About 8 results found for searched term "288-88-0" (0.302 seconds)
Cat.No. | Name | Target |
---|---|---|
M1758 | Foretinib | c-Met |
GSK089; EXEL-2880; XL880; GSK1363089 | ||
Foretinib (XL880, GSK1363089) is a multi-targeted inhibitor of c-Met and vascular endothelial growth factor receptor 2 (VEGFR2) with IC50 value of 0.4 nM for c-MET. | ||
M2318 | Ralimetinib dimesylate | p38 MAPK |
LY2228820 dimesylate; LY2228820 2MsOH | ||
Ralimetinib dimesylate (LY2228820 dimesylate) is a novel and potent inhibitor of p38 MAPK with IC50 of 7 nM. | ||
M39624 | 1,2,4-Triazole | Others |
1,2,4-Triazole is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||
M54822 | Rovazolac | Liver X Receptor |
ALX-101 | ||
Rovazolac is a liver x receptor (LXR) modulator, which can be used in the study of immune system disorders and atopic dermatitis. | ||
M1987 | LY2886721 | BACE |
LY2886721 is an effective, selective, orally active inhibitor of beta-site amyloid precursor protein lyase 1 (BACE1) with an IC50 of 20.3 nM against recombinant human BACE1. LY2886721 showed higher selectivity for BACE1 than cathepsin D, pepsin and renin, but lacked selectivity for BACE2 (IC50 was 10.2 nM). LY2886721 crosses the blood-brain barrier and can be used to study Alzheimer's disease. | ||
M11331 | UC2288 | Mdm2 |
UC2288 is a novel p21 attenuator with cellular permeability and oral activity (relatively selective activity for P21), based on the structural synthesis of sorafenib. UC2288 down-regulated the expression of P21 mRNA and reduced the level of P21 protein independently of p53, and had little effect on the stability of P21 protein. UC2288 did not inhibit VEGFR2 and Raf kinases, even at 10 μM. | ||
M21677 | Recombinant Human Follistatin 288 (HEK293, C-6His) | Cytokines and Growth Factors |
FST; follistatin isoform FST317 | ||
Follistatin 288 is a secreted glycoprotein that was first identified as a follicle-stimulating hormone inhibiting substance in ovarian follicular fluid . Human follistatin 288 cDNA encodes a 317 amino acid (aa) protein with a 29 aa signal sequence, and a 288 aa mature region. Recombinant Human Follistatin/FST is produced by Mammalian expression system and the target gene encoding Gly30-Asn317 is expressed with a 6His tag at the C-terminus. | ||
M30721 | Ralimetinib | p38 MAPK |
LY2228820 | ||
Ralimetinib (LY2228820) is a potent and selective, ATP-competitive inhibitor of p38 MAPK α/β, with IC50s of 5.3 and 3.2 nM, respectively. Ralimetinib (LY2228820) selectively inhibits phosphorylation of MK2 (Thr334), with no effect on phosphorylation of p38α MAPK, JNK, ERK1/2, c-Jun, ATF2, or c-Myc. |
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