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 About 8 results found for searched term "55-21-0" (0.138 seconds)

Cat.No.  Name Target
M4831 GSK2578215A LRRK2
GSK2578215A is a potent and selective LRRK2 kinase inhibitor with IC50 of 8.9 nM and 10.9 nM for LRRK2 (G2019S) and LRRK2 (WT), respectively.
M9139 Benzamide PARP
NSC 3114
Benzamide is an inhibitor of poly(ADP-ribose) polymerase with an IC50 of 3.3 μM.
M50387 NLS-StAx-h Wnt/beta-catenin
NLS-StAx-h is a selective, cell permeable, stapled peptide Wnt signaling inhibitor with an IC50 of 1.4 μM.
M50516 Isotocin Others
Isotocin ((Ser4,Ile8)-Oxytocin) is a polypeptide that can be found by peptide screening.
M3194 Nocodazole Src-bcr-Abl
Oncodazole;R17934
Nocodazole is a rapidly-reversible inhibitor of microtubule polymerization, also inhibits Abl, Abl(E255K) and Abl(T315I) with IC50 of 0.21 μM, 0.53 μM and 0.64 μM, respectively.
M5328 LDC000067 CDK
LDC067
LDC000067 is a highly selective CDK9 inhibitor with IC50 of 44 nM, 55/125/210/ >227/ >227-fold selectivity over CDK2/1/4/6/7.
M8723 PBOX-15 Others
PBOX-15 belongs to a group of tubulin-targeting pyrrolo-1,5-benzoxazepine (PBOX) compounds that potently induce apoptosis in a wide spectrum of cancer cells, including those originating from the four main types of leukemia and those exhibiting multi-drug resistance (IC50 = 155 nM/HL60-MDR1, 252 nM/HL60-ABCG2, 210 nM/HL60).
M31081 PF-07284892 Phosphatase
ARRY-558
PF-07284892 (ARRY-558) is a potent and orally activity SHP2 inhibitor with an IC50 value of 21 nM. PF-07284892 decreases theexpression of pERK.



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