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Cas Index 1

• 1219737-12-8 | MK-3903 (Catalog# : 192183)MK-3903 is a potent and selective AMPK activator (EC50 = 8 nM).
• 1049704-18-8 | MA242 TFA (Catalog# : 191256)MA242 is a Dual Inhibitors of MDM2 and NFAT1 for Pancreatic Cancer Therapy. MA242 dec
• 1799631-75-6 | MIK665 (Catalog# : 191252)MIK665, also known as S 64315, is an inhibitor of induced myeloid leukemia cell diffe
• 183721-13-3 | MRS1177 (Catalog# : 1812296)MRS1177 is a bioactive chemical.
• 1642288-47-8 | Mavacamten (Catalog# : 181255)Mavacamten, also known as SAR-439152 and MYK-461, is a myosin inhibitor potentially f
• 147116-67-4 | Maropitant (Catalog# : 1811261)Maropitan, also known as CJ 11972, is a neurokinin (NK1) receptor antagonist.
• 183721-15-5 | MRS1220 (Catalog# : 1810228)MRS1220 is a potent and highly selective antagonist at the human A3 adenosine recepto
• 1445251-22-8 | ME0328 (Catalog# : 1810174)ME0328 is an inhibitor of PARP-3 (IC50 = 0.89 μM).
• 1908414-82-3 | MDK-4823 (Catalog# : 18962)MDK-4823, also known as LMPTP inhibitor1; is a potent inhibitor of the low-molecular-
• 1644342-14-2 | ML-792 (Catalog# : 18941)ML-792 is a potent and selective SAE inhibitor with nanomolar potency in cellular ass
• 1883510-31-3 | ML327 (Catalog# : 187162)ML327 is a blocker of MYC. ML327 mediated transcriptional de-repression of E-cadherin
• 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