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Cas Index 1

• 1421373-62-7 | MDK3627 (Catalog# : 187161)MDK3627, also known as Mutant EGFR inhibitor, is a selective and potent Mutated EGFR
• 1303607-07-9 | MI-773 (Catalog# : 185251)MI-773 is a novel orally available MDM2 antagonist.
• 1417997-93-3 | MDK-7933 (Catalog# : 184161)MDK-7933, also known as HDAC8-IN-1, is a HDAC8 inhibitor with an IC50 of 27.2 nM in c
• 1448189-80-7 | MDK7526 HCl (Catalog# : 184104)MDK7526, also known as VHL Ligand 1; Protein degrader 1, is a potent and selective pr
• 1190379-70-4 | MRT68921 (Catalog# : 184103)MRT68921 is an inhibitor of ULK1 and ULK2 (IC50s = 2.9 and 1.1 nM, respectively).
• 1870916-87-2 | Mc-Val-Ala-PAB (Catalog# : 184219)Mc-Val-Ala-PAB is a useful linker to make antibody-drug-conjugate (ADC) for targeting
• 111797-22-9 | MDK7229 (Catalog# : 184211)MDK7229，也称为MD2- IN -1是MD2(髓样分化蛋白2)抑制剂。MDK7229锁住LPS-
• 1215310-75-0 | 4-methylsulfonyl-2-(trifluoromethyl)benzaldehyde (Catalog# : 1712293)4-methylsulfonyl-2-(trifluoromethyl)benzaldehyde是一种分子砌块。
• 1187990-87-9 | MK-8617 (Catalog# : 1710163)MK-8617 is a potent, selective, orally bioavailabl Pan-Inhibitor of Hypoxia-Inducible
• 1883423-59-3 | MSC2530818 (Catalog# : 1710135)MSC2530818 is a Potent, Selective, and Orally Bioavailable CDK8 Inhibitor with CDK8 I
• 132819-92-2 | MDK19922 (Catalog# : 1791512)MDK19922, also known as NOD-IN-1 or Compound 4, is a Potent inhibitor of nucleotide-b
• 137975-06-5 | Mozavaptan free base (Catalog# : 179154)Mozavaptan, also known as OPC 31260, is a vasopressin receptor antagonist marketed by
• 1016535-83-3 | MDK35833 (Catalog# : 179114)MDK35833, also known as Oct3/4-inducer-1, is a potent Oct3/4-inducer. MDK35833 can pr
• 1991986-30-1 | ML364 (Catalog# : 179833)ML364 is a small molecule inhibitor of the deubiquitinase USP2 with potential antican
• 1422269-30-4 | ML-18 (Catalog# : 179810)ML18 is Bombesin receptor subtype 3 (BRS-3) antagonist (IC50 = 4.8 μM). ML-18 inhibi
• 1207253-08-4 | MK-1064 (Catalog# : 16123054)MK-1064 is a potent, selective and orally active Orexin OX2 Receptor Antagonist for p
• 1857417-13-0 | MI-503 (Catalog# : 178908)MI-503 is a potent and selective Menin-MLL inhibitor with IC50 of 14.7 nM. It shows p
• 1206799-15-6 | Merestinib (LY2801653) (Catalog# : 178905)Merestinib, also known as LY2801653, is a n orally available, small molecule inhibito
• 1628317-18-9 | MI-463 (Catalog# : 17031006)MI-463 is a potent inhibitor of Menin-MLL interaction with an IC50 value of 15.3 nM
• 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