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 About 10 results found for searched term "93-91-4" (0.055 seconds)

Cat.No.  Name Target
M1887 TG101209 JAK
TG101209 is a novel small molecule, ATP-competitive JAK2-selective kinase inhibitor (IC50 = 6 nM).
M3663 K-Ras(G12C) inhibitor 9 Ras
K-Ras(G12C) inhibitor 9 is an allosteric inhibitor of oncogenic K-Ras(G12C).
M13821 HJB97 Epigenetic Reader Domain
HJB97 is a high-affinity BET inhibitor with Kis of 0.9 nM (BRD2 BD1), 0.27 nM (BRD2 BD2), 0.18 nM (BRD3 BD1), 0.21 nM (BRD3 BD2), 0.5 nM (BRD4 BD1), 1.0 nM (BRD4 BD2), respectively.
M20597 PF-562271 HCl FAK
PF-562271 HCl is the hydrochloride salt of PF-562271, which is a potent, ATP-competitive, reversible inhibitor of FAK with IC50 of 1.5 nM, ~10-fold less potent for Pyk2 than FAK and >100-fold selectivity against other protein kinases, except for some CDKs. Phase 1.
M20695 TG-89 JAK
TG-89 is a JAK inhibitor that inhibits JAK2, FLT3, RET and JAK3.
M24857 Berlimatoxumab Others
ASN-2
Berlimatoxumab (ASN-2) is an antibody. Berlimatoxumab can be used for experiment research.
M24858 Bempegaldesleukin IL Receptor/Related
NKTR-214 BEMPEG
Bempegaldesleukin (NKTR-214), a PEGylated interleukin-2 (IL-2), is an immunostimulatory IL-2 prodrug acting as a CD122-preferential IL-2 pathway agonist. Bempegaldesleukin can stimulate an antitumor immune response.
M30830 Imirestat Aldose Reductase
AL 1576; Alcon 1576; HOE 843
Imirestat (AL 1576) is an aldose reductase inhibitor, used for the treatment of diabetes.
M44687 1-Phenylbutane-1,3-dione Others
1-Phenylbutane-1,3-dione is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
M49612 MMT3-72-M2 JAK
MMT3-72-M2 is an MMT3-72 metabolite.



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