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| Cat.No. | Product name | Product Description |
| RH131554 | Tyrosinase-IN-2 | Tyrosinase-IN-2 (compound 67) is a potent inhibitor of tyrosinase. Tyrosinase is |
| RH131555 | Resorcinolnaphthalein | Resorcinolnaphthalein is a specific angiotensin-converting enzyme 2 (ACE2) |
| RH131556 | 4-(N-(1,8-萘酰亚胺))-N-丁酸 | Virstatin inhibits the pili system synthesis and prevents A. baumannii biofilm f |
| RH131557 | Hepln-13 | Hepln-13 is a potent and orally active Hepsin inhibitor with an IC50 of 0.33 µM. |
| RH131558 | 硫酸盐离子载体I | sulfate-ionophore i |
| RH131559 | NSC756093 | NSC756093 |
| RH131560 | M-31850 | M-31850 is a potent, selective and competitive β-hexosaminidase (Hex) inhibitor |
| RH131561 | FQ | FQ is a tyrosinase inhibitor that effectively inhibits the diphenolase activity |
| RH131562 | Difluorinated Curcumin(3,4-Difluorobenzylidene curcumin) | Difluorinated Curcumin (3,4-Difluorobenzylidene curcumin) is a fluorinated curcu |
| RH131564 | Z-LEED-FMK | Z-LEED-FMK is a caspase-13 and caspase-4 inhibitor. Z-LEED-FMK also inhibits cas |
| RH131565 | Z-LEVD-FMK | Z-LEVD-FMK is a cell-permeable caspase-4 inhibitor. Z-LEVD-FMK blocks ER stress- |
| RH131566 | Z-LEHD-FMK | Z-LEHD-FMK is a selective and irreversible inhibitor of caspase-9, protects agai |
| RH131567 | Z-LETD-FMK | Z-Leu-Glu(OMe)-Thr-DL-Asp(OMe)-fluoromethylketone |
| RH131568 | (3S)-3-[[叔丁氧羰基]氨基]-5-氟-4-氧代-戊酸甲酯 | Boc-Asp(OME)-Fluoromethyl Ketone is a broad range caspase inhibitor that inhibit |
| RH131569 | Z-VEID-FMK | Z-VEID-FMK (Z-VE(OMe)ID(OMe)-FMK) is a selective and irreversible caspase-6 |
| RH131570 | CA-074（OH） | CA-074 is a potent inhibitor of cathepsin B with a Ki of 2 to 5 nM. |
| RH131571 | PD-1-IN-17 | PD-1-IN-17 is a programmed cell death-1 (PD-1) inhibitor extracted from patent W |
| RH131572 | Z-FG-NHO-BzOMe | Z-FG-NHO-BzOME is a cysteine protease inhibitor that selectively inhibits cathep |
| RH131573 | PSB-1115 | PSB-1115 is a selective A2B Adenosine Receptor antagonist. PSB-1115 inhibits the |
| RH131574 | VK-2019 | VK-2019 is an oral active, selective EBNA1((Epstein-Barr Nuclear Antigen 1) inhi |
| RH131575 | BSJ-03-204 | BSJ-03-204 is a PROTAC connected by ligands for Cereblon and CDK. BSJ-03-204 is |
| RH131576 | SRX3177 | SRX3177 is a triple inhibitor of CDK4/6, PI3K, and BRD4, with IC50s of 33 nM (BR |
| RH131578 | PE154 | PE154 (Compound 13) is a potent fluorescent inhibitor of human acetylcholinester |
| RH131579 | IT1t dihydrochloride | IT1t dihydrochloride is a potent CXCR4 antagonist; inhibits CXCL12/CXCR4 interac |
| RH131580 | Lobeglitazone sulfate | Lobeglitazone sulfate is a new type of thiazolidinedione. Lobeglitazone sulfate |
