16
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T71175 | SCD1 Inhibitor | ||
SCD1 Inhibitor is a novel stearoyl-CoA desaturase1 (SCD1) inhibitor. | |||
T38683 | SCD1 inhibitor-3 | SCD1-IN-3,SCD1 inhibitor-3,SCD1 inhibitor 17a | Dehydrogenase |
SCD1 inhibitor-3 (ML-270) is a highly effective and orally available compound that inhibits SCD1 with remarkable safety. SCD1 inhibitor-3 demonstrates strong potential for research in metabolic diseases, including obesit... | |||
T10525 | SCD1 inhibitor-4 | Dehydrogenase , Stearoyl-CoA Desaturase (SCD) | |
SCD1 inhibitor-4 is stearoylCoA desaturase-1 (SCD1) inhibitor. SCD1 inhibitor-4 can be used for the research of diabetes. | |||
T12863 | SCD1 inhibitor-1 | Others | |
SCD1 inhibitor-1 is a potent and liver-selective inhibitor of stearoyl-CoA desaturase-1 (SCD1). | |||
T2650 | MK-8245 | Dehydrogenase , Stearoyl-CoA Desaturase (SCD) | |
MK-8245 is a liver-targeting SCD inhibitor for human SCD1 (IC50: 1 nM) and for rat/mouse SCD1 (IC50: 3 nM), with anti-diabetic and anti-dyslipidemic function. | |||
T9003 | CVT-11127 | Dehydrogenase | |
CVT-11127 is an StearoylCoA Desaturase-1 (SCD1) inhibitor. | |||
T4515 | A939572 | Dehydrogenase , Stearoyl-CoA Desaturase (SCD) | |
A939572 is stearoyl-CoA desaturase1 (SCD1) inhibitor with IC50 values of <4 nM for mSCD1 and 37 nM for hSCD1. | |||
T16068 | MF-438 | Dehydrogenase , Stearoyl-CoA Desaturase (SCD) | |
MF-438 is an effective and orally bioavailable stearoyl-CoA desaturase 1 (SCD1) inhibitor (EC50: 2.3 nM for rSCD1). | |||
T1869 | PluriSIn 1 | NSC 14613,PluriSIn #1,PluriSln 1 | Apoptosis , Dehydrogenase , Stearoyl-CoA Desaturase (SCD) |
PluriSIn 1 (NSC 14613) is an inhibitor of stearoyl-CoA desaturase (SCD1), the key enzyme in oleic acid biosynthesis, revealing a unique role for lipid metabolism in hPSCs. | |||
T13356 | XEN723 | Dehydrogenase , Stearoyl-CoA Desaturase (SCD) | |
XEN723 is a potent thiazolylimidazolidinone Stearoyl-CoA Desaturase (SCD1) inhibitor(IC50s of 45 and 524 nM in mouse and HepG2 cell, respectively). | |||
T9722 | YTX-465 | Stearoyl-CoA Desaturase (SCD) | |
YTX-465 is an inhibitor of both stearoyl-CoA desaturase(IC50s = 39 nM) and Ole1 (IC50s = 30.4 μM). | |||
T14878 | CAY10566 | Dehydrogenase , Stearoyl-CoA Desaturase (SCD) | |
CAY10566 shows excellent cellular activity in blocking the conversion of saturated long-chain fatty acid-CoAs (LCFA-CoAs) to monounsaturated LCFA-CoAs in HepG2 cells (IC50=7.9 nM or 6.8 nM). CAY10566 is a potent, orally ... | |||
T61841 | SCD1-IN-1 | ||
SCD1-IN-1, a potent inhibitor of SCD1 (IC50: 5.8 nM), is valuable in dermatologic research [1]. | |||
T79262 | SSI-4 | Stearoyl-CoA Desaturase (SCD) | |
SSI-4 is a Stearoyl CoA desaturase 1 (SCD1) inhibitor that can be labeled with carbon-11 (11C) for use as a ligand in small animal in vivo PET/CT imaging studies of SCD1 [1]. | |||
T41253 | Sterculic acid | ||
Sterculic acid, a stearoyl-CoA desaturase-1 (SCD1) inhibitor, effectively suppresses delta-9 desaturase (Δ9D) activity in a dose-dependent manner, exhibiting an inhibition concentration (IC50) value of 0.9 μM [1]. | |||
T38844 | MK-8245 Trifluoroacetate | ||
MK-8245 trifluoroacetate is a phenoxy piperidine isoxazole derivative functioning as a potent, liver-targeting stearoyl-CoA desaturase (SCD) inhibitor, demonstrating significant anti-diabetic and anti-dyslipidemic effect... |