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Abmole Inhibitor Catalog 2017

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Inhibitors

Cat.No.  Name Information
M8905 EBE-A22 EBE-A22 is a derivative of PD 153035, has no effect on EGF-R TK but maintains a high cytotoxic profile.
M8904 NIH-12848 NIH-12848 is a putative phosphatidylinositol 5-phosphate 4-kinase γ (PI5P4Kγ) inhibitor.
M8901 CHS-828 CHS-828 (GMX1778) is a potent and specific inhibitor of NAMPT with IC50 and Kd value of <25 nM and 120 nM, respectively.
M8898 APY0201 APY0201 is a potent and selective IL-12/23 inhibitor.
M8896 MDK36122 MDK36122, also known as H-PGDS Inhibitor I, is a Prostaglandin D Synthase (hematopoietic-type) Inhibitor with an IC50 Value of 0.7 nM.
M8894 GJ-103 GJ-103 is an active analog of the read-through compound GJ072.
M8893 Miriplatin Miriplatin is a chemotherapy agent which belongs to the class of alkylating agents.
M8892 Coluracetam Coluracetam (MKC-231) is a new choline uptake enhancer.
M8891 AI-1 AI-1 is a negative regulator of Nrf2.
M8890 Forchlorfenuron Forchlorfenuron is a synthetic cytokinin that inhibits septins and exhibits anti-parasitic, anticancer, and anti-angiogenic activities.
M8889 6-Methoxy-2-naphthoic acid 6-Methoxy-2-naphthoic acid is an NMDA receptor modulator.
M8883 Ceforanide Ceforanide is a new cephalosporin with antibacterial activity and has a longer elimination half-life than any currently available cephalosporin.
M8878 Inositol Nicotinate Inositol Nicotinate is a formulation of niacin, which is also called vitamin B3, an essential human nutrient.
M8875 ND-630 ND-630 is an ACC inhibitor of human ACC1 and ACC2 with IC50 values of 2.1 and 6.1 nM, respectively.
M8873 D-Luciferin potassium salt D-Luciferin potassium salt is the substrate of luciferases that catalyze the production of light in bioluminescent insects.
M8872 ZD 7114 hydrochloride ZD 7114 is a selective β3 adrenergic receptor agonist.
M8870 Zopolrestat Zopolrestat is an inhibitor of Aldose Reductase.
M8869 Zinterol hydrochloride Zinterol Hydrochloride is a β2 adrenergic receptor selective agonist.
M8868 Zerumbone Zerumbone is a TRAIL-induced apoptosis potentiator.
M8867 Zaragozic acid A trisodium salt Potent inhibitor, in vivo and in vitro, of mammalian, fungal and Saccharomyces cervisiae squalene synthase.
M8866 Zonisamide sodium salt Zonisamide sodium salt is an anti-epileptic.
M8865 Zimelidine dihydrochloride Serotonin transport blocker; antidepressant.
M8864 Zotepine Zotepine is an atypical antipsychotic.
M8863 YM 976 Phosphodiesterase type IV (PDE4) inhibitor.
M8862 YH439 YH439 is an aryl hydrocarbon receptor activator.
M8861 Xaliproden hydrochloride 5-HT1A serotonin receptor agonist; neuroprotectant.
M8860 X80 X80 is an inhibitor of xeroderma pigmentosum group A protein (XPA protein) required for the removal of all types of DNA lesions repaired by nucleotide excision repair Including both transcription coupled and global genomic nucleotide excision repair.
M8859 Xestospongin C Xestospongin C is a selective, reversible and membrane-permeable inhibitor of IP3 receptor.
M8858 XE-991 XE-991 is a KCNQ channel blocker; which is more potent than linopiridine.
M8857 Xylazine α2-adrenoceptor agonist, sedative, muscle relaxant.
M8855 WR99210 WR99210 is a potent inhibitor of Plasmodium falciparum dihydrofolate reductase (DHFR), which is a major malarial drug target.
M8854 WAY-100635 maleate salt WAY-100635 maleate salt is a highly selective 5-HT1A serotonin receptor antagonist.
M8853 WIN 62,577 Non-peptide NK1 tachykinin receptor antagonist.
M8852 W-84 dibromide Potent allosteric modulator of M2 muscarinic acetylcholine receptors.
M8851 WAY 161503 hydrochloride The 5-HT2C receptors have been implicated in conditions including obesity, anxiety, depression, OCD, schizophrenia, migraine, nociception and erectile dysfunction.
M8850 WAY-213613 WAY-213613 is a selective GLT-1/EAAT2 inhibitor.
M8849 VO-OHpic trihydrate VO-OHpic trihydrate is a PTEN (phosphatase and tensin homologue deleted on chromosome 10) inhibitor.
M8848 VU0152100 Positive allosteric modulator of muscarinic choline receptor M4.
M8847 Valnoctamide Valproic acid (VPA) and derivatives such as valpromide and valnoctamide are anti-convulsant, mood stabilizing drugs, believed to function as indirect GABA agonists by inhibiting the transamination of GABA.
M8846 VU0238429 VU0238429 is a selective muscarinic acetylcholine receptor 5 (M5) positive allosteric modulator; causes leftward shift in acetylcholine potency.
M8845 Valpromide Valpromide (VPD) is a derivative of valproic acid (VPA) and is used as an antiepileptic drug.
M8844 Valeryl Salicylate Selective, irreversible COX-1 inhibitor.
M8843 Verrucarol Trichothecene mycotoxin that is a component of toxic mold.
M8842 Valinomycin K+-selective ionophoric cyclodepsipeptide; potassium ionophore which uncouples oxidative phosphorylation, induces apoptosis in murine thymocytes, inhibits NGF-induced neuronal differentiation and antagonizes ET-induced vasoconstriction.
M8841 Carboxytolbutamide In vivo tolbutamide metabolite.
M8840 Oxidized Nifedipine CYP3A4 nifedipine metabolite.
M8839 U-74389G Free radical lipid peroxidation inhibitor in cultured brain cells, monocytic THP1 cells, and LLC-PK1 cell layers.
M8838 UBP302 UBP302 is a selective GluR5 antagonist.
M8837 UK-78282 monohydrochloride UK-78282 blocks both Kv1.
M8836 U 18666A Inhibitor of cholesterol synthesis (inhibits desmosterol Δ24-reductase).


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