compound 23 — TargetMol Chemicals

Cat No.	Product Name	Synonyms	Targets
T8745	PROTAC BRAF-V600E degrader-1	Compound 23	Raf
	PROTAC BRAF-V600E degrader-1 (Compound 23) selectively induces degradation of BRAF-V600E but not wildtype BRAF.		Raf
Fr12799	AChE-IN-23
	AChE-IN-23 (compound 3h) is an inhibitor of acetylcholinesterase (AChE) with an IC 50 value of 48.3 μM [1].
T3222	16,17-Epoxypregnenol	16alpha,17alpha-Epoxypregnenolone	Others
	16,17-Epoxypregnenol is a useful organic compound for research related to life sciences. The catalog number is T3222 and the CAS number is 974-23-2.		Others
T63132	Amgen-23
	Amgen-23 (compound 23) is a potent inhibitor of sphingosine kinase (SPHK), acting on SPHK1 (IC50: 20 μM) and SPHK2 (IC50: 1.6 μM). amgen-23 can be used in anticancer studies.
T38192	Unifiram		Others
	Unifiram is a nootropic agent.1It increases acetylcholine (ACh) release in the rat cerebral cortexin vivoand induces a long-lasting increase in the amplitude of field excitatory postsynaptic potentials (fEPSPs) in the ra...		Others
T74999	Antibacterial agent 127
	Antibacterial agent 127 (Compound 23) is a potent antibacterial agent [1] .
T83556	(3β)-3-Hydroxyoleanan-12-one
	"(3β)-3-Hydroxyoleanan-12-one (compound 23), a natural product, is isolated from Codonopsis ovata [1]."
T63142	AChE/HDAC-IN-1
	COX-2-IN-23 (compound A10) is a potent inhibitor of AChE (IC50: 0.12 nM) and HDAC (IC50: 0.23 nM).COX-2-IN-23 exhibits antioxidant and metal chelating properties.COX-2-IN-23 can be used to study Alzheimer's disease.
T79769	HDAC6-IN-23		HDAC
	HDAC6-IN-23 (compound 9), an orally active inhibitor of HDAC6 [1], displays selective enzymatic inhibition.		HDAC
T62704	HBV-IN-23
	HBV-IN-23 (Compound 5k) is an inhibitor of HBV DNA replication (IC50: 0.58 μM). HBV-IN-23 inhibits drug-sensitive and drug-resistant strains. HBV-IN-23 induces apoptosis in HepG2 cells and exhibits anti-hepatocellular ca...
T61710	Antileishmanial agent-7
	Antileishmanial agent-7 (compound 23) exhibits strong antileishmanial activity against Leishmania donovani and L-6, with IC50 values of 6.89 and 259 μM, respectively [1].
T60841	SARS-CoV-2-IN-23
	SARS-CoV-2-IN-23 (compound GRL-0617) is an inhibitor of SARS-COV-2 papain-like protease (PLpro) (IC 50 = 2.3 μM) [1].
T63184	CDK5-IN-2
	CDK5-IN-2 (compound 15) is a highly selective CDK5 inhibitor that acts on CDK5/p25 (IC50: 0.2 nM) and CDK2/CycA (IC50: 23 nM).
T72097	Eleven-Nineteen-Leukemia Protein IN-2		Epigenetic Reader Domain
	Eleven-Nineteen-Leukemia Protein IN-2 (compound 23), an ENL inhibitor, exhibits an IC50 of 10.7 nM and is utilized for leukemia research [1].		Epigenetic Reader Domain
Fr16627	3,4-dihydro-2H-pyrido[3,2-b][1,4]oxazine
	Compound Fr16627 is a useful organic compound for research related to life sciences. The catalog number is Fr16627 and the CAS number is 20348-23-6.
T79166	KRAS G12C inhibitor 60		Ras
	KRAS G12C Inhibitor 60 (compound 23), a selective inhibitor targeting the Kras-G12C mutation, is utilized in the investigation of lung, colorectal, and pancreatic cancers [1].		Ras
T82098	ICMT-IN-44
	ICMT-IN-44 (compound 23) serves as an ICMT inhibitor with an IC50 value of 0.167 μM [1].
T74133	23-epi-26-Deoxyactein
	23-epi-26-Deoxyactein is a naturally occurring compound exhibiting anti-obesity and anti-cancer properties when administered orally [1] [2] [3].
T82082	IDO1-IN-23		Indoleamine 2,3-Dioxygenase (IDO)
	IDO1-IN-23 (compound 41) is a potent inhibitor of human indoleamine 2,3-dioxygenase 1 (IDO1), exhibiting an IC50 of 13 μM [1].		Indoleamine 2,3-Dioxygenase (IDO)
T77931	PROTAC IRAK3 degrade-1 formic		PROTACs
	PROTAC IRAK3 Degrade-1 (Compound 23) is a selective and potent IRAK3 degrader, demonstrating an IC50 value of 5 nM [1].		PROTACs