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Catalog No CAS NO Product name
CR3329
1373423-53-0
GSK-J4 HCl
GSK-J4 is a cell permeable, potent and selective histone demethylase. GSK-J4 is a prodrug of GSK J1, which is the first selective ..
CR3328
2158197-70-5
HS-1371
HS-1371 is a novel kinase inhibitor of RIP3-mediated necroptosis. HS-1371 directly binds to RIP3 in an ATP-competitive and time-in..
CR3327
1455091-10-7
FG-4592 intermediates
Synonyms: FG-4592 interMediate4-Hydroxy-7-phenoxy-3-isoquinolinecarboxylic acid methyl estermethyl 4-hydroxy-7-phenoxyisoquinoline..
CR3326
1421312-34-6
fg-4592 int 2
Synonyms:fg-4592 int 2methyl 4-hydroxy-1-methyl-7-phenoxyisoquinoline-3-carboxylate1 - methyl - 4 - hydroxy - 7 - phenoxy isoquino..
CR3325
2226517-76-4
SGC-GAK-1
SGC-GAK-1 is a potent, selective cyclin G-associated kinase (GAK) inhibitor with a Ki of 3.1 nM. SGC-GAK-1 is a chemical probe..
CR3324
911417-87-3
Belumosudil (KD025)
Belumosudil, also known as KD-025 and WHO11343, is an orally bioavailable inhibitor of ROCK-II that is greater than 200-fold selec..
CR3323
951395-08-7
Tafamidis meglumine
Tafamidis, also known as Fx-1006 or PF-06291826, is a drug for the amelioration of transthyretin-related hereditary amyloidosis (a..
CR3322
1361951-15-6
TP-3654
TP-3654 is a Pim-1 and Pim-3 kinase inhibitor potentially for the treatment of prostate cancer, acute myeloid leukemia, multiple s..
CR3321
942507-42-8
AZ304
AZ304 is a synthetic inhibitor designed to interact with the ATP-binding site of wild type and V600E mutant BRAF with IC50 val..
CR3320
198474-05-4
PF-06840003 EOS200271
PF-06840003, also known as EOS200271, is potent IDO-1 inhibitor (IC50 0.15 μM). PF-0684000 has moderate hIDO1 enzyme inhibition (..
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Products are chemical reagents for research use only and are not intended for human use. We do not sell to patients.
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