% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.37% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.57% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.44% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 87.55% 94.73%
CHEMBL5028 O14672 ADAM10 87.41% 97.50%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.52% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.96% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.17% 96.00%

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.
Acmella oleracea
Salmea scandens

Cross-Links

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PubChem 129834550
LOTUS LTS0235991
wikiData Q105153042