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Cat. No. Product Name Field of Application Chemical Structure
DC24209 MDK7229(MD2-IN-1) Featured MDK7229, also known as MD2-IN-1 is a MD2 (Myeloid differentiation protein 2) inhibitor.
DC10570 MDK74978(Multi-kinase inhibitor) Featured MDK74978, also known as Multi-kinase inhibitor I, is a Multi-kinase inhibitor. MDK74978 has CAS#778274-97-8. The last 5 digit was used in its name.
DC12028 MDK7526(Protein degrader 1) Featured MDK7526, also known as VHL Ligand 1; Protein degrader 1, is a potent and selective protein degrader.
DC10571 MDK-8582(Hnps-PLA Inhibitor) Featured MDK-8582, also known as Hnps-PLA Inhibitor, is an nhibitor of human nonpancreatic secretory Phospholipase A (hnps-PLA).
DC7194 MDL 29951 Featured MDL-29951 is a novel glycine antagonist of NMDA receptor activation (Ki=0.14 mM, [3H]glycine binding) in vitro and in vivo.
DC5069 Enzalutamide (MDV3100) Featured MDV3100 is an androgen-receptor (AR) antagonist with IC50 of 36 nM.
DC10650 MDVN1003 Featured MDVN1003 is a potent inhibitor of BTK amd PI3K delta.
DC11141 ME0328 Featured ME0328 is an inhibitor of PARP3 (IC50 = 0.89 µM), which is a regulator of DNA repair and mitotic progression.
DC23739 Meayamycin Meayamycin is an analogue of FR901464 that binds to the splicing factor 3b (SF3b) complex and inhibits pre-mRNA splicing, shows picomolar antiproliferative activity against various cancer cell lines and multidrug-resistant cells..
DC10258 Mebendazole Mebendazole is a synthetic benzimidazole derivate and anthelmintic agent. Mebendazole interferes with the reproduction and survival of helminths by inhibiting the formation of their cytoplasmic microtubules, thereby selectively and irreversibly blocking g
DCAPI1081 Mecarbinate Mecarbinate
DC7757 (R)-Meclizine Meclizine is a histamine H1 receptor antagonist used to treat nausea and motion sickness.
DC9035 Meclofenoxate HCl Meclofenoxate hydrochloride, an ester of dimethylethanolamine (DMAE) and 4-chlorophenoxyacetic acid (pCPA), has been shown to improve memory, have a mentally stimulating effect, and improve general cognition.
DCAPI1580 Medetomidine Medetomidine hydrochloride is a potent and highly selective α2-AR adrenoceptor agonist (Ki values are 1.08 and 1750 nM for α2- and α1-adrenoceptors respectively). Shows greater selectivity over α1-adrenoceptors than clonidine and UK 14,304 (1620-, 220- an
DC20446 Mefuparib hydrochloride(CVL218) Featured Mefuparib(CVL218) hydrochloride is a potent, highly selective, competitive PARP1/2 inhibitor with IC50 of 3.2/1.9 nM, respectively.CVL218 was more potent than Remdesivir in blocking Coronavirus infection of cells and equally as potent as Remdesivir in blocking replication of virus once it has entered the cells.
DC7461 Meisoindigo Featured Meisoindigo(Natura-α; N-Methylisoindigotin; Dian III), a derivative of Indigo naturalis, might induce apoptosis and myeloid differentiation of acute myeloid leukemia (AML).
DC26032 Melagatran Melagatran is a synthetic, small-peptide direct thrombin inhibitor with anticoagulant activity.
DC11083 Dersimelagon Featured Dersimelagon, also known as MT-7117 and WHO 10832, is a novel, orally-administered, small molecule, selective melanocortin-1 receptor (MC1R) agonist that increases skin melanin without sun exposure and is being developed to increase light tolerance in EPP/XLP patients. Dersimelagon significantly boosted sunlight tolerance in patients with erythropoietic protoporphyria in a multicenter, phase 2, randomized trial.
DC11353 MIF-1 Melanocyte-stimulating hormone release-inhibiting factor (MSH-R-IF) is a hypothalamic tripeptide that binds to rat striatum (Kd = 4.69 nM) and has diverse biological activities.
DC8311 Meleagrin Meleagrin is an antibiotic derived from a deep ocean, penicillin-producingP. chrysogenum.
DC21274 Melflufen Melflufen (Melphalan flufenamide, J1) is a novel dipeptide and alkylating prodrug of melphalan, inhibits angiogenesis in vitro and in vivo.
DC21917 MELK inhibitor 17 MELK inhibitor 17 is a potent, selective MELK inhibitor with Ki/IC50 of 0.39/3 nM, >100-fold selectivity over CHK1, CAMKK2, NUAK1 and ERK2.
DC10015 MELK-8a Featured MELK-8a is a novel MELK inhibitor.
DC11465 MELK-T1 Featured MELK-T1 is a potent and selective inhibitor of protein kinase MELK.
DCAPI1316 Meloxicam (Mobic) Meloxicam (Mobic)
DC9050 Melphalan Featured Melphalan(Sarcolysin; L-PAM) is a chemotherapy drug belonging to the class of nitrogen mustard alkylating agents; attaches the alkyl group to the guanine base of DNA.
DC9526 Meptazinol (hydrochloride) Featured Meptazinol Hcl(WY-22811 Hcl) is a unique centrally active opioid analgesic.
DC10407 Mequitazine Mequitazine is a potent, nonsedative and long-acting histamine H1 antagonist.
DC7195 JAK Inhibitor I(Merck 5, Pyridone 6) Featured Merck 5 is a potent and reversible ATP-competitive inhibitor of the JAK kinases (JAK1, JAK2, JAK3, and Tyk2). It also blocks IL2 and IL4 dependent proliferation of CTLL cells and inhibits the phosphorylation of STAT5.
DC22506 Merck60 Featured Merck60 (BRD 6929, Compound-60) is a potent, selective and brain-penetrant inhibitor of HDAC1 and HDAC2 with IC50 of 1 nM and 8 nM respectively.

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