Products
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 1712293 | 4-methylsulfonyl-2-(trifluoromethyl)benzaldehyde | 1215310-75-0 | >96% | benzaldehyde_1215310-75-0.png) |
| 4-methylsulfonyl-2-(trifluoromethyl)benzaldehyde是一种分子砌块。 | ||||
| 1710163 | MK-8617 | 1187990-87-9 | >98% |  |
| MK-8617 is a potent, selective, orally bioavailabl Pan-Inhibitor of Hypoxia-Inducible | ||||
| 1710135 | MSC2530818 | 1883423-59-3 | >98% |  |
| MSC2530818 is a Potent, Selective, and Orally Bioavailable CDK8 Inhibitor with CDK8 I | ||||
| 1791512 | MDK19922 | 132819-92-2 | 98.0% |  |
| MDK19922, also known as NOD-IN-1 or Compound 4, is a Potent inhibitor of nucleotide-b | ||||
| 179154 | Mozavaptan free base | 137975-06-5 | 98.0% |  |
| Mozavaptan, also known as OPC 31260, is a vasopressin receptor antagonist marketed by | ||||
| 179152 | ML-141 | 71203-35-5 | 98.0% |  |
| ML-141, also known as CID2950007, is a Cdc42 inhibitor (EC50 = 2.1 μM). | ||||
| 179138 | MDK30165 | 2060530-16-5 | 98.0% |  |
| MDK30165, also known as K-Ras(G12C) Inhibitor 6. | ||||
| 20179132 | MMAD | 203849-91-6 | 98.0% |  |
| MMAD, also known as Monomethyl auristatin D, is a highly potent Tubulin inhibitor. MM | ||||
| 179119 | ML-385 | 846557-71-9 | 98.0% |  |
| ML-385 is a potent and selective NRF2 inhibitor (Nrf2; IC50 = 1.9 μM) . ML-385 selec | ||||
| 179115 | ML-277 | 516480-79-8 | 98.0% |  |
| ML-277, also known as Chk2 Inhibitor II, is a Chk2 (checkpoint kinase 2) inhibitor. B | ||||
| 179114 | MDK35833 | 1016535-83-3 | 98.0% |  |
| MDK35833, also known as Oct3/4-inducer-1, is a potent Oct3/4-inducer. MDK35833 can pr | ||||
| 179111 | ML241 HCl | 2070015-13-1 | 98.0% |  |
| ML241 is a potent and selective inhibitors of p97 ATPase. ML241 inhibit p97 ATPase wi | ||||
| 179833 | ML364 | 1991986-30-1 | 98.0% |  |
| ML364 is a small molecule inhibitor of the deubiquitinase USP2 with potential antican | ||||
| 179827 | Mitoxantrone HCl | 70476-82-3 | 98.0% |  |
| Mitoxantrone hydrochloride is the hydrochloride salt of an anthracenedione antibiotic | ||||
| 179826 | ML311 | 315698-17-0 | 98.0% |  |
| ML311, also known as EU-5346, is a potent and selective inhibitor of the Protein-Prot | ||||
| 179810 | ML-18 | 1422269-30-4 | 98.0% |  |
| ML18 is Bombesin receptor subtype 3 (BRS-3) antagonist (IC50 = 4.8 μM). ML-18 inhibi | ||||
| 1781501 | 1-Methylimidazolidine-2,4,5-trione | 3659-97-0 | 98.0% |  |
| 1-MethyliMidazolidine-2,4,5-Trione | ||||
| 16123054 | MK-1064 | 1207253-08-4 | ≧98.0% |  |
| MK-1064 is a potent, selective and orally active Orexin OX2 Receptor Antagonist for p | ||||
| 178908 | MI-503 | 1857417-13-0 | 98.0% |  |
| MI-503 is a potent and selective Menin-MLL inhibitor with IC50 of 14.7 nM. It shows p | ||||
| 178905 | Merestinib (LY2801653) | 1206799-15-6 | 98.0% | -cas-1206799-15-6.png) |
| Merestinib, also known as LY2801653, is a n orally available, small molecule inhibito | ||||
| 2017824 | Miglustat hydrochloride | 210110-90-0 | 98.0% |  |
| Miglustat, also known as OGT 918, is a drug developed by Actelion and is used prima | ||||
| 2017080111 | MK-0812 | 624733-88-6 | 98.0% |  |
| MK-0812 is a potent and selective CCR2 antagonist. Chemokine (C-C motif) receptor 2 ( | ||||
| 201708015 | MONASCIN | 21516-68-7 | 98% |  |
| It is a potent inhibitor of car inogenesis measured against chemical- or UV-initiated | ||||
| 174161 | Mephenytoin | 50-12-4 | 98% | .png) |
| Mephenytoin(CAS 50-12-4) is a hydantoin, used as an anticonvulsant.Mephenytoin(CAS 50 | ||||
| 703301 | MT-DADMe-ImmA | 653592-04-2 | 98% by HNMR/HPLC |  |
| Methylthio-DADMe-immucillin-A (MT-DADMe-ImmA) is an 86-pm inhibitor of human 5-methyl | ||||
| 17031006 | MI-463 | 1628317-18-9 | 98% | |
| MI-463 is a potent inhibitor of Menin-MLL interaction with an IC50 value of 15.3 nM | ||||
| 17030910 | ML-098 | 878978-76-8 | 98% |  |
| ML-098, also known as CID-7345532, is an activator of the GTP-binding protein Rab7 (E | ||||
| 17030804 | ML-265 | 1221186-53-3 | 98% |  |
| ML265 is a potent PKM2 activator induces tetramerization and reduces tumor formation | ||||
| 17030717 | MN-64 | 92831-11-3 | 98% |  |
| MN-64 is a potent and selective inhibitor of Tankyrase 1 and 2 (IC50 = 6 and 72 nM, r | ||||
| 17030714 | ML241 | 1346528-06-0 | 98% |  |
| ML241 is a potent and selective inhibitors of p97 ATPase. ML241 inhibit p97 ATPase wi | ||||