Products

Catalog No	Chemical Name	CAS Number	Purity
L20351	PFM01	1558598-41-6	98% Min.
PFM01 is a nuclease-specific MRE11 inhibitor. PFM01 targets MRE11 at a site near the
L20349	Poloxin	321688-88-4	98% Min.
Poloxin is the first small-molecule inhibitor specifically targeting the function of
L20345	Prexasertib free base	1234015-52-1	98% Min.
Prexasertib, also know LY2606368, is a n inhibitor of checkpoint kinase 1 (chk1) with
L20333	Parsaclisib HCl	1995889-48-9	98% Min.
Parsaclisib, also known as INCB050465, is a novel PI3Kδ inhibitor which synergizes w
L20332	Parsaclisib free base	1426698-88-5	98% Min.
Parsaclisib, also known as INCB050465, is a novel PI3Kδ inhibitor which synergizes w
20294	Paltusotine ( CRN-00808 )	2172870-89-0	≧98.0%
Paltusotine is a new class of oral, selective, nonpeptide, somatostatin receptor type
20282	PS210	1221962-86-2	98% Min.
PS210 is a substrate-selective inhibitor of protein kinase PDK1. It acts by binding t
20278	PD-159206	171744-42-6	≧94.0%
PD-159206 is a nucleocapsid inhibitor. It exhibits good antiviral activity against HI
21227	3PO	18550-98-6	98% Min.
3PO is a PFKFB3 (6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase) inhibitor. 3PO
2073108	PF-06802861 ( ARRY 371797 ; ARRY-797 )	1034189-82-6	≧98.0%
ARRY 797 (also known as ARRY 371797 or PF 06802861) is an orally active, selective p3
2071623	PF-04745637	1917294-46-2	98% Min.
PF-04745637 is a TRPV1 antagonist.
2071607	Pepstatin	26305-03-3	98% Min.
Pepstatin inhibits the aspartic protease endothiapepsin.
2071540	PF-477736	952021-60-2	98% Min.
PF-477736, also known as PF-00477736, is a potent CHK1 inhibitor with potential chemo
2071506	PF-06869206	2227425-05-8	98% Min.
PF-06869206 is an Orally Bioavailable Selective Inhibitors of the Sodium-Phosphate Co
2071401	Pimodivir ( VX-787 )	1629869-44-8	98% Min.
Pimodivir, also known as VX-787, JNJ-872, is a novel inhibitor of influenza virus rep
2062201	p-Aminophenol sulfate	85278-22-4	98% Min.

2062020	3-PHENYL-1H-PYRAZOLE-4-CARBALDEHYDE	26033-20-5	96% Min.

2061707	Preladenant	377727-87-2	98% Min.
Preladenant, also known as SCH 420814, is a potent and selective antagonist at the ad
2061706	Paquinimod	248282-01-1	98% Min.
Paquinimod, also known as ABR‑215757, is a S100A9 inhibitor preventing S100A9 bindi
2061301	PDM-2	688348-25-6	98% Min.
PDM-2 is an analog of resveratrol acting as a potent and selective aryl hydrocarbon r
206701	PU-WS13	1454619-14-7	98% Min.
PU-WS13 is a potent, Grp94-specific Hsp90 inhibitor of the purine scaffold class. PU-
S-204148	2,6-Pyridinedicarboxaldehyde	5431-44-7	98% Min.

S-204141	Piperazine, 1-[(1aR,10bS)-1,1-difluoro-1,1a,6,10b-tetrahydrodibenzo[a,e]cyclopropa[c]cyclohepten-6-yl]-, hydrochloride (1:1), rel-	312905-21-8	96% Min.

193282	PZ-2891	2170608-82-7	>98%
PZ-2891 is a potent and selective, orally active Pantothenate kinase (PANK) modulator
193264	PF-06835919 ( MDK-1846 )	2102501-84-6	≧98.0%
MDK1846 is a potent ketohexokinase (KHK) inhibitor.
31619	PTI-428(PTI428)	1953130-87-4	98% Min.
PTI-428 is a type of CFTR modulator called an amplifier. Amplifiers increase the amou
1932011	PF-05085727	1415637-72-7	>98%
PF-05085727 is a Potent, Selective, and Brain Penetrant Phosphodiesterase 2A Inhibito
193206	Petesicatib	1252637-35-6	>98%
Petesicatib is a cathepsin inhibitor drug candidate.
193204	Pyridone 6	457081-03-7	>98%
Pyridone 6, also known CMP 6 or JAK Inhibitor I, is a pan-Janus-activated kinase inhi
193110	Pretomanid	187235-37-6	>98%
Pretomanid, aslo known as PA-824, a bioreductive drug. PA-824 has potent in vitro act