| Cat.No. | Name | Information |
|---|---|---|
| M2206 | TH-302 (Evofosfamide) | TH-302 is a highly potent and selective hypoxia-activated procompound targeting hypoxic regions of solid tumors with IC50 of 19 nM. |
| 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 |
| M7930 | Metrazoline | Potent and selective imidazoline binding site ligand. |
| M7928 | E-4031 | E-4031 selectively blocks hERG K+ channels. |
| M7923 | Myoseverin B | Myoseverin, a new microtubule-binding molecule, acts reversibly on myoblast proliferation without the cytotoxic effects displayed by nonpurine-based microtubule-disrupting molecules, like taxol, vinblastine, nocodazole. |
| M7920 | MMPIP | MMPIP is a potent, selective, allosteric antagonist of metabotropic glutamate receptor 7 (mGluR7). |
| M7919 | MDL 72527 | MDL 72527is an inhibitor of polyamine oxidase (spermine oxidase SMO). |
| M7918 | Mosapride citrate salt dihydrate | 5-HT4 receptor agonist and 5-HT3 receptor antagonist. |
| M7914 | MOCPAC | Selective HDAC1 substrate (over HDAC6, class I over class II). |
| M7913 | Mastoparan 17 | Inactive analog of mastoparan; useful as negative control. |
| M7912 | Mastoparan-7 | G protein activator via Gαi and Gαo stimulation, similar to G protein-coupled receptors; peptide originally isolated from wasp venom. |
| M7909 | MDL-12,330A hydrochloride | Adenylyl cyclase inhibitor. |
| M7907 | MPPG | Group III/II metabotropic glutamate (mGluR) receptor antagonist. |
| M7904 | Methiothepin mesylate salt | Methiothepin mesylate salt is a 5-HT1, 5-HT6, 5-HT7 serotonin receptor antagonist, which blocks serotonin autoreceptors. |
| M7900 | LP44 | LP44 is a high affinity 5-HT7 receptor agonist. |
| M7899 | L-655,708 | Novel ligand selective for the benzodiazepine site of GABAA receptors which contain the α5 subunit. |
| M7898 | Lidoflazine | Lidoflazine is an antianginal calcium channel blocker that carries a significant risk of QT interval prolongation and ventricular arrhythmia. |
| M7897 | L-838,417 | L-838,417 is a novel partial agonist that is ineffective against subtype 1 but has the same efficacy against α2, K3 and α5 subtypes. |
| M7896 | LWH-63 hydrochloride | Non-peptide CRF1 corticotrophin-releasing factor antagonist. |
| M7894 | LY311727 | LY311727 is an oral active compound; Phospholipase A2 (sPLA2; Group activity highlights) inhibitors. |
| M7893 | Leptomycin A | Leptomycins are antifungal antibiotics with unique unsaturated, branched-chain fatty acid structures. |
| M7891 | Lumefantrine | Lumefantrine is an antimalarial compound used to study multiple resistant strains of falciparum malaria. |
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