Chemical
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- Catálogos PDF
Chemical Hay 28543 productos.
GNE-6776
GNE-6776 is a potent, selective USP7 inhibitor with oral activity.
Giredestrant
Giredestrant (GDC-9545, RG6171) is an orally active, selective estrogen receptor degrader (SERD) with best-in-class potential to compete with estradiol in the ER ligand binding domain and induce conformational changes.Giredestrant has antitumor activity.
GSK2879552 dihydrochloride
GSK2879552 dihydrochloride is an oral, irreversible LSD1/KDM1A inhibitor with antitumor activity.
SRS16-86
SRS16-86 is a potent inhibitor of ferroptosis. SRS16-86 is more metabolically and plasma-stable in vivo than Ferrostatin-1. SRS16-86 can be used for renal ischemia-reperfusion injury (IRI) and spinal cord injury (SCI) studies.
SRS16-86
SRS16-86 is a potent inhibitor of ferroptosis. SRS16-86 is more metabolically and plasma-stable in vivo than Ferrostatin-1. SRS16-86 can be used for renal ischemia-reperfusion injury (IRI) and spinal cord injury (SCI) studies.
Isobergapten
Isobergapten is a coumarin that regulates plant growth activity.
2,5-Dihydroxyacetophenone
2',5'-Dihydroxyacetophenone (DHAP, 2-Acetylhydroquinone, Quinacetophenone) is a mixture of dihydroxyacetophenone isomers used in food flavoring. 2',5'-Dihydroxyacetophenone significantly inhibits the production of NO by inhibiting the expression of iNOS. 2',5'-Dihydroxyacetophenone significantly reduces the expression levels of the pro-inflammatory...
Glycohyodeoxycholic acid
Glycohyodeoxycholic acid is the main metabolite of Hyodeoxycholic acid in human body, which can prevent the formation of gallstones.
Glycohyodeoxycholic acid
Glycohyodeoxycholic acid is the main metabolite of Hyodeoxycholic acid in human body, which can prevent the formation of gallstones.
Pyropheophorbide-a
Pyropheophorbide- A (Ppa) is a photosensitizer used in tumor photodynamic therapy (PDT).
Pyropheophorbide-a
Pyropheophorbide- A (Ppa) is a photosensitizer used in tumor photodynamic therapy (PDT).
Valbenazine
Valbenazine (NBI-98854) is a vesicular monoamine transporter-2 (VMAT2) inhibitor with a Ki of 110-190 nM.