| R2032958 |
AG-494 |
AG-494, a member of the tyrphostin family of tyrosine kinase inhibitors, is a po
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| R2032959 |
Anavex2-73 |
AVex-73 hydrochloride is a Sigma-1 Receptor agonist with an IC50 of 860 nM.
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| R2032960 |
HTL-1071 |
AZD4635 is a potent and selective, orally available adenosine A2A receptor (A2AR
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| R2032961 |
BPTU;BMS-646786 |
BPTU is a novel P2Y1 allosteric antagonist.
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| R2032962 |
CY-09 |
CY-09 is a selective and direct NLRP3 inhibitor.CY-09 directly binds to the ATP-
|
| R2032963 |
Danirixin |
Danirixin is a selective, and reversible CXCR2 antagonist, with IC50 of 12.5 nM
|
| R2032964 |
Esaxerenone |
Esaxerenone is a novel, highly potent and selective non-steroidal mineralocortic
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| R2032965 |
Fmoc-Val-ala-PAB |
Fmoc-Val-Ala-PAB, also known as Fmoc-Val-Ala-PAB-OH, is a useful linker for maki
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| R2032966 |
GSK-j5 |
GSK-J5 is a cell-permeable, inactive control for histone demethylase JMJD3/UTX i
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| R2032967 |
NCT-503 |
NCT-503 is a phosphoglycerate dehydrogenase (PHGDH) inhibitor with an IC50 of 2.
|
| R2032968 |
PF-06409577 |
PF-06409577 is a potent and selective allosteric activator of AMPK α1β1γ1 isofor
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| R2032969 |
TAK659 |
TAK-659 hydrochloride is a potent, selective and orally available spleen tyrosin
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| R2032970 |
TLR7-IN-1 |
TLR7 agonist 2 is a potent and selective Toll-like Receptor 7 (TLR7) agonist wit
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| R2032971 |
UCPH-101 |
UCPH-101 is an excitatory amino acid transporter subtype 1 (EAAT1) inhibitor wit
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| R2032972 |
ASK1-IN-1 |
GS-444217 is a potent, orally available and selective ATP-competitive inhibitor
|
| R2032973 |
LY2456302 |
Aticaprant (CERC-501) is a potent and centrally-penetrant kappa opioid receptor
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| R2032974 |
LY404187 |
LY-404187 is an ampakine, AMPA receptor potentiator.LY-404187 has been demonstra
|
| R2032975 |
mk8033 |
MK-8033 is a novel and specific dual ATP competitive c-Met/Ron inhibitor (IC50=1
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| R2032976 |
Ro28-2653 |
Ro 28-2653 is an inhibitor of matrix-metalloproteinases (MMPs) with high selecti
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| R2032977 |
Senexin B |
Senexin B is a potent, highly water-soluble and bioavailable CDK8/19 inhibitor,
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| R2032978 |
VU6005649 |
VU6005649 is a CNS penetrant mGlu7/8 receptor agonist with EC50s of 0.65 μM and
|
| R2032979 |
ABT702 dihydrochloride |
ABT-702 dihydrochloride is a potent adenosine kinase (AK) inhibitor (IC50=1.7 nM
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| R2032980 |
BAY1436032 |
BAY-1436032 is a novel pan-mutant isocitrate dehydrogenase 1 (IDH1) inhibitor.
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| R2032981 |
CH-223191 |
CH-223191 is a potent and specific antagonist of aryl hydrocarbon receptor (AhR)
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| R2032982 |
CPI-455 |
CPI-455 is a specific, pan-KDM5 inhibitor with an IC50 of 10 nM for KDM5A.CPI-45
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