Products
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 184191 | MDK-1699 | 432001-69-9 | >98% |  |
| MDK-1699, also known as Skp2 inhibitor C1 and SKPin C1, is a Skp2 inhibitor. | ||||
| 184173 | MDK-6149 | 508186-14-9 | >98% |  |
| MDK-6149, also known as ACSS2 Inhibitor or Ac-CoA Synthase Inhibitor I, is a Ac-CoA S | ||||
| 184161 | MDK-7933 | 1417997-93-3 | >98% |  |
| MDK-7933, also known as HDAC8-IN-1, is a HDAC8 inhibitor with an IC50 of 27.2 nM in c | ||||
| 184104 | MDK7526 HCl | 1448189-80-7 | >98% |  |
| MDK7526, also known as VHL Ligand 1; Protein degrader 1, is a potent and selective pr | ||||
| 184103 | MRT68921 | 1190379-70-4 | >98% |  |
| MRT68921 is an inhibitor of ULK1 and ULK2 (IC50s = 2.9 and 1.1 nM, respectively). | ||||
| 184102 | MRT68921 HCl | 2080306-21-2 | >98% |  |
| MRT68921 is an inhibitor of ULK1 and ULK2 (IC50s = 2.9 and 1.1 nM, respectively). | ||||
| 184219 | Mc-Val-Ala-PAB | 1870916-87-2 | >98% |  |
| Mc-Val-Ala-PAB is a useful linker to make antibody-drug-conjugate (ADC) for targeting | ||||
| 184216 | ML335 | 825658-06-8 | >98% |  |
| ML335是一种有效的、选择性的TREK-1/2激活剂。ML335是一种用于OPRM1-O | ||||
| 184215 | ML365 | 947914-18-3 | >98% |  |
| ML365是一种有效的、选择性的K2P3.1 TASK-1通道阻滞剂。 | ||||
| 184211 | MDK7229 | 111797-22-9 | >98% |  |
| MDK7229，也称为MD2- IN -1是MD2(髓样分化蛋白2)抑制剂。MDK7229锁住LPS- | ||||
| 18422 | ML204盐酸盐 | 2070015-10-8 | >98% |  |
| ML204是一种新型的、潜在的TRPC4通道抑制剂。ML204是研究TRPC4通道功 | ||||
| 18421 | MDK6574 | 2102196-57-4 | >98% |  |
| MDK6574, also known as FAA1 agonist-1, is a FAA1 agonist. | ||||
| 183131 | 2-Methyl-7-azaindole | 23612-48-8 | >96% |  |
| 2-Methyl-7-azaindole is a drug Intermediate. | ||||
| 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 | ||||