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Cat.No. Product name Product Description
R11916 Lanifibranor (IVA337) Lanifibranor is a pan peroxisome proliferator-activated receptor (PPAR
R11915 Nidufexor(LMB-763) Nidufexor is a farnesoid X receptor (FXR) agonist. 
R11917 Ningetinib Ningetinib is a potent, orally bioavailable small molecule tyrosine kinase inhib
R11918 Ningetinib Tosylate Ningetinib Tosylate is a potent, orally bioavailable small molecule tyrosine kin
R11919 Debio 0932 (Synonyms: CUDC-305) Debio 0932 is an orally active HSP90 inhibitor, with IC50s of 100
R11920 RGFP-966 RGFP966 is a highly selective HDAC3 inhibitor with an IC50 o
R11921 Trametinib DMSO solvate (GSK-1120212 (DMSO solvate);JTP-74057 (DMSO solvate)) Trametinib DMSO solvate (GSK-1120212 (DMSO solvate);JTP-74057 (DMSO solvate)) is
R11922 ZL004 ZL-004 could protect mice against 5-fluorouracil damage and raise peripheral blo
R11923 JNK-IN8 JNK-IN-8 is a potent JNK inhibitor with IC50s of 4.7 nM, 18.7 nM,
R11924 Namodenoson (Synonyms: CF-102; 2-Cl-IB-MECA) Namodenoson (CF-102) is a selective A3 adenosine receptor agonist (Ki = 0.33 nM)
R11925 Umeclidinium bromide (Synonyms: GSK573719A) Umeclidinium bromide is a novel mAChR antagonist. The affinity (Ki) of Umeclidin
R11926 CPI-169 CPI-169 racemate is the racemate of CPI-169. CPI-169 is a novel and potent EZH2
R11927 ML216 (Synonyms: CID-49852229) ML216(CID-49852229) is a potent inhibitor of the DNA unwinding activity of BLM h
R11929 TD139 TD139 is a novel high-affinity inhibitor of the galectin-3 carbohydrate binding
R11930 ARS853 ARS-853 is a selective, covalent KRASG12C inhibitor with an IC50&
R11931 EC330 EC330 is a leukemia inhibitory factor (LIF) inhibitor. 
R11932 (2R,3S)-Rel-2,3-bis(4-chlorophenyl)-2,3-butanediaMine N/A
R11933 5-bromo-4-chloro-6-iodothieno[2,3-d]pyrimidine CAS NO.:1799610-89-1 Product Name:Thieno[2,3-d]pyrimidine, 5-bromo-4-chloro-6-io
R11934 2-chloro-3-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol CAS NO.:1799612-10-4 Product Name:Phenol, 2-chloro-3-methyl-4-(4,4,5,5-tetrameth
R11935 SR17018 SR17018 is an mu-opioid-receptor (MOR) agonist, binding with GTPγS, with an EC50
R11936 SR-4370 SR-4370 is an inhibitor of HDAC, with IC50s of 0.13 μM, 0.58 μM, 0.006 μM, 2.3 μ
R11937 1-(Diphenylmethyl)-3-Azetidinone Hydrochloride (1:1) N/A
R11938 N-METHYLSALICYLAMIDE N/A
R11939 2-amino-4,5,6,7-tetrahydrobenzothiophene-3-carboxamide N/A
R11940 (1S,2R,3S,5R)-2-(Benzyloxymethyl)-6-oxabicyclo[3.1.0]hexan-3-ol N/A
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