Free shipping on all orders over $ 500
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). |
Products are for research use only. Not for human use. We do not sell to patients.
© Copyright 2010-2017 AbMole BioScience. All Rights Reserved.
