R11788 |
3-(3,4-Dihydroxyphenyl)acrylaldehyde |
N/A
|
R11789 |
A-83-01 |
A 83-01 is a potent inhibitor of TGF-β type I receptor ALK5 kinase, type I
|
R11790 |
Genz-644282 |
Genz-644282 is a non-camptothecin topoisomerase I inhibitor, used for
|
R11791 |
JNJ-40411813 (ADX-71149) |
JNJ-40411813 (ADX-71149) is a novel positive allosteric modulator of the me
|
R11792 |
Lomitapide mesylate (AEGR-733 mesylate; BMS-201038 mesylate) |
Lomitapide mesylate(AEGR-733; BMS-201038) is an inhibitor of microsomal triglyce
|
R11793 |
Lomitapide (AEGR-733; BMS-201038) |
Lomitapide (AEGR-733; BMS-201038) is a potent inhibitor of microsomal triglyceri
|
R11794 |
PF-562271 besylate (PF562271 besylate; PF 562271 besylate) |
PF-562271 besylate is a potent ATP-competitive, reversible inhibitor of FAK
|
R11795 |
TA103(BMS-247615) |
TAS-103 is a dual inhibitor of DNA topoisomerase I/II, used for cancer rese
|
R11796 |
MK-8998 |
MK-8998 (compound 33) is a potent and selective inhibitor of the T-type cal
|
R11797 |
LDC4297 |
LDC4297 is a potent and selective CDK7 inhibitor with an IC50&nbs
|
R11798 |
ETC-159 |
ETC-159 is a potent, orally available PORCN inhibitor. It inhibits β-c
|
R11799 |
P22077 |
P 22077 is a cell-permeable ubiquitin-specific protease 7 (USP7) inhibitor with
|
R11800 |
HC030031 |
HC-030031 is a potent and selective TRPA1 inhibitor, which antagonizes
|
R11801 |
P005091 |
P005091 is a selective and potent inhibitor of ubiquitin-specific protease
|
R11802 |
NSC74859 (S3I-201) |
NSC 74859 is a selective Stat3 inhibitor with an IC50 of 86 μM.
|
R11803 |
BAY876 |
BAY-876 is an oral and selective GLUT1 inhibitor with an IC50&nbs
|
R11804 |
4-bromo-6-methyl-1H-pyrrolo[2,3-c]pyridin-7(6H)-one |
N/A
|
R11805 |
4-bromo-6-methyl-1-tosyl-1H-pyrrolo[2,3-c]pyridin-7(6H)-one |
N/A
|
R11806 |
Bevantolol hydrochloride |
Bevantolol hydrochloride is a cardioselective, beta adrenoceptor antag
|
R11807 |
Firsocostat (ND-630; GS-0976; NDI-010976) |
Firsocostat (ND-630; GS-0976; NDI-010976) is an acetyl-CoA carboxylase (ACC) inh
|
R11808 |
Nepicastat (SYN117) |
Nepicastat (SYN117) is a selective, potent, and orally active inhibitor of
|
R11809 |
H-9 |
N/A
|
R11812 |
GSK872 |
GSK-872 is a RIPK3 inhibitor, which binds RIP3 kinase domain with an IC50 of 1.8
|
R11814 |
Pazopanib Hydrochloride (Synonyms: GW786034 (Hydrochloride)) |
Pazopanib Hydrochloride (GW786034 Hydrochloride) is a novel multi-target inhibit
|
R11815 |
7-ammonio-3-methyl-8-oxo-5-thia-1-azabicyclo[420]oct-3-ene-2-carboxylate |
N/A
|