Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
16123055 | MK-571 sodium salt | 115104-28-4 | 98% | |
MK-571 is a selective, orally active CysLT1 receptor antagonist. It blocks the bindin | ||||
16123053 | Mizoribine | 50924-49-7 | 98% | |
Mizoribine,Mizoribine (INN, trade name Bredinin) is an immunosuppressive drug. The co | ||||
16123052 | Mivebresib | 1445993-26-9 | 98% | |
Mivebresib, also known as ABBV-075, is a potent BET inhibitor (bromodomain (BRD)-cont | ||||
16123051 | Mitoxantrone HCl | 65271-80-9 | 98% | |
Mitoxantrone hydrochloride is the hydrochloride salt of an anthracenedione antibiotic | ||||
16123049 | Mirin | 1198097-97-0 | 98% | |
Mirin is a Mre11-Rad50-Nbs1 (MRN)-ATM pathway inhibitor. | ||||
16123048 | Migalastat HCl | 75172-81-5 | 98% | |
Migalastat HCl, also known as AT1001 or GR181413A, is a pharmacological chaperone tha | ||||
16123047 | MI-2 (MALT1 inhibitor) | 1047953-91-2 | 98% | |
MI-2 is a MALT1 inhibitor (IC50 = 5.84 M). MI-2 binds directly to MALT1 and irreversi | ||||
16123046 | MG-101 | 110044-82-1 | 98% | |
MG-101, also known as Calpain Inhibitor I and ALLN, is a calpain inhibitor (IC50 = 0. | ||||
16123045 | Mertansine (DM1) | 139504-50-0 | 98% | |
Mertansine refers to the thiol-containing maytansinoid, DM1 (N2-deacetyl-N2-(3-mercap | ||||
16123044 | Medroxyprogesterone Acetate | 71-58-9 | 98% | |
Medroxyprogesterone Acetate, also known as MPA, is a steroidal progestin, a synthetic | ||||
16122832 | MC-976 | 129831-99-8 | 98% | |
MC-976 is an Vitamin D3 derivative. | ||||
16122831 | Mafodotin | 863971-19-1 | 98% | |
Mafodotin, also known as mc-MMAF and SGD-1269 or Maleimidocaproyl monomethylauristati | ||||
16122830 | Madrasin | 374913-63-0 | 98% | |
Madrasin is a potent and cell penetrant splicing inhibitor that interferes with the e | ||||
16122829 | M2I-1 | 312271-03-7 | 98% | |
M2I-1, also known as Mad2 Inhibitor-1, is Protein-Protein Interaction Inhibitor Targe | ||||
161227105 | MK571 | 115103-85-0 | 98% | |
MK-571 is a selective, orally active CysLT1 receptor(Cysteinyl leukotriene receptor) | ||||
16122796 | MPTP hydrochloride | 23007-85-4 | 98% | |
MPTP hydrochloride is a dopaminergic neurotoxin and cause selective destruction of do | ||||
16122790 | ML323 | 1572414-83-5 | 98% | |
ML323 is a highly potent and selective USP1-UAF1 inhibitor with IC50 of 76 nM.ML323 i | ||||
16122749 | ML390 | 98% | ||
ML390 is a human DHODH inhibitor that induces differentiation in acute myeloid leukem | ||||
16122745 | MRT67307 | 1190378-57-4 | 98% | |
MRT67307 is a potent and dual IKKϵ and TBK1 inhibitor with IC50 of 160 and 19 nM, re | ||||
16122717 | MK-4827(Niraparib) tosylate | 1038915-73-9 | 98% | |
MK-4827(Niraparib) tosylate is a selective inhibitor of PARP1/PARP2 with IC50 of 3.8 | ||||
6111524 | MP-A08 | 219832-49-2 | 98% | |
MP-A08 is a highly selective ATP competitive SK inhibitor that targets both SK1 and S | ||||
6111404 | Mcl1-IN-2 | 292057-76-2 | 98% | |
Mcl1-IN-2 is a Mcl-1 inhibitor without reported IC50 value. | ||||
6111403 | Marinopyrrole A | 1227962-62-0 | 98% | |
Marinopyrrole (Maritoclax) is a novel and specific Mcl-1 inhibitor with an IC50 value | ||||
61116 | ML224 | 1338824-21-7 | 98% | |
ML224(NCGC00242364; ANTAG3) is a selective TSHR inverse agonist; inhibits TSH-stimula | ||||
61114 | (±)-Methotrimeprazine D6 | 1189805-51-3 | 98% | |
()-Methotrimeprazine (D6) is the deuterium labeled Methotrimeprazine, which is a D3 d | ||||
6111017 | Motolimod | 926927-61-9 | 98% | |
Motolimod | ||||
6111014 | MCC950 sodium | 256373-96-3 | 98% | |
MCC950 (CP 456773) sodium is a potent, selective, small molecule inhibitor of NLRP3 w | ||||
6111012 | MS023 | 1831110-54-3 | 98% | |
MS023 is a potent, selective, and cell-active inhibitor of human type I PRMTs with IC | ||||
6111008 | MK-4101 | 935273-79-3 | 98% | |
MK-4101 is a potent SMO Inhibitor of the Hedgehog PathwayMK-4101 is a potent SMO Inhi | ||||
611940 | ML346 | 100872-83-1 | 98% | |
ML346 is a novel activator of Hsp70 with EC50 of 4600 nM in HeLa cell toxicity assay. |
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