Home   >  
Protease/Metabolic Enzyme
  • Protease/Metabolic Enzyme

Classified by application

All Products

Signaling Pathways

Research Areas

Nature products






Raw Materials


Chemical Structure Cat. No. Product Name CAS No.
Rosiptor acetate Chemical Structure
BCP24919 Rosiptor acetate 782487-29-0
Rosiptor is a potent and selective SHIP1 activator. AQX-1125 inhibits Akt phosphorylation in SHIP1-proficient but not in SHIP1-deficient cells, reduces cytokine production in splenocytes, inhibits the activation of mast cells and inhibits human leukocyte chemotaxis. AQX-1125 suppresses leukocyte accumulation and inflammatory mediator release in rodent models of pulmonary inflammation and allergy.
Raphin1 acetate Chemical Structure
BCP48942 Raphin1 acetate 2242616-04-0
Raphin1 acetate is an orally bioavailable, selective inhibitor of the regulatory phosphatase PPP1R15B (R15B). Raphin1 acetate binds strongly to the R15B-PP1c holophosphatase with Kd of 0.033 μM.
Raphin1 Chemical Structure
BCP48938 Raphin1 2022961-17-5
Raphin1 is an orally bioavailable, selective inhibitor of the regulatory phosphatase PPP1R15B (R15B).
5-FAM tetrazine Chemical Structure
BCP48732 5-FAM tetrazine 1402432-77-2
NUN17724 Chemical Structure
BCP47020 NUN17724 765317-72-4
NUN17724 is a specific inhibitor of protein tyrosine phosphatase 1B (PTP1B).
Razuprotafib Chemical Structure
BCP46999 Razuprotafib 1008510-37-9
Razuprotafib, also known as AKB-9778, is a small-molecule inhibitor restoring Tie2 activation by inhibiting VE-PTP. In investigations against diabetes and COVID-19, razuprotafib is self-administered by patients through subcutaneous injection.
MP07-66 Chemical Structure
BCP46434 MP07-66 1938056-90-6
MP07-66, a FTY720 analogue, is devoid of immunosuppressive effects and shows promising antitumor effects in chronic lymphocytic leukemia by disruption of the SET-PP2A complex leading to PP2A reactivation.
ABBV-CLS-484 Chemical Structure
BCP45961 ABBV-CLS-484 2489404-97-7
ABBV-CLS-484 is a novel, orally bioavailable PTPN2 inhibitor for treatment of advanced or metastatic tumors.
SBI-425 Chemical Structure
BCP45955 SBI-425 1451272-71-1
SBI-425 is a potent, selective and orally bioavailable compound that robustly inhibits tissue-nonspecific alkaline phosphatase (TNAP) in vivo.
BVT948 Chemical Structure
BCP45529 BVT948 39674-97-0
BVT948 is a protein tyrosine phosphatase (PTP) inhibitor which can also inhibit several cytochrome P450 (P450) isoforms and lysine methyltransferase SETD8 (KMT5A).
123下一页末页共 61 条记录 1 / 7 页