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 About 9 results found for searched term "66-84-2" (0.055 seconds)

Cat.No.  Name Target
M2807 LDN-57444 Deubiquitinase
LDN-57444 is a reversible, competitive proteasome inhibitor for Uch-L1 with IC50 of 0.88 μM, 28-fold selectivity over isoform Uch-L3.
M3280 Clopidogrel P2 Receptor
SR-25990C; Clopidogrelum
Clopidogrel is an oral, thienopyridine class antiplatelet agent used to inhibit blood clots in coronary artery disease, peripheral vascular disease, and cerebrovascular disease.
M6292 Ansamitocin P 3 Microtubule
Antibiotic C 15003P3; Maytansinol butyrate
Ansamitocin P-3 is a microtubule inhibitor, it is also a macrocyclic antitumor antibiotic.
M14086 Glucosamine hydrochloride Metabolite/Endogenous Metabolite
D-(+)-Glucosamine hydrochloride; Chitosamine hydrochloride
Glucosamine hydrochloride (D-Glucosamine hydrochloride) is an amino sugar and a prominent precursor in the biochemical synthesis of glycosylated proteins and lipids, is used as a dietary supplement.
M20730 KGA-2727 SGLT
KGA-2727 is a potent, selective, high-affinity inhibitor of sodium glucose cotransporter 1 (SGLT1) with Ki of 97.4 nM and 43.5 nM for human SGLT1 and rat SGLT1, respectively. The selectivity ratios (Ki for SGLT2/Ki for SGLT1) of KGA-2727 are 140 (human) and 390 (rat). KGA-2727 exhibits antidiabetic efficacy in rodent models.
M21293 BCPyr BTK
BCPyr is a new candidate BTK degradation agent (DC50 = 800 nM).
M30749 UCK2 Inhibitor-2  Dehydrogenase
UCK2 Inhibitor-2 is a non-competitive uridine-cytidine kinase 2 (UCK2) inhibitor with an IC50 value of 3.8 µM. UCK2 Inhibitor-2 can suppress uridine salvage in cells.
M51669 Cys-Arg-Gly-Asp-Phe-Pro-Ala-Ser-Ser-Cys (Disulfide bridge:cys1-cys10) Others
Cys-Arg-Gly-Asp-Phe-Pro-Ala-Ser-Ser-Cys (Disulfide bridge:cys1-cys10), a decapeptide containing a cyclic RGD active sequence, is an Integrin αIIbβ3 antagonist that inhibits platelet and Adhesion of proMMP-13.
M51940 Z-D-Lys(Boc)-OH Amino Acid Derivatives
Z-D-Lys(Boc)-OH is a lysine derivative.



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