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Catalog No CAS NO Product name
CR2470
1533426-72-0
SCR7
SCR7 is a specific DNA Ligase IV inhibitor. SCR7 inhibits end joining of double strand breaks in diverse cell types resulting in t..
CR2468
64232-83-3
L189
L189 is a DNA ligase I, III and IV inhibitor (IC50 values are 5, 9 and 5 μM respectively) that blocks DNA binding. L189 inhibits ..
CR2467
1454619-14-7
PU-WS13
PU-WS13 is a potent, Grp94-specific Hsp90 inhibitor of the purine scaffold class. PU-WS13 has been shown to reduce the viability o..
CR2464
1440209-96-0
BRD73954
BRD73954 is a small molecule inhibitor that potently inhibits HDAC6 and HDAC8. It inhibits HDAC6, a class IIb histone that deacety..
CR2462
174634-09-4
TAS-103 dihydrochloride
TAS-103, also known as BMS-247615, is a quinoline derivative that displays antitumor activity in murine and human tumor models. TA..
CR2461
174634-08-3
BMS-247615 TAS-103
TAS-103, also known as BMS-247615, is a quinoline derivative that displays antitumor activity in murine and human tumor models. TA..
CR2447
22978-25-2
GW9662
GW9662 is a potent, irreversible and selective PPARgamma antagonist, which prevented activation of PPARgamma and inhibited growth ..
CR2439
864082-47-3
GSK429286A
GSK429286A is a selective Rho-kinase inhibitor (IC50 values are 14, 780 and 1940 nM for ROCK1, RSK and p70S6K respectively). Rever..
CR2435
845714-00-3
PHA-767491 CAY10572
PHA-767491, also known as CAY10572, is a potent, ATP-competitive dual cdc7/cdk9 inhibitor (IC50 values are 10 and 34 nM respective..
CR2425
1174043-16-3
AZD2461
AZD2461 is a novel and potent PARP inhibitor with lower affinity to P-glycoprotein. AZD2641 is currently in Phase I clinical study..
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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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