(Z)-N-methoxy-16-pyridin-3-ylhexadec-7-yn-1-imine

Details

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Internal ID 154900c6-33e0-4851-8004-1c328473c533
Taxonomy Organoheterocyclic compounds > Pyridines and derivatives
IUPAC Name (Z)-N-methoxy-16-pyridin-3-ylhexadec-7-yn-1-imine
SMILES (Canonical) CON=CCCCCCC#CCCCCCCCCC1=CN=CC=C1
SMILES (Isomeric) CO/N=C\CCCCCC#CCCCCCCCCC1=CN=CC=C1
InChI InChI=1S/C22H34N2O/c1-25-24-20-15-13-11-9-7-5-3-2-4-6-8-10-12-14-17-22-18-16-19-23-21-22/h16,18-21H,2,4,6-15,17H2,1H3/b24-20-
InChI Key VKZMFWBBVBIKET-GFMRDNFCSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C22H34N2O
Molecular Weight 342.50 g/mol
Exact Mass 342.267113712 g/mol
Topological Polar Surface Area (TPSA) 34.50 Ų
XlogP 6.80
Atomic LogP (AlogP) 5.94
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 14

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (Z)-N-methoxy-16-pyridin-3-ylhexadec-7-yn-1-imine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9702 97.02%
Caco-2 + 0.5623 56.23%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.6380 63.80%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8883 88.83%
OATP1B3 inhibitior + 0.9454 94.54%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior + 0.8482 84.82%
P-glycoprotein inhibitior - 0.6240 62.40%
P-glycoprotein substrate - 0.7482 74.82%
CYP3A4 substrate + 0.5214 52.14%
CYP2C9 substrate - 0.8016 80.16%
CYP2D6 substrate - 0.7714 77.14%
CYP3A4 inhibition - 0.5804 58.04%
CYP2C9 inhibition - 0.6726 67.26%
CYP2C19 inhibition - 0.6019 60.19%
CYP2D6 inhibition - 0.8246 82.46%
CYP1A2 inhibition - 0.5206 52.06%
CYP2C8 inhibition + 0.8369 83.69%
CYP inhibitory promiscuity - 0.5815 58.15%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7409 74.09%
Carcinogenicity (trinary) Non-required 0.5436 54.36%
Eye corrosion - 0.9085 90.85%
Eye irritation - 0.7395 73.95%
Skin irritation - 0.6191 61.91%
Skin corrosion - 0.8380 83.80%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9322 93.22%
Micronuclear - 0.6700 67.00%
Hepatotoxicity - 0.7125 71.25%
skin sensitisation - 0.6776 67.76%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity - 0.6889 68.89%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.6948 69.48%
Acute Oral Toxicity (c) III 0.6545 65.45%
Estrogen receptor binding + 0.6691 66.91%
Androgen receptor binding - 0.7731 77.31%
Thyroid receptor binding + 0.6720 67.20%
Glucocorticoid receptor binding - 0.5778 57.78%
Aromatase binding - 0.5867 58.67%
PPAR gamma + 0.6480 64.80%
Honey bee toxicity - 0.8593 85.93%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.6600 66.00%
Fish aquatic toxicity - 0.7143 71.43%

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 96.96% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.25% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.99% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.99% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.17% 86.33%
CHEMBL3975 P09467 Fructose-1,6-bisphosphatase 87.96% 92.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.09% 99.17%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 85.05% 85.30%
CHEMBL2885 P07451 Carbonic anhydrase III 84.57% 87.45%
CHEMBL226 P30542 Adenosine A1 receptor 84.48% 95.93%
CHEMBL2535 P11166 Glucose transporter 84.24% 98.75%
CHEMBL1744525 P43490 Nicotinamide phosphoribosyltransferase 84.04% 96.25%
CHEMBL5203 P33316 dUTP pyrophosphatase 83.92% 99.18%
CHEMBL2996 Q05655 Protein kinase C delta 83.75% 97.79%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.82% 95.89%
CHEMBL5805 Q9NR97 Toll-like receptor 8 82.30% 96.25%
CHEMBL3401 O75469 Pregnane X receptor 81.76% 94.73%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.73% 100.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.57% 96.00%

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 101626230
LOTUS LTS0044724
wikiData Q105111501