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Cas Index 1

• 1221186-53-3 | ML-265 (Catalog# : 17030804)ML265 is a potent PKM2 activator induces tetramerization and reduces tumor formation
• 1346528-06-0 | ML241 (Catalog# : 17030714)ML241 is a potent and selective inhibitors of p97 ATPase. ML241 inhibit p97 ATPase wi
• 198821-22-6 | Merimepodib (Catalog# : 17030308)Merimepodib, also known as VX-497, is orally bioavailable IMPDH inhibitor, which inhi
• 1550008-55-3 | ML-264 (Catalog# : 17030302)ML-264 is a Krppel-like factor 5 (KLF5) inhibitor That Potently Inhibits Growth of Co
• 1030612-90-8 | MK-8245 (Catalog# : 17030109)MK-8245 is a potent, liver-targeted SCD inhibitor with preclinical antidiabetic and a
• 1268454-23-4 | MLN-1117 (Catalog# : 17030101)Serabelisib (also known as MLN1117, INK1117, and TAK-117) is an orally bioavailable i
• 1404437-62-2 | ML-281 (Catalog# : 17022811)ML-281 is a potent ans selective STK33 inhibitor (IC50 = 14 nM). ML281 showed low nan
• 1502816-23-0 | MS049 (Catalog# : 17021313)MS049 is a potent and selective inhibitor of PRMT4 and PRMT6 with IC50s of 34 nM
• 1313883-00-9 | Miransertib(ARQ 092) (Catalog# : 17021301)ARQ 092 is a novel, orally bioavailable and selective AKT pathway inhibitor exhibit
• 1399840-35-7 | MT-DADMe-ImmA(MTDIA HCl) (Catalog# : 712101)Methylthio-DADMe-immucillin-A (MT-DADMe-ImmA) is an 86-pm inhibitor of human 5-methyl
• 110448-33-4 | ML-7 (Catalog# : 17011107)ML-7 is an inhibitor of smooth muscle myosin light chain kinase (MLCK) with a Ki 
• 1005264-47-0 | MX69 (Catalog# : 17011105)MX69 is a MDM2/XIAP inhibitor, used for cancer treatment. 
• 115104-28-4 | MK-571 sodium salt (Catalog# : 16123055)MK-571 is a selective, orally active CysLT1 receptor antagonist. It blocks the bindin
• 1445993-26-9 | Mivebresib (Catalog# : 16123052)Mivebresib, also known as ABBV-075, is a potent BET inhibitor (bromodomain (BRD)-cont
• 1198097-97-0 | Mirin (Catalog# : 16123049)Mirin is a Mre11-Rad50-Nbs1 (MRN)-ATM pathway inhibitor.
• 1047953-91-2 | MI-2 (MALT1 inhibitor) (Catalog# : 16123047)MI-2 is a MALT1 inhibitor (IC50 = 5.84 M). MI-2 binds directly to MALT1 and irreversi
• 110044-82-1 | MG-101 (Catalog# : 16123046)MG-101, also known as Calpain Inhibitor I and ALLN, is a calpain inhibitor (IC50 = 0.
• 139504-50-0 | Mertansine (DM1) (Catalog# : 16123045)Mertansine refers to the thiol-containing maytansinoid, DM1 (N2-deacetyl-N2-(3-mercap
• 129831-99-8 | MC-976 (Catalog# : 16122832)MC-976 is an Vitamin D3 derivative.
• 115103-85-0 | MK571 (Catalog# : 161227105)MK-571 is a selective, orally active CysLT1 receptor(Cysteinyl leukotriene receptor)
• 1572414-83-5 | ML323 (Catalog# : 16122790)ML323 is a highly potent and selective USP1-UAF1 inhibitor with IC50 of 76 nM.ML323 i
• 1190378-57-4 | MRT67307 (Catalog# : 16122745)MRT67307 is a potent and dual IKKϵ and TBK1 inhibitor with IC50 of 160 and 19 nM, re
• 1038915-73-9 | MK-4827(Niraparib) tosylate (Catalog# : 16122717)MK-4827(Niraparib) tosylate is a selective inhibitor of PARP1/PARP2 with IC50 of 3.8
• 1227962-62-0 | Marinopyrrole A (Catalog# : 6111403)Marinopyrrole (Maritoclax) is a novel and specific Mcl-1 inhibitor with an IC50 value
• 1338824-21-7 | ML224 (Catalog# : 61116)ML224(NCGC00242364; ANTAG3) is a selective TSHR inverse agonist; inhibits TSH-stimula
• 1189805-51-3 | (±)-Methotrimeprazine D6 (Catalog# : 61114)()-Methotrimeprazine (D6) is the deuterium labeled Methotrimeprazine, which is a D3 d
• 1831110-54-3 | MS023 (Catalog# : 6111012)MS023 is a potent, selective, and cell-active inhibitor of human type I PRMTs with IC
• 100872-83-1 | ML346 (Catalog# : 611940)ML346 is a novel activator of Hsp70 with EC50 of 4600 nM in HeLa cell toxicity assay.
• 1207358-59-5 | mTOR-IN-1 (Catalog# : 611820)mTOR-IN-1 is a potent and selective ATP-competitive inhibitor of mTOR with Ki of 1.5
• 1030612-87-3 | MK-8245 (Catalog# : 16070814)MK-8245