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Cat. No.	Product Name	Field of Application
DC7588	PNU120596 Featured	PNU-120596 is a positive allosteric modulator of α7 nAChR with EC50 of 216 nM.
DC7648	PNU159682 Featured	PNU-159682 is a major bioactive metabolite of Nemorubicin in human liver microsomes; > 3,000-fold cytotoxic than its parent compound(MMDX and doxorubicin).
DC10409	PNU-74654	PNU-74654 is an inhibitor of Wnt/β-catenin pathway with an IC50 of 129.8 μM in NCI-H295 cell.
DC10760	Pocapavir Featured	Pocapavir is an investigational enterovirus (EV) capsid inhibitor.
DC6504	Patchouli Alcohol Featured	Pogostemon (patchouli) leaves and their extracted oils are used in perfumes and in traditional medicine to relieve sunstroke, stop vomiting, and increase appetite.
DC11373	Polmacoxib	Polmacoxib is an inhibitor of cyclooxygenase 2 (COX-2) and the carbonic anhydrase subtypes I (CAI) and CAII.
DC26094	Poloppin II	Poloppin II is an orally active, Poloppin derivative inhibitor of protein-protein interaction via the PBD of the mitotic Polo-like kinase (PLK) with IC50 of 41 uM in FP assays, exhibits IC50 of 61 nM cellular assay for mitotic arrest.
DC26116	Poloppin Featured	Poloppin is a cell-active, small molecule inhibitor of protein-protein interaction via the Polo-box domain (PBD) of the mitotic Polo-like kinase (PLK) with IC50 of 26.9 uM (PLK1) in FP assays.
DC9594	Poloxin Featured	Poloxin is a non-ATP competitive Polo-like Kinase 1 (PLK1) inhibitor that targets the polo-box domain.
DCAPI1298	Polydatin(Piceid)	Polydatin(Piceid)
DC10214	Polymyxin B sulphate Featured	Polymyxin B is an antibiotic primarily used for resistant gram-negative infections.
DC22413	Pomaglumetad Methionil	Pomaglumetad Methionil (LY2140023 monohydrate) is the methionine amide prodrug of the mGluR2/3 agonist LY-404039 with the potential oral treatment of schizophrenia..
DC26122	Pomalidomide-C2-NH2 hydrochloride	Pomalidomide-C2-NH2 hydrochloride is a synthesized E3 ligase ligand-linker conjugate that incorporates the Pomalidomide based cereblon ligand and a linker used in PROTAC technology.
DC26126	Cereblon Ligand-Linker Conjugates 9(E3 Ligase Ligand-Linker Conjugates 2) Featured	Pomalidomide-PEG4-Ph-NH2 is a synthesized E3 ligase ligand-linker conjugate that incorporates the Pomalidomide based cereblon ligand and 4-unit PEG linker used in PROTAC technology.
DC9742	Ponesimod Featured	Ponesimod(ACT-128800) is an orally active, selective sphingosine-1-phosphate receptor 1 (S1P1) immunomodulator with EC50 of 5.7 nM.
DC10829	Porcupine-IN-1 Featured	Porcupine-IN-1 is potent porcupine inhibitor with an IC50 of 0.5±0.2 nM.
DCAPI1093	Posaconazole Featured	Posaconazole (Noxafil) is a sterol C14ɑ demethylase inhibitor with an IC50 of 0.25 nM.
DC11914	Poseltinib Featured	Poseltinib (HM-71224, LY-3337641) is a potent and selective, covalent inhibitor of Btk with IC50 of 1.95 nM.
DCAPI1336	Potassium iodide	Potassium iodide
DC20217	Potassium thioacetate	Potassium thioacetate is widely used as a sulfur source in the synthesis of sulfur-containing organic compounds. It has been employed for the synthesis of heterocycles, polymers, transition-metal ligands, nanoparticles, bioactive compounds and macromolecu
DC7492	SB 258585 hydrochloride	Potent and selective 5-HT6 receptor antagonist (pKi = 8.6).
DC9213	GBR12783	Potent and selective DA uptake inhibitor
DC8022	R-268712 Featured	Potent and selective inhibitor of the TGF-β type I receptor/ALK5 (IC50 = 2.5 nM). Exhibits ~ 5000-fold selectivity over p38 MAPK. Suppresses development of renal fibrosis in a unilateral ureteral obstruction model. Also reduces proteinuria, glomeruloscler
DC8603	SR 49059 Featured	Potent and selective non-peptide vasopressin V1A receptor antagonist; devoid of agonist activity. Displays high affinity and efficacy at both rat (KI=1.6 nM) and human (KI -1.1 - 6.3 nM) V1A receptors.
DC8590	CRT-0066101 hydrochloride Featured	Potent inhibitor of protein kinase D (PKD); inhibits all PKD isoforms (IC50 values are 1, 2 and 2.5 nM for PKD1, PKD3 and PKD2 respectively).
DC7574	FIPI Featured	Potent phosholipase D (PLD) inhibitor (IC50 values are 20 and 25 nM for PLD2 and PLD1 respectively).
DC8604	Pim-1 Inhibitor 2	PIM1-IN-2 is a highly effective and ATP-competitive inhibitor of Pim-1, demonstrating a Ki value of 91 nM. Unlike traditional inhibitors, it interacts with the ATP-binding kinase hinge region without relying on the formation of standard hydrogen bonds, showcasing a unique mechanism of action. This distinctive approach highlights its potential as a promising therapeutic agent.
DC23003	hypocrellin A Featured	Potent PKC inhibitor. Photosensitizing agent. Potent antileishmanial agent.
DC7370	AZ-628 Featured	Potent, ATP-competitive inhibitor of Raf kinases (IC50 values are 29, 34 and 105 nM For c-Raf1, B-RafV600E and wild-type B-Raf, respectively). Displays selectivity For Raf kinases over a panel of 150 other kinases.
DC8484	KN-93(free base) Featured	Potent, cell permeable inhibitor of CaM kinase II (IC50 = 0.37 μM).

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