(E)-N-(2-phenylethyl)dec-2-en-4,6,8-triynamide

Details

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Internal ID 9c4adf85-f306-475a-bc33-849a174134bf
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name (E)-N-(2-phenylethyl)dec-2-en-4,6,8-triynamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H15NO/c1-2-3-4-5-6-7-11-14-18(20)19-16-15-17-12-9-8-10-13-17/h8-14H,15-16H2,1H3,(H,19,20)/b14-11+
InChI Key CIPVBKJMKXKOFD-SDNWHVSQSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H15NO
Molecular Weight 261.30 g/mol
Exact Mass 261.115364102 g/mol
Topological Polar Surface Area (TPSA) 29.10 Ų
XlogP 3.50
Atomic LogP (AlogP) 1.93
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (E)-N-(2-phenylethyl)dec-2-en-4,6,8-triynamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9965 99.65%
Caco-2 + 0.5722 57.22%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Lysosomes 0.4338 43.38%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8860 88.60%
OATP1B3 inhibitior + 0.9524 95.24%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.6867 68.67%
P-glycoprotein inhibitior - 0.8818 88.18%
P-glycoprotein substrate + 0.5092 50.92%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.8106 81.06%
CYP2D6 substrate - 0.8524 85.24%
CYP3A4 inhibition - 0.8286 82.86%
CYP2C9 inhibition - 0.5537 55.37%
CYP2C19 inhibition + 0.6160 61.60%
CYP2D6 inhibition - 0.9663 96.63%
CYP1A2 inhibition + 0.7347 73.47%
CYP2C8 inhibition + 0.4679 46.79%
CYP inhibitory promiscuity - 0.5740 57.40%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Non-required 0.6500 65.00%
Eye corrosion - 0.8066 80.66%
Eye irritation - 0.9736 97.36%
Skin irritation - 0.6786 67.86%
Skin corrosion - 0.8877 88.77%
Ames mutagenesis - 0.5354 53.54%
Human Ether-a-go-go-Related Gene inhibition - 0.6237 62.37%
Micronuclear - 0.5600 56.00%
Hepatotoxicity + 0.6948 69.48%
skin sensitisation - 0.7974 79.74%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.6770 67.70%
Acute Oral Toxicity (c) III 0.7259 72.59%
Estrogen receptor binding + 0.6453 64.53%
Androgen receptor binding + 0.6589 65.89%
Thyroid receptor binding - 0.6046 60.46%
Glucocorticoid receptor binding - 0.5870 58.70%
Aromatase binding + 0.7331 73.31%
PPAR gamma - 0.5390 53.90%
Honey bee toxicity - 0.9144 91.44%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity - 0.7338 73.38%

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 98.12% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 97.27% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.39% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.74% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 88.81% 94.73%
CHEMBL5028 O14672 ADAM10 86.15% 97.50%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.13% 91.11%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 86.09% 95.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.99% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.30% 95.56%
CHEMBL3902 P09211 Glutathione S-transferase Pi 80.72% 93.81%
CHEMBL5701 Q9H2K8 Serine/threonine-protein kinase TAO3 80.55% 96.67%
CHEMBL4208 P20618 Proteasome component C5 80.06% 90.00%

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.
Achillea santolinoides subsp. wilhelmsii

Cross-Links

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PubChem 14015868
LOTUS LTS0182544
wikiData Q104960091