R2033182 |
KL-1333 |
NQO1 activator 1 is an orally available NAD+ modulator.It reacts with NAD(P)H:qu
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R2033183 |
BAY2335218 |
AHR antagonist 1 is an aryl hydrocarbon receptor (AHR) antagonist extracted from
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R2033184 |
ITI214 |
ITI-214 is a picomolar PDE1 inhibitor with excellent selectivity against other P
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R2033185 |
LXS196 |
LXS196 is a potent, selective and orally active protein kinase C (PKC) inhibitor
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R2033186 |
SY-1365 |
SY-1365 is a highly selective covalent inhibitor of CDK7.SY-1365 possesses thera
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R2033187 |
Vecabrutinib |
Vecabrutinib is a potent, noncovalent BTK and ITK inhibitor, with Kd of 0.3 nM a
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R2033188 |
PT2385;PT-2385 |
PT-2385 is a selective HIF-2α inhibitor with a Ki of less than 50 nM.
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R2033189 |
BTdCPU |
BTdCPU is a potent heme-regulated eIF2α kinase (HRI) activator.BTdCPU promotes e
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R2033190 |
CFTR corrector 2 |
CFTR corrector 2 is a cystic fibrosis transmembrane conductance corrector (CFTR)
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R2033191 |
LML-134;LML134 |
LML134 (compound 18b) is an orally active and high selective Histamine 3 recepto
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R2033192 |
PLX5622 |
PLX5622 is a highly selective brain penetrant and oral active CSF1R inhibitor wi
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R2033193 |
S29434 |
S29434 (NMDPEF) is a potent, competitive, selective and cell-permeable inhibitor
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R2033194 |
TAS0728 |
TAS0728 is a potent, selective, oral active, irreversible and covalent-binding H
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R2033195 |
AB928 |
AB928 is an orally bioavailable, selective dual adenosine receptor (A2aR/A2bR) a
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R2033196 |
SATA |
N-Succinimidyl S-acetylthioacetate (SATA), a protein modification agent, introdu
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R2033197 |
PA-6 |
IK1 inhibitor PA-6 (PA-6), a pentamidine analogue, is a selective and potent IK1
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R2033198 |
S119-8 |
S119-8 is a broad spectrum inhibitor of influenza A and B viruses.
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R2033199 |
LM22B-10 |
LM22B-10 is an activator of TrkB/TrkC neurotrophin receptor, and can induce TrkB
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R2033200 |
LY2444296 |
LY2444296 is an orally bioavailable, high-affinity and selective short-acting ka
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R2033201 |
CINPA1 |
CINPA1 is a potent and specific inhibitor of constitutive androstane receptor (C
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R2033202 |
GNF4877 |
GNF4877 is a potent DYRK1A and GSK3β inhibitor with IC50s of 6 nM and 16 nM, res
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R2033203 |
ML792 |
ML-792 is a specific small ubiquitin-like modifier (SUMO)-activating enzyme (SAE
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R2033204 |
AT007 |
AT-007 is an orally active central nervous system (CNS) penetrant Aldose Reducta
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R2033205 |
BAY293 |
BAY-293, a valuable chemical probe, blocks RAS activation via disruption of the
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R2033206 |
GS4361;IDO-IN-13 |
IDO-IN-13 is a potent indoleamine 2,3-dioxygenase 1 (IDO1) inhibitor with an EC5
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