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Catalog No CAS NO Product name
CR3243
1627607-87-7
PFI-2 HCl
PFI-2 is a potent inhibitor of SETD7 with IC50 2 nM and 1000-fold selectivity over other methyltransferases and other non-epigenet..
CR3242
71203-35-5
ML141
ML141 (CID-2950007) is demonstrated to be a potent, selective and reversible non-competitive inhibitor of Cdc42 GTPase suitable fo..
CR3240
1883711-97-4
AM-0902
AM-0902 is a potent and selective Transient Receptor Potential A1 (TRPA1) Antagonist Demonstrating Potent in Vivo Activity with ph..
CR3239
887686-02-4
OSS-128167
OSS_128167 is a selective SIRT6 inhibitor with IC50s of 89, 1578 and 751 μM for SIRT6, SIRT1 and SIRT2, respectively. OSS_128167 ..
CR3238
27314-97-2
Tirapazamine
Trapazamine, also known as SR-4233,DNA-damaging drug potentially for the treatment of cervical carcinoma, head and neck cancer. Ti..
CR3237
169274-78-6
Ro 25-6981
Ro 25-6981 is a highly potent and selective blocker of N-methyl-D-aspartate receptors containing the NR2B subunit. Ro 25-6981 inhi..
CR3236
459836-30-7
PEAQX NVP-AAM077
PEAQX, also known as NVP-AAM077; is a competitive antagonist at the NMDA receptor. Although originally described as 100-fold selec..
CR3235
1219737-12-8
MK-3903
MK-3903 is a potent and selective AMPK activator (EC50 = 8 nM). MK-3903 exhibited robust target engagement in mouse liver followin..
CR3234
1282041-94-4
DSM265
DSM265 is a long-duration, potent and selective dihydroorotate dehydrogenase (DHODH)) inhibitor. DSM265 is potential useful for th..
CR3233
895519-90-1
Flumatinib
Flumatinib, also known as HHGV678 , is a selective inhibitor of BCR-ABL/PDGFR/KIT. Flumatinib is currently in Phase I and II clini..
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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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