Structure | Cat No. | Product Name | CAS No. | Product Description |
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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. |
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V25952 | m-PEG9-Tos | 82217-01-4 | Tos-PEG8-m is an analogue of silybin ether, disclosed in patent CN105037337A (compound III-d). |
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V12449 | Benzenesulfonyl fluoride, 3-ethyl- | 34586-50-0 | Benzenesulfonyl fluoride, 3-ethyl- is a novel and potent bioactive compound |
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V25140 | M-dimethylaminophenyl urea | 26455-21-0 | M-dimethylaminophenyl urea is a novel and potent bioactive compound |
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V6460 | 1,3-Bis(3-phenoxyphenoxy)benzene | 2455-71-2 | 1,3-Bis(3-phenoxyphenoxy)benzene is a novel and potent bioactive compound |
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V12861 | M1000907 | 880759-45-5 | M1000907 is a novel and potent 5-HT2A receptor antagonist |
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V14813 | M1001 | 874590-32-6 | M1001 is a weak hypoxia-inducible factor-2α (HIF-2α) agonist. |
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V24864 | M122 | 2127411-50-9 | M122 is a novel and potent histone deacetylase HDAC1 and HDAC2 inhibitor and antitumor agent |
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V24865 | M133 | 2127411-61-2 | M133 is a novel and potent histone deacetylase HDAC1 and HDAC2 inhibitor and antitumor agent |
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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. |
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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. |
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V10438 | M410 | M410 is a novel and potent vascular disrupting agent | |
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V24873 | M443 | 1820684-31-8 | M443 is an irreversible and specific inhibitor of MRK with IC50 of <125 nM. |
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V24877 | M6407 | 5201-88-7 | M6407 is a novel and potent bioactive compound |
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V24878 | M7594_0037 | 774551-07-4 | M7594_0037 is a novel and potent inhibitor of human peptide deformylase (HsPDF) |
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V24879 | M77976 | 394237-61-7 | M77976 is a specific, ATP-competitive inhibitor of pyruvate dehydrogenase kinase PDK4 with IC50 of 648 μM. |
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V24881 | MA-2029 | 287206-61-5 | MA-2029 is a selective, orally bioactive and competitive motilin receptor blocker (antagonist) (IC50=4.9 nM). |
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V24882 | MA242 TFA | 1049704-18-8 | MA242 is a specific dual (bifunctional) inhibitor of MDM2 and NFAT1. |
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V24886 | MAC-0547630 | 950386-41-1 | MAC-0547630 is a novel and potent inhibitor of UppS |
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V24887 | MAC13243 HCl | 1071638-38-4 | MAC13243 is an anti-bacterial agent and an inhibitor (blocker/antagonist) of the bacterial lipoprotein targeting chaperone LolA. |