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| Cat.No. | Product name | Product Description |
| R2053455 | VU0119498 | VU0119498 is an agonist of M1 muscarinic receptor with EC50 of 3.1 μM. VU0119498 |
| R2053456 | X-115(Ewha-18278) | APX-115 free base (Ewha-18278 free base) is a potent, orally active pan NADPH ox |
| R2053457 | LC3-mHTT-IN-AN1 (Compound AN1) | LC3-mHTT-IN-AN1 (Compound AN1) is a mHTT-LC3 linker compound, which interacts wi |
| R2053458 | VU0238429 | VU 0238429 is positive allosteric modulator of muscarinic acetylcholine receptor |
| R2053459 | XP-59 | XP-59 is a potent inhibitor of the SARS-CoV Mpro, with a Ki of 0.1 μM. |
| R2053460 | BETd-260(ZBC 260) | BETd-260 (ZBC 260) is a potent PROTAC BET degrader, with as low as 30 pM against |
| R2053461 | AP20187 (B/B Homodimerizer) | AP20187 (B/B Homodimerizer) is a cell-permeable ligand used to dimerize FK506-bi |
| R2053462 | Dapoxetine | Dapoxetine is a short-acting novel selective serotonin reuptake inhibitor(SSRI). |
| R2053463 | Dapoxetine Hydrochloride | CAS NO.：129938-20-1Product Name：Dapoxetine HydrochlorideSynonyms：Dapoxetine Hydr |
| R2053464 | JBJ-04-125-02 | JBJ-04-125-02 is a potent, mutant-selective, allosteric and orally active EGFR i |
| R2053465 | BAY885 | BAY885 is a novel ERK5 inhibitor. |
| R2053466 | Pemigatinib(INCB054828) | Pemigatinib (INCB054828) is an orally active, selective FGFR inhibitor with IC50 |
| R2053467 | TLX agonist 1 | TLX agonist 1 (ccrp2) is an orphan nuclear receptor tailless (TLX, NR2E1) modula |
| R2053468 | HEOWNS | |
| R2053469 | CIL62 | CIL62 is a caspase-3/7-independent cell death inducer. The mechanism of action o |
| R2053470 | AMG-510;AMG510 | AMG-510 is a first-in-class, orally bioavailable, and selective KRAS G12C covale |
| R2053472 | WRG-28 | WRG-28 is a selective, extracellularly acting DDR2 allosteric inhibitor with an |
| R2053473 | MZ1 | MZ 1 is a PROTAC BRD4 degrader. MZ 1 potently and rapidly induces reversible, lo |
| R2053474 | glucosyringic acid | |
| R2053475 | Isochlorogenic acid A | Isochlorogenic acid A (3,5-Dicaffeoylquinic acid) is a natural phenolic acid wit |
| R2053476 | TNO155 | TNO155 is a potent selective and orally active allosteric inhibitor of wild-type |
| R2053477 | Filastatin | Filastatin is a long-lasting inhibitor of Candida albicans filamentation. Filast |
| R2053478 | ABT-492 Meglumine;Delafloxacin meglumine | Delafloxacin meglumine (ABT492 meglumine; RX-3341 meglumine; WQ-3034 meglumine) |
| R2053479 | ZN2007-RM1 | |
| R2053482 | MAX-40279 | MAX-40279 hydrochloride is a dual and potent inhibitor of FLT3 kinase |
