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Cat.No. Product Name / Activity Added
HY-100013 2-PCCA September 2017
HY-100013A (1R,2R)-2-PCCA September 2017
HY-100013B (1S,2S)-2-PCCA September 2017
HY-100014 KDM5A-IN-1 September 2017
KDM5A-IN-1 is an inhibitor histone demethylases.
HY-100015 Mivebresib September 2017
Mivebresib, a novel BET family inhibitor, disrupts critical transcription programs that drive prostate cancer growth to induce potent anti-tumor activity in vitro and in vivo.
HY-100016 AZD0156 September 2017
AZD0156 is an orally active, potent and selective <b>ATM kinase</b> inhibitor, used for cancer treatment.
HY-100017 BAY-876 September 2017
BAY-876 is the first highly selective GLUT1 inhibitor with IC50 of 0.
HY-100018 BAY1125976 September 2017
BAY1125976 is a selective allosteric <b> Akt1/2</b> inhibitor; inhibits Akt1 and Akt2 activity with <b>IC<sub>50</sub></b> values of 5.
HY-100019 BAY-1163877 September 2017
HY-10001A Calcipotriol (monohydrate) September 2017
Calcipotriol monohydrate is a synthetic VitD3 analogue with a high affinity for the <b>vitamin D</b> receptor.
HY-10002 Calcitriol September 2017
Calcitriol is the most active metabolite of vitamin D.
HY-100020 BAY-1436032 September 2017
HY-100021 CPI-1205 September 2017
CPI-1205, a highly potent and selective <b>EZH2</b> inhibitor (biochemical <b>IC<sub>50</sub></b>=2 nM, cellular <b>EC<sub>50</sub></b>=32 nM).
HY-100022 eFT508 September 2017
eFT508 is a potent, highly selective, and orally bioavailable <b>MNK1</b> and <b>MNK2</b> inhibitor, with <b>IC<sub>50</sub></b> of 1-2 nM against both of the two isoforms.
HY-100022A eFT-508 (hydrochloride) September 2017
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