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 About 8 results found for searched term "92-78-4" (0.053 seconds)

Cat.No.  Name Target
M2011 PP121 VEGFR/PDGFR
PP121 is a dual inhibitor of tyrosine and phosphoinositide kinases.
M7405 TFC 007 Others
TFC 007 is a potent hematopoietic prostaglandin D synthase (H-PGDS) inhibitor.
M8424 KC7F2 HIF
KC7F2 is a cell permeable potent hypoxia inducible factor-1 (HIF-1) pathway inhibitor, with IC50 of 20 μM in LN229-HRE-AP cells, and with potential as a cancer therapy agent.
M14843 PQR620 mTOR
PQR620 is an orally bioavailable and selective brain penetrant inhibitor of mTORC1/2.
M27778 (3S,4S)-Tofacitinib JAK
(3S,4S)-Tofacitinib is the less active S-enantiomer of Tofacitinib. Tofacitinib inhibits JAK3 with IC50 of 1 nM.
M27779 PP30  mTOR
PP30, a TORKinib, is a potent, selective, and ATP-competitive inhibitor of mTOR with an IC50 of 80 nM.
M29030 PQR626  mTOR
PQR626, a rapamycin derivative, is a potent, selective, orally active, and brain-penetrant mTOR inhibitor, with an IC50 and Ki of 5 nM and 3.6 nM, respectively. PQR626 can be can be used for the research of neurological disorders.
M30926 Naphthol AS-E  Histone Acetyltransferase
Naphthol AS-E is a potent and cell-permeable inhibitor of KIX-KID interaction. Naphthol AS-E directly binds to the KIX domain of CBP (Kd:8.6 µM), blocks the interaction between the KIX domain and the KID domain of CREB with IC50 of 2.26 µM. Naphthol AS-E can be used for cancer research.



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