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Products

Catalog NoChemical NameCAS NumberPurityChemical Structure
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
17030612Mavoglurant543906-09-898% 
Mavoglurant, aslo known as AFQ056, is an experimental drug candidate for the treatmen
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
17030302ML-2641550008-55-398% 
ML-264 is a Krppel-like factor 5 (KLF5) inhibitor That Potently Inhibits Growth of Co
17030109MK-82451030612-90-898% 
MK-8245 is a potent, liver-targeted SCD inhibitor with preclinical antidiabetic and a
17030101MLN-11171268454-23-498% 
Serabelisib (also known as MLN1117, INK1117, and TAK-117) is an orally bioavailable i
17022811ML-2811404437-62-298% 
ML-281 is a potent ans selective STK33 inhibitor (IC50 = 14 nM). ML281 showed low nan
17022804Maraviroc376348-65-198% 
Maraviroc (UK-427857; Selzentry; Celsentri) is a selective CCR5 antagonist (IC50= 6.4
17022403MMAE (Monomethyl auristatin E)474645-27-798% 
MMAE, also known as Monomethyl auristatin E, is a synthetic antineoplastic agent. Bec
17021322Monastrol329689-23-898% 
Monastrol is a cell-permeable small molecule inhibitor of kinesin-5(KIF11) which is
17021313MS0491502816-23-098% 
MS049 is a potent and selective inhibitor of PRMT4 and PRMT6 with IC50s of 34 nM
17021301Miransertib(ARQ 092)1313883-00-998% 
ARQ 092 is a novel, orally bioavailable and selective AKT pathway inhibitor exhibit
712101MT-DADMe-ImmA(MTDIA HCl)1399840-35-798% 
Methylthio-DADMe-immucillin-A (MT-DADMe-ImmA) is an 86-pm inhibitor of human 5-methyl
170119087-Methyl-7H-pyrrolo[2,3-d]pyriMidin-4-aMine7752-54-798% 
7-Methyl-7H-pyrrolo[2,3-d]pyriMidin-4-aMine 
17011107ML-7110448-33-498% 
ML-7 is an inhibitor of smooth muscle myosin light chain kinase (MLCK) with a Ki 
17011105MX691005264-47-098% 
MX69 is a MDM2/XIAP inhibitor, used for cancer treatment.