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Other Targets

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Cat. No. Product Name Field of Application Chemical Structure
DC9693 Madrasin Featured Madrasin inhibits pre-mRNA splicing in vitro and modify splicing of endogenous pre-mRNA.
DC8125 ETH 4030(Magnesium ionophore III) Featured Magnesium ionophore III is an onophore used in solvent polymeric membrane electrodes for the assay of Mg2+ activities in blood serum in vitro.
DC11215 MAI-150 MAI-150 is a peptidomimetic inhibitor of APC-Asef interaction, blocks colorectal cancer migration..
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.
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.
DC12536 Malic Enzyme inhibitor ME1 Featured Malic Enzyme inhibitor ME1 (ME1) is a small molecule inhibitor of Malic Enzyme (ME1) with IC50 of 0.15 uM, suppresses growth of human CRC cells in vitro, with little effect on normal rat intestinal epithelial cells..
DCAPI1277 Malotilate Malotilate
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.
DC12138 Maltohexaose (Amylohexaose) Maltohexaose is a natural saccharide, and can be produced from amylose, amylopectin and whole starch.
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.
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.
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.
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..
DC21857 Mapracorat Mapracorat (ZK 245186) is a potent, selective and non-steroid glucocorticoid receptor (GR) agonist with binding Ki of 1.9 nM.
DC4217 Maraviroc Featured Maraviroc (Selzentry, UK-427857, Celsentri) is a CCR5 antagonist for MIP-1α, MIP-1β and RANTES with IC50 of 3.3 nM, 7.2 nM and 5.2 nM, respectively.
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.
DC8909 Maribavir Featured Maribavir(GW257406X; BW1263W94; 1263W94) inhibits HCMV replication is by inhibition of an HCMV encoded protein kinase enzyme called UL97 or pUL97.
DC10639 Marinopyrrole A (Maritoclax) Marinopyrrole A (Maritoclax) is a selective Mcl-1 antagonist. It binds to Mcl-1, but not Bcl-XL, and targets Mcl-1 for proteasomal degradation. Maritoclax disrupts the interaction between Bim and Mcl-1 with an IC50 of 10.1 μM.
DC22297 Marmesin Featured Marmesin is a coumarin originally isolated from the mature bark of A. marmelos.
DC20883 Maropitant citrate Maropitant citrate (Cerenia) is a selective neurokinin 1 receptor (NK1) antagonist for prevention of vomiting due to motion sickness in dogs..
DC20443 MARPIN MARPIN is a novel ATR-Chk1 pathway inhibitor that inhibits hydroxyurea (HU)-induced phosphorylation of Ser345 on Chk1 with IC50 of 7.7 uM.
DC10062 MBP146-78 Featured MBP146-78 inhibits the growth of Eimeria spp. both in vitro and in vivo.
DC12094 MBQ-167 MBQ-167 is a dual Rac/Cdc42 inhibitor, with IC50s of 103 nM for Rac 1/2/3 and 78 nM for Cdc42 in MDA-MB-231 cells, respectively.
DC7193 MBX-2982 Featured MBX-2982 is a selective, orally-available GPR119 agonist for the treatment of type 2 tiabetes.
DC10872 MBX-4132 Featured MBX-4132 a trans translation inhibitor by binding to the bacterial ribosome.
DC21270 MC-1575 MC-1575 is a potent and selective class IIa HDAC inhibitor with IC50 of 440 nM for maize HD1-A, displays >70-fold selectivity over HD1-B.
DC12527 MC180295 Featured MC180295 (MC-180295, MC 180295) is a novel potent, highly selective CDK9 inhibitor with IC50 of 5 nM, displays >22-fold selectivity over other CDKs.
DC23370 MC2884 MC2884 is a novel hybrid, dual HAT/EZH2 inhibitor with IC50 of 3.27, 8.35 and 4.56 uM for CBP, KAT5 and p300, respectively.
DC11358 CPP32 Fluorogenic Substrate III Mca-DEVDAPK(Dnp)-OH is a substrate for caspase-3.

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