yingweiwo

New1

New1

New1 related products

Structure Cat No. Product Name CAS No. Product Description
m-PEG9-phosphonic acid V25951 m-PEG9-phosphonic acid 2055016-25-4 m-PEG9-phosphonic acid is a PROTAC (PROteolysis TArgeting Chimera) linker of the Polyethylene glycol (PEG) category.
m-PEG9-Tos V25952 m-PEG9-Tos 82217-01-4 Tos-PEG8-m is an analogue of silybin ether, disclosed in patent CN105037337A (compound III-d).
M-乙基苯磺酰氟 V12449 Benzenesulfonyl fluoride, 3-ethyl- 34586-50-0 Benzenesulfonyl fluoride, 3-ethyl- is a novel and potent bioactive compound
M-二甲氨基苯基脲 V25140 M-dimethylaminophenyl urea 26455-21-0 M-dimethylaminophenyl urea is a novel and potent bioactive compound
M-双(m-苯氧基苯氧基)苯 V6460 1,3-Bis(3-phenoxyphenoxy)benzene 2455-71-2 1,3-Bis(3-phenoxyphenoxy)benzene is a novel and potent bioactive compound
M1000907 V12861 M1000907 880759-45-5 M1000907 is a novel and potent 5-HT2A receptor antagonist
M1001 V14813 M1001 874590-32-6 M1001 is a weak hypoxia-inducible factor-2α (HIF-2α) agonist.
M122 V24864 M122 2127411-50-9 M122 is a novel and potent histone deacetylase HDAC1 and HDAC2 inhibitor and antitumor agent
M133 V24865 M133 2127411-61-2 M133 is a novel and potent histone deacetylase HDAC1 and HDAC2 inhibitor and antitumor agent
M199 V19447 M199 1051933-86-8 M199 is a novel and potent inhibitor of TLR3/9 which can induce the secretion of IL-6, IL-8 and TNFalpha in human PBMCs.
M2698 HCl V24867 M2698 HCl 1379545-95-5 M2698 (M-2698, MSC2363318A) HCl, the hydrochloride salt ofM2698, is a novel, oral and ATP competitive dual inhibitor of the serine/threonine protein kinases ribosomal protein S6 Kinase (p70S6K) and Akt (protein kinase B) withanticancer activity.
M410 V10438 M410 M410 is a novel and potent vascular disrupting agent
M443 V24873 M443 1820684-31-8 M443 is an irreversible and specific inhibitor of MRK with IC50 of <125 nM.
M6407 V24877 M6407 5201-88-7 M6407 is a novel and potent bioactive compound
M7594_0037 V24878 M7594_0037 774551-07-4 M7594_0037 is a novel and potent inhibitor of human peptide deformylase (HsPDF)
M77976 V24879 M77976 394237-61-7 M77976 is a specific, ATP-competitive inhibitor of pyruvate dehydrogenase kinase PDK4 with IC50 of 648 μM.
MA-2029 V24881 MA-2029 287206-61-5 MA-2029 is a selective, orally bioactive and competitive motilin receptor blocker (antagonist) (IC50=4.9 nM).
MA242 TFA V24882 MA242 TFA 1049704-18-8 MA242 is a specific dual (bifunctional) inhibitor of MDM2 and NFAT1.
MAC-0547630 V24886 MAC-0547630 950386-41-1 MAC-0547630 is a novel and potent inhibitor of UppS
MAC13243 HCl V24887 MAC13243 HCl 1071638-38-4 MAC13243 is an anti-bacterial agent and an inhibitor (blocker/antagonist) of the bacterial lipoprotein targeting chaperone LolA.
Contact Us