| R2030157 |
MX-69 |
MX69 is an inhibitor of MDM2/XIAP, used for cancer treatment.
|
| R2030158 |
10074-G5 |
10074-G5 is an inhibitor of c-Myc-Max dimerization with an IC50 of 146 μM.
|
| R2030159 |
BIA 10-2474 |
BIA 10-2474 is an inhibitor of fatty acid amide hydrolase (FAAH) with IC50 value
|
| R2030160 |
S107 |
S107 is an orally available, blood brain barrier-permeable compound, which stabi
|
| R2030161 |
S49076 hydrochloride;S-49076 hydrochloride |
S49076 is a novel, potent inhibitor of MET, AXL/MER, and FGFR1/2/3 with IC50 val
|
| R2030162 |
Thiomyristoyl |
Thiomyristoyl is a potent and specific SIRT2 inhibitor with an IC50 of 28 nM.
|
| R2030163 |
UK-371804 |
UK-371804 is a urokinase-type plasminogen activator (uPA) inhibitor with a Ki of
|
| R2030164 |
LW6 (HIF-1α inhibitor; LW8) |
LW6 (HIF-1α inhibitor) is a novel HIF-1 inhibitor with an IC50 of 4.4 μM. LW6 de
|
| R2030165 |
FIN56 |
FIN56 is a specific inducer of ferroptosis.
|
| R2030167 |
Bay 41-4109 racemate |
BAY 41-4109 racemate is the racemate of BAY 41-4109. BAY 41-4109 is a potent inh
|
| R2030169 |
GJ103 |
GJ103 is an active analog of the read-through compound GJ072.
|
| R2030170 |
ISCK03 |
ISCK03 is a specific SCF/c-Kit inhibitor.
|
| R2030171 |
HSP70-IN-1 |
HSP70-IN-1 is a heat shock protein (HSP) inhibitor; inhibits the growth of Kasum
|
| R2030172 |
PD-166866;PD166866 |
PD166866 is a selective FGFR1 tyrosine kinase inhibitor with an IC50 of 52.4 nM.
|
| R2030173 |
GW506033X;PKR-IN-C16 |
PKR-IN-C16 is a specific protein kinase (PKR) inhibitor. PKR-IN-C16 is able to i
|
| R2030174 |
s49076 |
S49076 is a novel, potent inhibitor of MET, AXL/MER, and FGFR1/2/3 with IC50 val
|
| R2030176 |
Nodinitib-1 (ML130; CID-1088438) |
Nodinitib-1 (ML130;CID-1088438) is a NOD1 inhibitor with an IC50 of 0.56 μM.&nbs
|
| R2030178 |
Sugammadex |
Sugammadex sodium is a synthetic γ-cyclodextrin derivative, and acts as a new re
|
| R2030179 |
XL019 |
XL019 is a potent,orally active, and selective JAK2 inhibitor, with IC50s o
|
| R2030182 |
Amuvatinib (MP470; HPK 56) |
Amuvatinib (MP470) is an orally bioavailable multi-targeted tyrosine kinase inhi
|
| R2030183 |
PHT 427 |
PHT-247 is an inhibitor of the pleckstrin homology (PH) domain of Akt, and it is
|
| R2030184 |
NQDI-1 |
NQDI 1, an inhibitor of ASK1(apoptosis signal-regulating kinase 1), attenua
|
| R2030185 |
EMD534085 |
EMD534085 is a potent and selective inhibitor of the mitotic kinesin-5 with an I
|
| R2030186 |
Ly2584702 tosylate |
LY-2584702 tosylate salt is a selective ATP competitive inhibitor of p70S6K with
|
| R2030187 |
SHP099 hydrochloride |
SHP099 hydrochloride is a potent, selective and orally available SHP2 inhibitor
|