About 6 results found for searched term "56-41-7" (0.174 seconds)
Cat.No. | Name | Target |
---|---|---|
M2476 | SEW2871 | S1P Receptor |
SEW-2871 | ||
SEW2871 is an orally active, potent, highly selective S1P1 (sphingosine-1-phosphate type 1 receptor) agonist, with an EC50 of 13.8 nM. SEW2871 activates ERK, Akt, and Rac signaling pathways and induces S1P1 internalization and recycling. | ||
M8477 | Indisulam | PROTAC |
E 7070 | ||
Indisulam is a carbonic anhydrase inibitor and antitumor CDK inhibitor. Indisulam targets the G1 phase of the cell cycle by depleting cyclin E. inducing p53 and p21, and inhibiting CDK2, causing a blockade in the G1/S transition. | ||
M9917 | Lipoteichoic acid | Adjuvants |
LTA | ||
Lipoteichoic acid (LTA) is a complex component of cell walls of Gram-positive bacteria that are involved in a wide range of cell processes such as the stimulation of immune responses and cell signaling pathways, also used as adjuvant. | ||
M10526 | L-Alanine | Metabolite/Endogenous Metabolite |
L-Alanine (also called 2-aminopropanoic acid, α-aminopropanoic acid) is an amino acid that helps the body convert the simple glucose into energy and eliminate excess toxins from the liver. | ||
M39405 | Fmoc-Phe(2-Cl)-OH | Amino Acid Derivatives |
Fmoc-Phe(2-Cl)-OH is a phenylalanine derivative. | ||
M45098 | CPS2 | PROTAC |
CPS2 is a first-in-class, highly potent, selective, and irreversible PROTAC CDK2 degrader (IC50= 24 nM) for AML-related studies. |
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