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Signaling Pathways

Chemical Structure Cat. No. Product Name CAS No.
PXL51107 Chemical Structure
BCP28928 PXL51107 1627929-55-8
PLX51107 is a novel structurally distinct BET inhibitor that inhibits all four BET family proteins BRD2, BRD3, BRD4, and BRDT with low nanomolar potency.
Nidufexor Chemical Structure
BCP28929 Nidufexor 1773489-72-7
Nidufexor is a farnesoid X receptor (FXR) agonist.
Nampt-IN-1 Chemical Structure
BCP25239 Nampt-IN-1 1698878-14-6
Nampt-IN-1, also known as LSN3154567, is a potent and elective NAMPT inhibitor.
Pradefovir Chemical Structure
BCP28900 Pradefovir 625095-60-5
Pradefovir, also known as Remofovir, ICN-2001-3; MB-06866; MB-6866; ICN-20013, is a reverse transcriptase inhibitor potentially for treatment of chronic HBV infection.
MB 07133 Chemical Structure
BCP28904 MB 07133 685111-92-6
MB07133 is a novel cytarabine (araC) prodrug that uses the HepDirect technology to target production of the active form of araC, araC triphosphate (araCTP), to the liver.
 GTS-21 Chemical Structure
BCP28897 GTS-21 148372-04-7
2,4-Dimethoxybenzylidene Anabaseine selectively activates rat alpha7 receptors and improves memory-related behaviors in a mecamylamine-sensitive manner.
 LYN-1604 Chemical Structure
BCP28888 LYN-1604 2088939-99-3
LYN-1604 is a novel activator of ULK1, inducing cell death involved in ATF3, RAD21, and caspase3, accompanied by autophagy and apoptosis.
 LYN-1604 hydrochloride Chemical Structure
BCP28889 LYN-1604 hydrochloride LYN-1604HLC
LYN-1604 hydrochloride is a potent ULK1 agonist with an EC50 of 18.94 nM.
 LYC-55716 Chemical Structure
BCP28882 LYC-55716 2055536-64-4
LYC-55716 is novel oral RAR-related orphan receptor γ (RORγ) agonist.
 GSK872 Chemical Structure
BCP28887 GSK872 1346546-69-7
GSK872 (GSK2399872A) is a a receptor interacting protein kinase-3 (RIP3) inhibitor.
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