(E,E,E)-N-(2-Methylpropyl)hexadeca-2,6,8-trien-10-ynamide

Details

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Internal ID c1eea0d8-2c4c-4022-8afe-14f30757242b
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty amides > N-acyl amines
IUPAC Name (2E,6E,8E)-N-(2-methylpropyl)hexadeca-2,6,8-trien-10-ynamide
SMILES (Canonical) CCCCCC#CC=CC=CCCC=CC(=O)NCC(C)C
SMILES (Isomeric) CCCCCC#C/C=C/C=C/CC/C=C/C(=O)NCC(C)C
InChI InChI=1S/C20H31NO/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-20(22)21-18-19(2)3/h10-13,16-17,19H,4-7,14-15,18H2,1-3H3,(H,21,22)/b11-10+,13-12+,17-16+
InChI Key OIPHBJBKSAKTTI-IVZWYUIFSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H31NO
Molecular Weight 301.50 g/mol
Exact Mass 301.240564612 g/mol
Topological Polar Surface Area (TPSA) 29.10 Ų
XlogP 6.00
Atomic LogP (AlogP) 4.79
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 10

Synonyms

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86926-57-0
(2E,6E,8E)-N-Isobutyl-2,6,8-hexadecatriene-10-yneamide
C08454
CHEBI:282
DTXSID001183053
(2E,6E,8E)-N-(2-methylpropyl)hexadeca-2,6,8-trien-10-ynamide
Q27105288
2,6,8-Hexadecatrien-10-ynamide, N-(2-methylpropyl)-, (E,E,E)-

2D Structure

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2D Structure of (E,E,E)-N-(2-Methylpropyl)hexadeca-2,6,8-trien-10-ynamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9845 98.45%
Caco-2 + 0.5746 57.46%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Lysosomes 0.4065 40.65%
OATP2B1 inhibitior - 0.8577 85.77%
OATP1B1 inhibitior + 0.8514 85.14%
OATP1B3 inhibitior + 0.9414 94.14%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.7353 73.53%
P-glycoprotein inhibitior - 0.5684 56.84%
P-glycoprotein substrate - 0.6123 61.23%
CYP3A4 substrate + 0.5383 53.83%
CYP2C9 substrate - 0.7974 79.74%
CYP2D6 substrate - 0.8864 88.64%
CYP3A4 inhibition - 0.9200 92.00%
CYP2C9 inhibition - 0.7191 71.91%
CYP2C19 inhibition - 0.8121 81.21%
CYP2D6 inhibition - 0.9173 91.73%
CYP1A2 inhibition + 0.5135 51.35%
CYP2C8 inhibition - 0.7594 75.94%
CYP inhibitory promiscuity - 0.5512 55.12%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6100 61.00%
Carcinogenicity (trinary) Non-required 0.5434 54.34%
Eye corrosion - 0.7258 72.58%
Eye irritation - 0.9455 94.55%
Skin irritation - 0.6563 65.63%
Skin corrosion - 0.8070 80.70%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6433 64.33%
Micronuclear - 0.8200 82.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation - 0.7325 73.25%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity - 0.6778 67.78%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity + 0.5535 55.35%
Acute Oral Toxicity (c) III 0.7464 74.64%
Estrogen receptor binding - 0.6034 60.34%
Androgen receptor binding + 0.5473 54.73%
Thyroid receptor binding + 0.7698 76.98%
Glucocorticoid receptor binding - 0.6891 68.91%
Aromatase binding + 0.5544 55.44%
PPAR gamma + 0.6543 65.43%
Honey bee toxicity - 0.9308 93.08%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.6863 68.63%
Fish aquatic toxicity + 0.8669 86.69%

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 97.60% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 95.72% 89.63%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 94.81% 97.29%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 94.32% 96.38%
CHEMBL221 P23219 Cyclooxygenase-1 93.33% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.55% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.42% 99.17%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 91.73% 92.86%
CHEMBL3359 P21462 Formyl peptide receptor 1 89.29% 93.56%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 88.40% 100.00%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 87.18% 89.34%
CHEMBL2885 P07451 Carbonic anhydrase III 87.03% 87.45%
CHEMBL3267 P48736 PI3-kinase p110-gamma subunit 86.37% 95.71%
CHEMBL256 P0DMS8 Adenosine A3 receptor 86.03% 95.93%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 86.02% 85.94%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.46% 94.45%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 85.29% 94.33%
CHEMBL3401 O75469 Pregnane X receptor 84.69% 94.73%
CHEMBL4227 P25090 Lipoxin A4 receptor 84.19% 100.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.48% 96.00%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 81.86% 96.47%
CHEMBL299 P17252 Protein kinase C alpha 81.61% 98.03%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.10% 91.11%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 81.07% 92.29%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.88% 90.71%
CHEMBL268 P43235 Cathepsin K 80.13% 96.85%

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 ageratifolia
Allium sativum
Gardenia jasminoides

Cross-Links

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PubChem 5281152
NPASS NPC181584
LOTUS LTS0035028
wikiData Q27105288