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| Cat.No. | Product name | Product Description |
| R910264 | DC661 | DC661 is a potent palmitoyl-protein thioesterase 1 (PPT1) inhibitor, inhibits au |
| R910265 | BAY-8002 | BAY-8002 is a potent, selective, orally active inhibitor of monocarboxylate tran |
| R910268 | Pentostatin; CI-825; Deoxycoformycin | Pentostatin (CI-825; Deoxycoformycin) is an irreversible inhibitor of adeno |
| R910269 | MC-Val-Cit-PAB | MC-Val-Cit-PAB is a cathepsin cleavable ADC linker that is used for making antib |
| R910270 | HPPH (Synonyms: Photochlor) | HPPH (Photochlor) is a second generation photosensitizer, which acts as a photod |
| R910271 | leniolisib(CDZ 173) | Leniolisib (CDZ173) is a potent and selective PI3Kδ inhibitor currently in phase |
| R910272 | MK677 | CAS NO.：159752-10-0Product Name：MK677Synonyms：MK677EINEC:Molecular Formula：C28H4 |
| R910273 | WST-8 | WST-8 is a water-soluble tetrazolium dye, WST-8 enhances sensitivity of the WST- |
| R910274 | Branebrutinib (Synonyms: BMS-986195) | Branebrutinib (BMS-986195) is a highly potent, selective covalent, irreversible |
| R910276 | Pyridoclax | Pyridoclax is a potential Mcl-1 inhibitor. |
| R910278 | (+/-)-BAY K 8644 | CAS NO.：71145-03-4Product Name：(+/-)-BAY K 8644Synonyms：(+/-)-BAY K 8644EINEC:Mo |
| R910279 | Avadomide (CC 122) | Avadomide (CC 122) is an orally available cereblon modulator. Avadomid |
| R910280 | CCG-203971 | CCG-203971 is a second-generation RhoA/myocardin-related transcription fact |
| R910283 | trabectedin | |
| R910284 | Smurf1-IN-A01 (Synonyms: A01) | Smurf1-IN-A01 (A01) is an ubiquitin ligase Smad ubiquitination regulatory factor |
| R910285 | ML414(NGI-1) | NGI-1 (ML414) is a potent oligosaccharyltransferase (OST) inhibitor, directly ta |
| R910286 | GSK1016790A | GSK1016790A is a potent transient receptor potential vanilloid 4 (TRPV4) activat |
| R910287 | MALT1(inhibitor MI-2) | MALT1 inhibitor MI-2 is a MALT1 inhibitor (IC50=5.84 μM). MALT1 inhibitor MI-2 b |
| R910288 | PF-06700841 P-Tosylate | PF-06700841 P-Tosylate is a potent dual Janus kinase 1 (JAK1) and TYK2 inhibitor |
| R910289 | PF-06700841 | PF-06700841 is a potent dual Janus kinase 1 (JAK1) and TYK2 inhibitor with IC50s |
| R910290 | PZ-2891 | PZ-2891 is an orally bioavailable, brain penetrant pantothenate kinase (PANK) mo |
| R910291 | ZK824859 | ZK824859 (ZK-824859) is a potent, selective urokinase plasminogen activator (uPA |
| R910292 | Fulacimstat (Synonyms: BAY1142524) | Fulacimstat is an orally available chymase inhibitor, with IC50s of 4, 3 nM for |
| R910293 | UCB9608 | UCB9608 is a potent, selective and orally active PI4KIIIβ inhibitor, with an IC5 |
| R910294 | (-)-(S)-B-973B | (-)-(S)-B-973B is a potent allosteric agonist and positive allosteric modulator |
