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Products

Catalog NoChemical NameCAS NumberPurityChemical Structure
16123055MK-571 sodium salt115104-28-498% 
MK-571 is a selective, orally active CysLT1 receptor antagonist. It blocks the bindin
16123053Mizoribine50924-49-798% 
Mizoribine,Mizoribine (INN, trade name Bredinin) is an immunosuppressive drug. The co
16123052Mivebresib1445993-26-998% 
Mivebresib, also known as ABBV-075, is a potent BET inhibitor (bromodomain (BRD)-cont
16123051Mitoxantrone HCl65271-80-998% 
Mitoxantrone hydrochloride is the hydrochloride salt of an anthracenedione antibiotic
16123049Mirin1198097-97-098% 
Mirin is a Mre11-Rad50-Nbs1 (MRN)-ATM pathway inhibitor.
16123048Migalastat HCl75172-81-598% 
Migalastat HCl, also known as AT1001 or GR181413A, is a pharmacological chaperone tha
16123047MI-2 (MALT1 inhibitor)1047953-91-298% 
MI-2 is a MALT1 inhibitor (IC50 = 5.84 M). MI-2 binds directly to MALT1 and irreversi
16123046MG-101110044-82-198% 
MG-101, also known as Calpain Inhibitor I and ALLN, is a calpain inhibitor (IC50 = 0.
16123045Mertansine (DM1)139504-50-098% 
Mertansine refers to the thiol-containing maytansinoid, DM1 (N2-deacetyl-N2-(3-mercap
16123044Medroxyprogesterone Acetate71-58-998%
Medroxyprogesterone Acetate, also known as MPA, is a steroidal progestin, a synthetic
16122832MC-976129831-99-898% 
MC-976 is an Vitamin D3 derivative.
16122831Mafodotin863971-19-198% 
Mafodotin, also known as mc-MMAF and SGD-1269 or Maleimidocaproyl monomethylauristati
16122830Madrasin374913-63-098% 
Madrasin is a potent and cell penetrant splicing inhibitor that interferes with the e
16122829M2I-1312271-03-798% 
M2I-1, also known as Mad2 Inhibitor-1, is Protein-Protein Interaction Inhibitor Targe
161227105MK571115103-85-098% 
MK-571 is a selective, orally active CysLT1 receptor(Cysteinyl leukotriene receptor)
16122796MPTP hydrochloride23007-85-498% 
MPTP hydrochloride is a dopaminergic neurotoxin and cause selective destruction of do
16122790ML3231572414-83-598% 
ML323 is a highly potent and selective USP1-UAF1 inhibitor with IC50 of 76 nM.ML323 i
16122749ML39098% 
ML390 is a human DHODH inhibitor that induces differentiation in acute myeloid leukem
16122745MRT673071190378-57-498% 
MRT67307 is a potent and dual IKKϵ and TBK1 inhibitor with IC50 of 160 and 19 nM, re
16122717MK-4827(Niraparib) tosylate1038915-73-998% 
MK-4827(Niraparib) tosylate is a selective inhibitor of PARP1/PARP2 with IC50 of 3.8
6111524MP-A08219832-49-298% 
MP-A08 is a highly selective ATP competitive SK inhibitor that targets both SK1 and S
6111404Mcl1-IN-2292057-76-298% 
Mcl1-IN-2 is a Mcl-1 inhibitor without reported IC50 value.
6111403Marinopyrrole A1227962-62-098% 
Marinopyrrole (Maritoclax) is a novel and specific Mcl-1 inhibitor with an IC50 value
61116ML2241338824-21-798% 
ML224(NCGC00242364; ANTAG3) is a selective TSHR inverse agonist; inhibits TSH-stimula
61114(±)-Methotrimeprazine D61189805-51-398% 
()-Methotrimeprazine (D6) is the deuterium labeled Methotrimeprazine, which is a D3 d
6111017Motolimod926927-61-998% 
Motolimod
6111014MCC950 sodium256373-96-398% 
MCC950 (CP 456773) sodium is a potent, selective, small molecule inhibitor of NLRP3 w
6111012MS0231831110-54-398% 
MS023 is a potent, selective, and cell-active inhibitor of human type I PRMTs with IC
6111008MK-4101935273-79-398% 
MK-4101 is a potent SMO Inhibitor of the Hedgehog PathwayMK-4101 is a potent SMO Inhi
611940ML346100872-83-198% 
ML346 is a novel activator of Hsp70 with EC50 of 4600 nM in HeLa cell toxicity assay.