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Catalog NoChemical NameCAS NumberPurityChemical Structure
51627MK76221227923-29-698% by HPLC 
MK-7622isused as adjunctive therapy to acetylcholinesterase inhibitors (AChEIs) for t
210507LP-261915412-67-8≧98.0%
LP-261 is a novel tubulin targeting anticancer agent that binds at the colchicine sit
20264ALC-03152036272-55-498% Min.
ALC-0315 is a synthetic cationic lipid (or ionizable lipid). It is a colorless oily m
20258CRT02737501979939-16-6≧98.0%
CRT0273750 modulates LPA levels in plasma and is suitable for in vivo studies.
16123054MK-10641207253-08-4≧98.0%
MK-1064 is a potent, selective and orally active Orexin OX2 Receptor Antagonist for p
51614AMG-9251401033-86-098% 
AMG925, Bulk in stock, contact us by email for detailed quotation.AMG-925 is a potent
21237Centanafadine ( free base )924012-43-198% Min.
Centanafadine (free base) is a dual norepinephrine-dopamine transporter inhibitor use
21236Centanafadine HCl923981-14-0≧98.0%
Centanafadine, also known as EB-1020, is an adrenergic uptake inhibitor and dopamine
20102901Razuprotafib1008510-37-9≧98.0%
Razuprotafib, also known as AKB-9778, is a small molecule inhibitor of vascular endot
2017878Elenbecestat ( E2609 )1388651-30-6≧98.0%
Elenbecestat (E2609) is a potent, orally bioavailable and CNS-penetrant BACE-1 inhibi
51607VE-822 ( Berzosertib )1232416-25-9≧98.0% 
VE-822(Berzosertib), an analogue of VE-821 with increased potency and selectivity aga
2073103Remibrutinib ( LOU064 )1787294-07-898% Min.
Remibrutinib ( LOU064 ) is a Potent and Highly Selective Covalent Inhibitor of Bruton