2,2-Dimethyl-N-(2,4,6-trimethoxyphenyl)dodecanamide

2,2-dimethyl-N-(2,4,6-trimethoxyphenyl)dodecanamide

Formula: C23H39NO4 (393.2879)
Chinese Name: 2,2-二甲基-N-(2,4,6-三甲氧基苯基)月桂酰胺
BioDeep ID: BioDeep_00000177472 ( View LC/MS Profile)
SMILES: CCCCCCCCCCC(C)(C)C(=O)NC1=C(OC)C=C(OC)C=C1OC



Found 2 Sample Hits

m/z Adducts Species Organ Scanning Sample
394.3017 [M+H]+
PPM:16.6
Rattus norvegicus Epididymis MALDI (DHB)
epik_dhb_head_ito08_47 - MTBLS58
Resolution: 17μm, 301x111

Description

394.3004 [M+H]+
PPM:13.3
Mus musculus Lung MALDI (DHB)
image5 - MTBLS2075
Resolution: 40μm, 163x183

Description

Supplementary Figure S8. MALDI-MSI data of mouse lung tissue administered with D9-choline and U 13C-DPPC–containing Poractant alfa surfactant (labels administered 18 h prior to sacrifice). Ion images of (a) m/z 796.6856 ([U13C-DPPC+Na]+), (b) m/z 756.5154 [PC32:0+Na]+ and (c) m/z 765.6079 ([D9-PC32:0+Na]+). (d) Overlay image of [U13C-DPPC+Na]+ (red) and [D9-PC32:0+Na]+ (green). Parts per million (ppm) mass errors are indicated in parentheses. All images were visualised using totalion-current normalisation and using hotspot removal (high quantile = 99%). DPPC = PC16:0/16:0.


D004791 - Enzyme Inhibitors PD 128042 (CI 976) is a potent, orally active, and selective inhibitor of ACAT (acyl coenzyme A:cholesterol acyltransferase) with an IC50s of 73 nM. PD 128042 is also a potent LPAT (lysophospholipid acyltransferase) inhibitor. PD 128042 inhibits Golgi-associated LPAT activity (IC50=15 μM). PD 128042 inhibits multiple membrane trafficking steps, including ones found in the endocytic and secretory pathway[1][2][3].