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WUN 33290, also known as Azido-PEG4-Amido-tri-(t-butoxycarbonylethoxymethyl)-methane is a branched PEG derivative...
WUN37241 is an analytical reference standard that is structurally similar to known opioids. WUN37241 is a byproduct...
WUN 37605, also known as N-(t-Boc-Aminooxy-PEG2)-N-bis(PEG3-propargyl) is a branched alkyne PEG Linker. PEG Linkers...
WUN 37718, also known as N-(Aminooxy-PEG2)-N-bis(PEG3-propargyl) is a branched alkyne PEG Linker. PEG Linkers may be...
WUN-387 is a functionalized cereblon ligand for PROTAC® research and development; incorporates an E3 ligase ligand...
WUN 39032, also known as PEG4-bis(phosphonic acid diethyl ester) is a PEG Linker. This product has no formal name at...
WUN40378 is compound first reported in PCT Int. Appl. (2019), WO 201909959, in which it was described as CBFβ-RUNX1...
WUN 53832, also known as N-(Azido-PEG2)-N-Boc-PEG4-t-butyl ester is a branched PEG derivative with a terminal azide...
WUN 59623, also known as 3-(2-bromoacetamido)propanoic acid NHS ester is a PEG derivative containing a bromide group...
CAS#: 2107273-82-3 (chloride)
WUN 73823, also known as N,N'-bis-(acid-PEG3)-Benzothiazole Cy5 is a PEG derivative containing a cyanine dye with...
WUN 78304, also known as Propargyl-PEG3-phosphonic acid ethyl ester is a PEG Linker. This product has no formal name...
WUN 81618, also known as Tri(t-butoxycarbonylethoxymethyl) ethanol is a branched PEG derivative with a terminal...
WWL113 is a selective, distinct Ces3 inhibitor.
WWL123 is a novel α/ß-hydrolase domain 6 (ABHD6) inhibitor.
WWL-154 is a serine hydrolase inhibitor. Serine hydrolases (SHs) are-one of the largest and most diverse enzyme...
WWL229 is a selective Ces3 inhibitor. It acts by inhibiting recombinant Ces3 but not Ces1f, ABHD6 or other tested...
WWL70 is a potent inhibitor of α/β-hydrolase domain 6 (ABHD6) (IC50 = 70 nM), an enzyme which catalyzes the...
WY-14643, also known as pirinixic acid, is a selective PPARα agonist. WY-14643 negatively inhibits NF-κB...
WYE-125132, also known as WYE-132, is a highly potent, ATP-competitive, and specific mTOR kinase inhibitor (IC(50):...
WYE-354 is a potent cell-permeable inhibitor of mTOR (IC50 = 4.3 nM) which blocks signaling through both mTOR complex...
WYE-687 is a potent and ATP-competitive and selective inhibitor of mTOR with IC50 of 7 nM.
WZ-3146 is a covalent or irreversible pyrimidine-based EGFR inhibitor against EGFR T790M. WZ-3146 was identified by...
WZ4002 is EGFR inhibitor against EGFR T790M (mutation of the gatekeeper T790 residue) which is detected in 50% of...
WZ4002-hydroxy is a WZ4002 (MedKoo Cat#: 203170) derivative or WZ4002 analog. In which the methoxy group is replaced...
WZ4003 is a selective inhibitors of the LKB1-tumour-suppressor-activated NUAK kinases. WZ4003 inhibits both NUAK...