Products
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 25147 | MAT2A-IN-9 ( GSK4362676 ) | 2439277-80-0 | ≧98.0% |  |
| MAT2A-IN-9 ( GSK4362676 ), is a 2-oxoquinazoline derivative, is a potent MAT2A (methi | ||||
| 25143 | MEN-1703 | 2769008-22-0 | 98% Min. |  |
| 25130 | MSC2360844 hemifumarate | 1621688-31-0 | 98% Min. |  |
| 25126 | Maralixibat Chloride | 228113-66-4 | 98% Min. |  |
| Maralixibat (also known as SHP625, LUM001, and lopixibat) is an ileal bile acid trans | ||||
| 25097 | 4-Methyl-1H-indole-2-carbonitrile | 1541530-91-9 | ≧97.0% |  |
| 25090 | Miricorilant | 1400902-13-7 | 98% Min. |  |
| Miricorilant is discontinued. | ||||
| 25073 | MGD-28 | 2991818-13-2 | 98% Min. |  |
| MGD-28 is a potent molecular glue degrader that demonstrates significant in vitro eff | ||||
| 25057 | MFI8 | 694488-83-0 | 98% Min. |  |
| MFI8 is a Mitochondrial Fusion Inhibitor | ||||
| 25039 | MS6105 | 2891709-58-1 | 98% Min. |  |
| 25017 | M3554 | 2763252-25-9 | ≧95.0% |  |
| M3554, a novel anti-GD2 antibody drug conjugate. | ||||
| 25016 | MD-43 | ≧98.0% |  | |
| MD-43 is a potent and selective degrader of MCT4. | ||||
| 24158 | ML-202 | 1221186-52-2 | 98% Min. |  |
| ML-202 is an activator of pyruvate kinase M2 (PKM2). | ||||
| 24151 | ML353 | 2990506-75-5 | 98% Min. |  |
| ML353 is a selective ligand of mGlu5 silent allosteric modulator (SAM). | ||||
| 24150 | MIF098 | 1208448-95-6 | 98% Min. |  |
| MIF098 is a macrophage migration inhibitory factor (MIF) antagonist. | ||||
| 24129 | 2-MNG | 2101538-28-5 | ≧98.0% |  |
| 2-MNG is a new potent melanogenesis inhibitor, which exhibits a unique mode of action | ||||
| 24124 | Mevrometostatum | 1844849-10-0 | 98% Min. |  |
| Mevrometostatum is an enhancer of zeste homolog 2 (EZH2) inhibitor. | ||||
| 24044 | 3-(methylsulfonyl)propanenitrile | 54863-37-5 | 98% Min. | propanenitrile_54863-37-5.png) |
| Dapansutrile is a potent, orally active and selectiveNLRP3inflammasome inhibitor. Dap | ||||
| 20675 | Mavoglurant | 543906-09-8 | 98% Min. |  |
| 262401 | MRTX1719 | 2630904-45-7 | ≧96.0% | |
| MRTX1719 is a potent and selective binder to the PRMT5•MTA complex and selectively | ||||
| 20615 | Mavodelpar | 942594-93-6 | 98% Min. |  |
| Mavodelpar is a peroxisome proliferator activated receptor (PPAR) delta agonist. | ||||
| 20611 | MRTX849 | 2326521-71-3 | 98% Min. |  |
| Adagrasib, also known as MRTX849, is a potent, highly selective, oral available KRAS | ||||
| 20592 | Migoprotafib | 2377352-49-1 | 98% Min. |  |
| Migoprotafib, also known as GDC-1971 and RLY-1971, is a SHP2 allosteric inhibitor. GD | ||||
| 20572 | Mtb-IN-2 | 2861190-30-7 | 98% Min. |  |
| Mtb-IN-2 (compound 10c) is an antimicrobial agent against Mycobacterium tuberculosis | ||||
| 20542 | MBX-8025 lysine anhydrous | 928821-41-4 | 98% Min. |  |
| MBX-8025 lysine anhydrous is a selective PPAR-delta agonist. | ||||
| 20529 | Milademetan free base | 1398568-47-2 | 98% Min. |  |
| Milademetan, also known as DS-3032b or DS-3032, is a potent and selective MDM2 inhibi | ||||
| 20528 | muvalaplin | 2565656-70-2 | 98% Min. |  |
| 20503 | MK-8189 | 1424371-93-6 | 98% Min. |  |
| MK-8189 is a Highly Potent and Selective PDE10A Inhibitor for the Treatment of Schizo | ||||
| 20470 | MCUF-651 | 2747162-85-0 | 98% Min. |  |
| MCUF-651 is a small molecule guanylyl cyclase A receptor positive allosteric modulato | ||||
| 20466 | Moracin C | 69120-06-5 | 98% Min. |  |
| Moracin C is a phenolic compound isolated from Artocarpus heterophyllus. Moracin C su | ||||
| 20464 | ML192 | 460331-61-7 | 98% Min. |  |
| ML192, also known as MLS000526305 and CID1434953, is a selective ligands for GPR55. T | ||||