Products
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 1811282 | ML 351 | 847163-28-4 | >98% |  |
| ML 351 is a selective 12/15 LOX inhibitor that is active in vivo. | ||||
| 1811261 | Maropitant | 147116-67-4 | >98% |  |
| Maropitan, also known as CJ 11972, is a neurokinin (NK1) receptor antagonist. | ||||
| 181152 | MBQ-167 | 2097938-73-1 | >98% |  |
| MBQ-167 is a potent, dual Rac/Cdc42 inhibitor with IC50 of 103/78 nM, respectively, i | ||||
| 1810301 | MDK4882 | 94164-88-2 | >98% |  |
| MDK4882 also known as PKM2 inhibitor or compound 3k, is a PKM2 inhibitor. | ||||
| 181022 | MU-380 | 2109805-78-7 | >98% |  |
| MU-380 is a potent and selective CHK1 inhibitor. | ||||
| 1810228 | MRS1220 | 183721-15-5 | >98% |  |
| MRS1220 is a potent and highly selective antagonist at the human A3 adenosine recepto | ||||
| 1810174 | ME0328 | 1445251-22-8 | >98% |  |
| ME0328 is an inhibitor of PARP-3 (IC50 = 0.89 μM). | ||||
| 18962 | MDK-4823 | 1908414-82-3 | >98% |  |
| MDK-4823, also known as LMPTP inhibitor1; is a potent inhibitor of the low-molecular- | ||||
| 18961 | MDK-4774 | 2036044-77-4 | >98% |  |
| MDK-4774, Porcupine-IN-1, is a Porcupine inhibitor. | ||||
| 18941 | ML-792 | 1644342-14-2 | >98% |  |
| ML-792 is a potent and selective SAE inhibitor with nanomolar potency in cellular ass | ||||
| 187162 | ML327 | 1883510-31-3 | >98% |  |
| ML327 is a blocker of MYC. ML327 mediated transcriptional de-repression of E-cadherin | ||||
| 187161 | MDK3627 | 1421373-62-7 | >98% |  |
| MDK3627, also known as Mutant EGFR inhibitor, is a selective and potent Mutated EGFR | ||||
| 18742 | MLN8054 | 869363-13-3 | >98% |  |
| MLN8054 is an aurora kinase inhibitor MLN8054, which is an orally bioavailable, highl | ||||
| 185284 | MK-3207 | 957118-49-9 | >98% |  |
| MK-3207 is a potent and orally active calcitonin gene-related peptide receptor antago | ||||
| 185251 | MI-773 | 1303607-07-9 | >98% |  |
| MI-773 is a novel orally available MDM2 antagonist. | ||||
| 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- | ||||
| 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 | ||||