JNJ DGAT2-A

Modify Date: 2024-01-20 11:40:12

JNJ DGAT2-A Structure
JNJ DGAT2-A structure
Common Name JNJ DGAT2-A
CAS Number 1962931-71-0 Molecular Weight 523.38
Density N/A Boiling Point N/A
Molecular Formula C24H16BrFN4O2S Melting Point N/A
MSDS N/A Flash Point N/A

 Use of JNJ DGAT2-A


JNJ-DGAT2-A is a selective diacylglycerol acyltransferase 2 (DGAT2) inhibitor with an IC50 value of 0.14 μM in human DGAT2-expressing Sf9 insect cell membranes. JNJ-DGAT2-A can be used for the research of triglyceride (TG) synthesis[1].

 Names

Name JNJ-DGAT2-A

 JNJ DGAT2-A Biological Activity

Description JNJ-DGAT2-A is a selective diacylglycerol acyltransferase 2 (DGAT2) inhibitor with an IC50 value of 0.14 μM in human DGAT2-expressing Sf9 insect cell membranes. JNJ-DGAT2-A can be used for the research of triglyceride (TG) synthesis[1].
Related Catalog
Target

IC50: 0.14 μM (Sf9 insect cell membranes DGAT2)[1]

In Vitro JNJ-DGAT2-A (5 μM) inhibits about 99% of recombinant DGAT2 enzymatic activity[1]. JNJ-DGAT2-A (5 μM) inhibits the DGAT activity in HepG2 cell lysates[1]. JNJ-DGAT2-A (0.3125, 0.625, 1.25, 2.5, 5, 10, and 20 µM; 60 min prior to isotope-labeled and additional 2 h after isotope-labeled) dose-dependently inhibits the generation of TG (52:2), TG (54:3), and TG (50:2) using 13C3-D5-glycerol as a substrate in HepG2 cells with IC50 values of 0.85 μM, 0.99 μM, and 0.66 μM, respectively[1].
References

[1]. Qi J, et al. The use of stable isotope-labeled glycerol and oleic acid to differentiate the hepatic functions of DGAT1 and -2. J Lipid Res. 2012 Jun;53(6):1106-16.

 Chemical & Physical Properties

Molecular Formula C24H16BrFN4O2S
Molecular Weight 523.38
Storage condition 2-8°C
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