Cat. No. | Product name | CAS No. |
DC22728 |
M-110
M-110 is a potent, selective inhibitor of PIM kinase family with preference for PIM-3 with IC50 of 0.047, 2.5 and 2.5 uM for PIM3, PIM1 and PIM2, respectively. |
1395048-49-3 |
DC21264 |
M4284
M4284 (M-4284) is a high-affinity biphenyl mannoside FimH inhibitor with HAI of 16 nM in hemagglutination assay. |
1373346-85-0 |
DC21265 |
M-525
M-525 is a first-in-class, highly potent, irreversible small-molecule inhibitor of the menin-MLL interaction with binding IC50 of 3.3 nM in FP assays. |
2173582-08-4 |
DC21339 |
MAC1
MAC1 (Monastrol Antagonizing Compound 1) is a small molecule that can rescue spindle bipolarity in cells lacking Eg5 activity. |
325970-42-1 |
DC21266 |
MAC13772
MAC13772 is a potent inhibitor of BioA with an IC50 of 250 nM, a novel antibacterial inhibitor that selectively inhibits PABA biosynthesis in M tuberculosis.. |
4871-40-3 |
DC21267 |
MAC168425
MAC168425 is a novel antibacterial inhibitor that interferes with glycine metabolism in E coli.. |
2138-33-2 |
DC21268 |
MAC173979
MAC173979 is a novel time-dependent inhibitor of p-aminobenzoic acid biosynthesis with IC50 of 30 uM, represents the first PABA biosynthesis inhibitor with activity against Gram-negative bacteria.. |
41501-64-8 |
DC9922 |
Macranthoidin B
Macranthoidin B is a major bioactive saponin in rat plasma after oral administration of extraction of saponins from Flos Lonicerae. |
136849-88-2 |
DC11215 |
MAI-150
MAI-150 is a peptidomimetic inhibitor of APC-Asef interaction, blocks colorectal cancer migration.. |
2143041-32-9 |
DC11201 |
MAI-400
MAI-400 (MAI400) is a novel peptide inhibitor of APC-Asef interaction with Kd of 12 nM and IC50 of 0.25 uM. |
|
DC23792 |
MAL3-101
MAL3-101 is a Hsc70 modulator that inhibits Hsp70 ATPase activity, exhibits antiproliferative activity in breast cancer cells SK-BR-3 with IC50 of 27 uM. |
912361-26-3 |
DC22143 |
MALAT1-IN-1
Featured
MALAT1 inhibitor 5 (Malat1 inhibitor 5) is a selective small molecule targeting of Metastasis-associated lung adenocarcinoma transcript 1 (Malat1/MALAT1 mouse/human), a highly conserved long non-coding RNA; does not affect Neat1 lncRNA levels. |
827327-28-6 |
DC11066 |
MALT1 paracaspase inhibitor 3
MALT1 paracaspase inhibitor 3 is a potent, specific, covalent inhibitor of MALT1 paracaspase with Ki of 10 nM, exhibits 10-and 100-fold improved potency in vitro and in vivo compared with Z-VRPR-fmk. |
2088355-90-0 |
DC20141 |
Maltitol
Featured
Maltitol is a sugar alcohol used as a sugar substitute. It has 75-90% of the sweetness of sucrose (table sugar) and nearly identical properties. Maltitol may also be used as a plasticizer in gelatin capsules, as an emollient, and as a humectant. |
585-88-6 |
DC12138 |
Maltohexaose (Amylohexaose)
Maltohexaose is a natural saccharide, and can be produced from amylose, amylopectin and whole starch. |
34620-77-4 |
DC12157 |
Maltopentaose (Maltopentose)
Maltopentaose is the shortest chain oligosaccharide that can be classified as maltodextrin and is also used in a study to investigate glycation and phosphorylation of α-lactalbumin. |
34620-76-3 |
DC11315 |
Manidipine(CV-4093)
Manidipine is a dihydropyridine L- and T-type calcium channel blocker. |
89226-50-6 |
DC23814 |
MAP4K4-IN-17
Featured
MAP4K4-IN-17 is a potent and highly selective MAP4K4 inhibitor with IC50 of 14.9 nM, showes improved overall drug-like properties compared to PF-06260933. |
1811510-58-3 |
DC21916 |
MAP4K4-IN-37
MAP4K4-IN-37 is a potent, selective, orally active inhibitor of serine-threonine kinase MAP4K4 with IC50 of 0.4 nM. |
2089334-01-8 |
DC20442 |
MAP4K4-IN-44
MAP4K4-IN-44 is a potent, moderately selective small molecule MAP4K4 inhibitor with IC50 of 5 nM in LC3K assay, demonstrates favorable in vivo bioavailability in mouse.. |
1623464-28-7 |
DC21857 |
Mapracorat
Mapracorat (ZK 245186) is a potent, selective and non-steroid glucocorticoid receptor (GR) agonist with binding Ki of 1.9 nM. |
887375-26-0 |
DC21269 |
Marbostat-100
Marbostat-100 is a potent, selective HDAC6 inhibitor with Ki of 0.7 nM, displays >200-fold selectivity over HDAC1-5, and HDAC7-10. |
1876450-69-9 |