产品目录
| 编号 | 化学名称 | Cas号 | 纯度 | 化学结构 |
|---|---|---|---|---|
| 17022403 | 单甲基奥立斯丁 | 474645-27-7 | 98% | -cas-474645-27-7.png) |
| MMAE，又称单甲基奥立斯丁，是一种合成的抗肿瘤药物。 | ||||
| 17021322 | Monastrol | 329689-23-8 | 98% |  |
| Monastrol是一种细胞可渗透的小分子抑制剂，它对保持半纺锤的分离 | ||||
| 17021313 | MS049 | 1502816-23-0 | 98% | |
| MS049是PRMT4和PRMT6的一种有效的选择性抑制剂，IC50分别为34 nM和43 n | ||||
| 17021301 | Miransertib(ARQ 092) | 1313883-00-9 | 98% | -cas-1313883-00-9.png) |
| ARQ 092是一种新型的口服生物可用性和选择性AKT通路抑制剂，在晚 | ||||
| 712101 | MT-DADMe-ImmA(MTDIA HCl) | 1399840-35-7 | 98% | -cas-1399840-35-7.png) |
| MT-DADMe-ImmA(MTDIA盐酸盐)是一种新型的MTAP抑制剂，具有治疗头颈部和 | ||||
| 17011908 | 7-Methyl-7H-pyrrolo[2,3-d]pyriMidin-4-aMine | 7752-54-7 | 98% |  |
| 7-Methyl-7H-pyrrolo[2,3-d]pyriMidin-4-aMine | ||||
| 17011107 | ML-7 | 110448-33-4 | 98% |  |
| ML-7是平滑肌肌球蛋白轻链激酶的抑制剂(MLCK)，Ki值为0.3μM。 | ||||
| 17011105 | MX69 | 1005264-47-0 | 98% | |
| MX69是一种MDM2/XIAP抑制剂, 用于治疗癌症。 | ||||
| 16123055 | MK-571 sodium salt | 115104-28-4 | 98% |  |
| MK-571 is a selective, orally active CysLT1 receptor antagonist. It blocks the bindin | ||||
| 16123053 | Mizoribine | 50924-49-7 | 98% |  |
| Mizoribine,Mizoribine (INN, trade name Bredinin) is an immunosuppressive drug. The co | ||||
| 16123052 | Mivebresib | 1445993-26-9 | 98% |  |
| Mivebresib, also known as ABBV-075, is a potent BET inhibitor (bromodomain (BRD)-cont | ||||
| 16123051 | Mitoxantrone HCl | 65271-80-9 | 98% |  |
| Mitoxantrone hydrochloride is the hydrochloride salt of an anthracenedione antibiotic | ||||
| 16123049 | Mirin | 1198097-97-0 | 98% |  |
| Mirin is a Mre11-Rad50-Nbs1 (MRN)-ATM pathway inhibitor. | ||||
| 16123048 | Migalastat HCl | 75172-81-5 | 98% |  |
| Migalastat HCl, also known as AT1001 or GR181413A, is a pharmacological chaperone tha | ||||
| 16123047 | MI-2 (MALT1 inhibitor) | 1047953-91-2 | 98% | |
| MI-2 is a MALT1 inhibitor (IC50 = 5.84 M). MI-2 binds directly to MALT1 and irreversi | ||||
| 16123046 | MG-101 | 110044-82-1 | 98% |  |
| MG-101, also known as Calpain Inhibitor I and ALLN, is a calpain inhibitor (IC50 = 0. | ||||
| 16123045 | Mertansine (DM1) | 139504-50-0 | 98% | |
| Mertansine refers to the thiol-containing maytansinoid, DM1 (N2-deacetyl-N2-(3-mercap | ||||
| 16122832 | MC-976 | 129831-99-8 | 98% | |
| MC-976 is an Vitamin D3 derivative. | ||||
| 16122831 | Mafodotin | 863971-19-1 | 98% | |
| Mafodotin, also known as mc-MMAF and SGD-1269 or Maleimidocaproyl monomethylauristati | ||||
| 16122830 | Madrasin | 374913-63-0 | 98% | |
| Madrasin is a potent and cell penetrant splicing inhibitor that interferes with the e | ||||
| 16122829 | M2I-1 | 312271-03-7 | 98% | |
| M2I-1, also known as Mad2 Inhibitor-1, is Protein-Protein Interaction Inhibitor Targe | ||||
| 161227105 | MK571 | 115103-85-0 | 98% | |
| MK-571 is a selective, orally active CysLT1 receptor(Cysteinyl leukotriene receptor) | ||||
| 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 | ||||