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产品目录

编号化学名称Cas号纯度化学结构
92210INCB8761 (PF-4136309)857679-55-198% 
INCB8761(PF-4136309) is a potent, selective, and orally bioavailable CCR2 antagonist.
91816IN000767301454700-89-098% 
Coming soon!
907123-(3-Iodophenyl)propanoic acid68034-75-398% 
Coming soon!
907113-(4-Iodophenyl)propionic acid1643-29-498% 
Coming soon!
82604Ipragliflozin761423-87-498% 
Ipragliflozin (ASP1941) is a highly potent and selective SGLT2 inhibitor with IC50 of
81920Indole-3-Acetamide879-37-898% 
Coming soon!
810054-iodo-7H-pyrrolo[2,3-d]pyrimidine1100318-96-497% 
Coming soon!
803163-Iodo-4-(trifluoromethoxy)benzoic acid1110709-70-097% 
Coming soon!
803133-iodo-4-isopropylbenzoic acid99059-64-097% 
Coming soon!
72806IDO inhibitor 11204669-37-399.01% by HPLC at 254nm 
IDO is an enzyme that catalyzes the degradation of the essential amino acid L-tryptop
72602Imisopasem-manganese(M40403)218791-21-098% 
M40403 is a low molecular weight, synthetic manganese containing superoxide dismutase
60809ICI118551(HCl)72795-01-898% 
Highly selective 2 adrenoceptor antagonist (Ki values are 1.2, 120 and 257 nM at 2, 1
252801intermediate-1(Abemaciclib)1231930-37-296%
4-fluoro-1-isopropyl-2-methyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-benz
52805Ivacaftor873054-44-598% 
Ivacaftor (VX-770) is a potentiator of CFTR targeting G551D-CFTR and F508del-CFTR wit
52747Ispinesib336113-53-298% 
Ispinesib (SB-715992) is a potent, specific and reversible inhibitor of KSP (HsEg5) w
52609INCB280601029712-80-898% 
INCB28060 is a novel orally active inhibitor (IC50=0.13 nM) of c-MET kinase.
52561Icilin36945-98-998% 
Icilin(AG 3-5) is a synthetic super-agonist of TRPM8 ion channel.
52543Inauhzin309271-94-198% 
Inauhzin(INZ) is a novel small molecule that effectively reactivates p53 by inhibitin
52527IOX2931398-72-098% 
IOX2 is a selective inhibitor of the Hypoxia Inducible Factor (HIF) Prolyl-Hydroxylas
51804Ibutamoren Mesylate159752-10-098% 
Ibutamoren mesylate (MK-0677) is an orally active nonpeptide growth hormone (GH) secr
52203IOWH0321191252-49-998% 
IOWH032 is a syntheticCFTRinhibitor withIC50of 1.01 M in CHO-CFTR cell based assays.
51637IU1314245-33-598% 
IU1 is a reversible and specific inhibitor of proteasome-associating Usp14. It does n