| R2304354 | 
            AS2863619 | 
            AS2863619 enables conversion of antigen-specific effector/memory T cells into Fo
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            | R2304355 | 
            BLU-945 | 
            BLU-945 is a potent, highly selective, reversible and orally active epidermal gr
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            | R2304356 | 
            VH032-cyclopropane-F | 
            VH032-cyclopropane-F is the VH032-based VHL ligand. VH032-cyclopropane-F can be 
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            | R2304357 | 
            TP-064 | 
            TP-064 is a potent and selective proteinarginine methyltransferase 4 (PRMT4; CAR
             | 
            
            
            
            
            | R2304358 | 
            MK-212 (CPP) hydrochloride | 
            MK-212 (CPP) monohydrochloride is a centrally acting 5-HT1C/5-HT2 agonist. MK-21
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            | R2304359 | 
            PF07104091 | 
            PF-07104091 inhibits CDK2, which may lead to cell cycle arrest, induce cell apop
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            | R2304360 | 
            INCB054329 | 
            INCB054329 is a potent BET inhibitor.
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            | R2304361 | 
            ML337 | 
            ML337 is a selective and brain-penetrant negative allosteric modulator of mGlu3,
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            | R2304362 | 
            BRAF inhibitor | 
            BRAF inhibitor is a B-Raf inhibitor extracted from patent WO/2011103196 A1, Comp
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            | R2304363 | 
            TD-106 | 
            TD-106 is a cereblon (CRBN) modulator, which can be used for targeted protein de
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            | R2304364 | 
            Argatroban | 
            Argatroban (MD-805) is a direct, selective thrombin inhibitor.
             | 
            
            
            
            
            | R2304365 | 
            Nilvadipine | 
            Nilvadipine is a potent calcium channel antagonist, and the IC50 value is around
             | 
            
            
            
            
            | R2304366 | 
            AZD7687 | 
            AZD7687 is a potent, selective, reversible and orally active diacylglycerol acyl
             | 
            
            
            
            
            | R2304367 | 
            L-6-Diazo-5-oxonorleucine; DON | 
            6-Diazo-5-oxo-L-nor-Leucine (L-6-Diazo-5-oxonorleucine; DON) is a glutamine anta
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            | R2304368 | 
            Azaserine | 
            Azazerine (CI-337) is a competitive inhibitor of glutamine amidotransferase. Aza
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            | R2304369 | 
            ML418 | 
            ML418 is a potent, selective and CNS penetrating Kir7.1 potassium channel blocke
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            | R2304370 | 
            ML289;VU0463597 | 
            ML289 (VU0463597) is a potent, selective, and CNS-penetrant mGlu3 (IC50=0.66 μM)
             | 
            
            
            
            
            | R2304371 | 
            MNI137 | 
            MNI137 is a potent and selective negative allosteric modulator for group II mGlu
             | 
            
            
            
            
            | R2304372 | 
            H3B-120 | 
            H3B-120 is a highly selective, competitive and allosteric carbamoyl phosphate sy
             | 
            
            
            
            
            | R2304374 | 
            FEN1-IN-4 | 
            FEN1-IN-4 (Compound 2) is a human flap endonuclease-1 (hFEN1) inhibitor.
             | 
            
            
            
            
            | R2304375 | 
            Ipsapirone (TVXQ7821) | 
            Ipsapirone (TVX Q 7821) is an anxiolytic compound and a 5-HT1A receptor partial 
             | 
            
            
            
            
            | R2304376 | 
            MRS1220 | 
            MRS1220, a highly potent and selective human A3 adenosine receptor (hA3AR) antag
             | 
            
            
            
            
            | R2304377 | 
            H2L5186303 | 
            H2L5186303 is a potent and selective LPA2 receptor (lysophosphatidic acid 2 rece
             | 
            
            
            
            
            | R2304378 | 
            PF-543 | 
            PF-543 (Sphingosine Kinase 1 Inhibitor II) is a potent, selective, reversible an
             | 
            
            
            
            
            | R2304379 | 
            PF-543 hydrochloride | 
            PF-543 hydrochloride (Sphingosine Kinase 1 Inhibitor II hydrochloride) is a pote
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