| Cat.No. | Name | Information |
|---|---|---|
| M6098 | Baicalein | Baicalein is a CYP2C9 and prolyl endopeptidase inhibitor, IC50 value of 3.12 mM. |
| M9325 | EGTA | EGTA is a specific calcium chelator with a Kd of 60.5 nM at physiological pH (7.4) and a high specificity for Ca2+ than for Mg2+.EGTA significantly inhibits the substrate adhesion capacity of inflammatory macrophages. |
| M9330 | Brij-35 | Brij-35 (Polidocanol) is a high HLB, ethoxylated, nonionic ether of lauryl alcohol with broad pH stability. |
| M6154 | 2-PMPA tetrasodium | 2-PMPA (PMPA tetrasodium salt) is a potent and selective inhibitor of glutamate carboxypeptidase II (GCPII) with an IC50 of 300 pM. |
| M2250 | Pamidronate disodium | Pamidronate disodium is a nitrogen containing bisphosphonate, used to the research of preventing osteoporosis. |
| M9916 | DPPH | DPPH (2,2-Diphenyl-1-picrylhydrazyl) is a stable free radical that measures the free radical scavenging activity of antioxidants. |
| M9194 | Insulin (human) | Insulin (human) is a polypeptide hormone that regulates the level of sugar (glucose) in the blood and is produced by beta cells of islets. |
| M3409 | Formestane | Formestane is a second generation selective aromatase inhibitor with an IC50 of 80 nM. |
| M9665 | N-(2-amino-2-oxoethyl)acrylamide | N-(2-Amino-2-oxoethyl)acrylamide |
| M7791 | Exo-1 | Exo1 is a reversible inhibitor of exocytosis, also a Golgi ARF 1 (ADP-Ribosylation Factor) GTPase activator. |
| M8123 | Quinidine sulfate salt dihydrate | Class IA antiarrhythmic; potassium channel blocker. |
| M8122 | PF-06456384 trihydrochloride | PF-06456384 is a highly potent and selective inhibitor against voltage-gated sodium channel NaV1. |
| M8103 | CP724714 | CP724714 is a potent and selective inhibitor of HER2/ErbB2 with an IC50 value of 10 nM. |
| M8042 | CP-335963 | CP-335963 is an aurora 2 kinase inhibitor, PDGF inhibitor, and anti-proliferative. |
| M8034 | Dofetilide | Dofetilide is a Class III antiarrhythmic and hERG channel blocker. |
| M8000 | Pirenperone | 5-HT2 serotonin receptor antagonist. |
| M7996 | PRL-3 Inhibitor I | PRL-3 Inhibitor I is a rhodanine derivative with an IC50 value of 0. |
| M7988 | 5Z-7-Oxozeaenol | 5Z-7-oxozeaenol is a potent ATP-competitive irreversible inhibitor of ERK2 (IC50 = 80 nM), TAK1 (MEKK7), MKK7, and MEK1, which all contain a common cysteine residue in the ATP-binding site. |
| M7983 | 9,12-Octadecadiynoic acid | Potent cyclooxygenase and lipoxygenase inhibitor. |
| M7969 | NS3694 | NS3694 is an Inhibitor of apoptosome formation. |
| M7966 | Norharmane | Inhibitor of indoleamine 2,3-dioxygenase (IDO). |
| M7953 | NKY80 | NKY80 is a selective adenylyl cyclase-V inhibitor with greater than 200-fold selectivity for type V over the type II isoform. |
| M7950 | NO-1886 | Lipoprotein lipase activator. |
| M7949 | Nisoxetine hydrochloride | Nisoxetine hydrochloride is a potent, selective norepinephrine transporter inhibitor (Ki = 5.1 nM). |
| M7945 | Pimonidazole | Pimonidazole is an effective and nontoxic exogenous 2-nitroimidazole hypoxia marker. Pimonidazole accumulates in hypoxic cells via covalent binding with macromolecules or by forming reductive metabolites after reduction of its nitro group, it can be used for qualitative and quantitative assessment of tumor hypoxia. |
| M7899 | L-655,708 | Novel ligand selective for the benzodiazepine site of GABAA receptors which contain the α5 subunit. |
| M7887 | α-Linolenic acid | An ω-3 fatty acid that serves as a precursor to eicosapentaenoic acid (EPA) but not docosahexaenoic acid. |
| M7884 | Lidocaine N-ethyl chloride | Lidocaine N-ethyl chloride is an intracellular voltage-gated sodium channel blocker. |
| M7873 | Kynurenic acid | Kynurenic acid is a non-selective antagonist at NMDA and AMPA/kainate receptors; blocks kainic acid neurotoxicity. |
| M7867 | JNJ-10198409 | JNJ-10198409 is a potent ATP-competitive inhibitor of Platelet-Derived Growth Factor receptor tyrosine kinase (PDGF-RTK) with both antiangiogenic and a direct tumor cell antiproliferative activity. |
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