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Products

Catalog NoChemical NameCAS NumberPurityChemical Structure
1791512MDK19922132819-92-298.0%
MDK19922, also known as NOD-IN-1 or Compound 4, is a Potent inhibitor of nucleotide-b
179154Mozavaptan free base137975-06-598.0%
Mozavaptan, also known as OPC 31260, is a vasopressin receptor antagonist marketed by
179152ML-14171203-35-598.0%
ML-141, also known as CID2950007, is a Cdc42 inhibitor (EC50 = 2.1 μM).
179138MDK301652060530-16-598.0%
MDK30165, also known as K-Ras(G12C) Inhibitor 6.
20179132MMAD203849-91-698.0%
MMAD, also known as Monomethyl auristatin D, is a highly potent Tubulin inhibitor. MM
179119ML-385846557-71-998.0%
ML-385 is a potent and selective NRF2 inhibitor (Nrf2; IC50 = 1.9 μM) . ML-385 selec
179115ML-277516480-79-898.0%
ML-277, also known as Chk2 Inhibitor II, is a Chk2 (checkpoint kinase 2) inhibitor. B
179114MDK358331016535-83-398.0%
MDK35833, also known as Oct3/4-inducer-1, is a potent Oct3/4-inducer. MDK35833 can pr
179111ML241 HCl2070015-13-198.0%
ML241 is a potent and selective inhibitors of p97 ATPase. ML241 inhibit p97 ATPase wi
179833ML3641991986-30-198.0%
ML364 is a small molecule inhibitor of the deubiquitinase USP2 with potential antican
179827Mitoxantrone HCl70476-82-398.0%
Mitoxantrone hydrochloride is the hydrochloride salt of an anthracenedione antibiotic
179826ML311315698-17-098.0%
ML311, also known as EU-5346, is a potent and selective inhibitor of the Protein-Prot
179810ML-181422269-30-498.0%
ML18 is Bombesin receptor subtype 3 (BRS-3) antagonist (IC50 = 4.8 μM). ML-18 inhibi
17815011-Methylimidazolidine-2,4,5-trione3659-97-098.0% 
1-MethyliMidazolidine-2,4,5-Trione 
16123054MK-10641207253-08-4≧98.0%
MK-1064 is a potent, selective and orally active Orexin OX2 Receptor Antagonist for p
178908MI-5031857417-13-098.0% 
MI-503 is a potent and selective Menin-MLL inhibitor with IC50 of 14.7 nM. It shows p
178905Merestinib (LY2801653)1206799-15-698.0% 
Merestinib, also known as LY2801653, is a n orally available, small molecule inhibito
2017824Miglustat hydrochloride210110-90-098.0% 
 Miglustat, also known as OGT 918, is a drug developed by Actelion and is used prima
2017080111MK-0812624733-88-698.0% 
MK-0812 is a potent and selective CCR2 antagonist. Chemokine (C-C motif) receptor 2 (
201708015MONASCIN21516-68-798% 
It is a potent inhibitor of car inogenesis measured against chemical- or UV-initiated
174161Mephenytoin50-12-498%
Mephenytoin(CAS 50-12-4) is a hydantoin, used as an anticonvulsant.Mephenytoin(CAS 50
703301MT-DADMe-ImmA653592-04-298% by HNMR/HPLC 
Methylthio-DADMe-immucillin-A (MT-DADMe-ImmA) is an 86-pm inhibitor of human 5-methyl
17031006MI-4631628317-18-998% 
MI-463 is a potent inhibitor of Menin-MLL interaction with an IC50 value of 15.3 nM
17030910ML-098878978-76-898% 
ML-098, also known as CID-7345532, is an activator of the GTP-binding protein Rab7 (E
17030804ML-2651221186-53-398% 
ML265 is a potent PKM2 activator induces tetramerization and reduces tumor formation
17030717MN-6492831-11-398% 
MN-64 is a potent and selective inhibitor of Tankyrase 1 and 2 (IC50 = 6 and 72 nM, r
17030714ML2411346528-06-098% 
ML241 is a potent and selective inhibitors of p97 ATPase. ML241 inhibit p97 ATPase wi
17030712ML348899713-86-198% 
ML348, also known as CID 3238952; SID 160654487, is a reversible LYPLA1 inhibitor wit
17030611MMAF (Monomethyl auristatin F)745017-94-198% 
Monomethyl auristatin F (MMAF) is a synthetic antineoplastic agent. It is part of som
17030308Merimepodib198821-22-698% 
Merimepodib, also known as VX-497, is orally bioavailable IMPDH inhibitor, which inhi