Products
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 16122796 | MPTP hydrochloride | 23007-85-4 | 98% |  |
| MPTP hydrochloride is a dopaminergic neurotoxin and cause selective destruction of do | ||||
| 16122790 | ML323 | 1572414-83-5 | 98% |  |
| ML323 is a highly potent and selective USP1-UAF1 inhibitor with IC50 of 76 nM.ML323 i | ||||
| 16122749 | ML390 | 2029049-79-2 | 98% |  |
| ML390 is a human DHODH inhibitor that induces differentiation in acute myeloid leukem | ||||
| 16122745 | MRT67307 | 1190378-57-4 | 98% |  |
| MRT67307 is a potent and dual IKKϵ and TBK1 inhibitor with IC50 of 160 and 19 nM, re | ||||
| 16122717 | MK-4827(Niraparib) tosylate | 1038915-73-9 | 98% | |
| MK-4827(Niraparib) tosylate is a selective inhibitor of PARP1/PARP2 with IC50 of 3.8 | ||||
| 6111524 | MP-A08 | 219832-49-2 | 98% | |
| MP-A08 is a highly selective ATP competitive SK inhibitor that targets both SK1 and S | ||||
| 6111404 | Mcl1-IN-2 | 292057-76-2 | 98% | |
| Mcl1-IN-2 is a Mcl-1 inhibitor without reported IC50 value. | ||||
| 6111403 | Marinopyrrole A | 1227962-62-0 | 98% | |
| Marinopyrrole (Maritoclax) is a novel and specific Mcl-1 inhibitor with an IC50 value | ||||
| 61116 | ML224 | 1338824-21-7 | 98% | |
| ML224(NCGC00242364; ANTAG3) is a selective TSHR inverse agonist; inhibits TSH-stimula | ||||
| 61114 | (±)-Methotrimeprazine D6 | 1189805-51-3 | 98% | |
| ()-Methotrimeprazine (D6) is the deuterium labeled Methotrimeprazine, which is a D3 d | ||||
| 6111017 | Motolimod | 926927-61-9 | 98% | |
| Motolimod | ||||
| 6111014 | MCC950 sodium | 256373-96-3 | 98% |  |
| MCC950 (CP 456773) sodium is a potent, selective, small molecule inhibitor of NLRP3 w | ||||
| 6111012 | MS023 | 1831110-54-3 | 98% | |
| MS023 is a potent, selective, and cell-active inhibitor of human type I PRMTs with IC | ||||
| 6111008 | MK-4101 | 935273-79-3 | 98% | |
| MK-4101 is a potent SMO Inhibitor of the Hedgehog PathwayMK-4101 is a potent SMO Inhi | ||||
| 611940 | ML346 | 100872-83-1 | 98% | |
| ML346 is a novel activator of Hsp70 with EC50 of 4600 nM in HeLa cell toxicity assay. | ||||
| 611820 | mTOR-IN-1 | 1207358-59-5 | 98% | |
| mTOR-IN-1 is a potent and selective ATP-competitive inhibitor of mTOR with Ki of 1.5 | ||||
| 161009023 | Miltefosine | 58066-85-6 | 98% by HPLC |  |
| Miltefosine targets cellular membranes, modulating cell membrane permeability, membra | ||||
| 169701 | 1-METHYL-5-NITRO-1H-INDOLE | 29906-67-0 | 98% by HNMR/HPLC |  |
| 1-METHYL-5-NITRO-1H-INDOLE CAS#29906-67-0 | ||||
| 16071022 | Mubritinib | 366017-09-6 | 98% by HPLC |  |
| Mubritinib, also known as TAK-165, is a protein kinase inhibitor which was under deve | ||||
| 16070814 | MK-8245 | 1030612-87-3 | 98% by HPLC |  |
| MK-8245 | ||||
| 16070813 | MLN120B | 783348-36-7 | 98% by HPLC |  |
| MLN120B | ||||
| 16070106 | MS417 | 916489-36-6 | 98% by HPLC |  |
| MS417, also known as GTPL7512, is a potent and selective BRD4 inhibitor. MS417 inhibi | ||||
| 16062901 | Molidustat (BAY85-3934) | 1154025-82-6 | 98% by HPLC | |
| Molidustat (BAY85-3934) | ||||
| 1662118 | MK-8931 ( Verubecestat ) | 1286770-55-5 | 98% by HPLC/HNMR | -cas-1286770-55-5.png) |
| Verubecestat(MK-8931) is a small-molecule inhibitor of beta-secretase cleaving enzyme | ||||
| 16062101 | Methyl 2,5-dimethylnicotinate | 63820-72-4 | 98% by HPLC |  |
| Methyl 2,5-dimethylnicotinate | ||||
| 16060603 | MDK-5220 | 1796565-52-0 | 98% by HPLC |  |
| MDK-5220 exhibits an orexin agonist activity and is expected to be useful as an excel | ||||
| 032514 | MK-5172 | 1350514-68-9 | 98% |  |
| Coming soon! | ||||
| 030904 | Mirodenafil | 862189-95-5 | 98% |  |
| Coming soon! | ||||
| 030901 | MK-2866 | 1202044-20-9 | 98% |  |
| Coming soon! | ||||
| 030101 | MCC950 | 210826-40-7 | 98% |  |
| MCC950 is a potent, selective, small-molecule inhibitor of NLRP3 with IC50 of 7.5 nM | ||||