| 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 |
| M3896 | Ro 48-8071 | Ro 48-8071 is an inhibitor of OSC(Oxidosqualene cyclase; IC50=6.5 nM) that has low-density lipoprotein (LDL) cholesterol lowering activity. |
| M3877 | 4-Chloro-3-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridine | 4-Chloro-3-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridine |
| M3876 | 6-bromo-4-methoxypyrazolo[1,5-a]pyridine-3-carbonitrile | 6-bromo-4-methoxypyrazolo[1,5-a]pyridine-3-carbonitrile |
| M3869 | Calcium sulfate dihydrate | Calcium sulfate dihydrate |
| M3817 | Methoxypolyethylene glycol maleimide | Methoxypolyethylene glycol maleimide (MeO-PEG-Mal) is used as a protein pegylation reagent. |
| M3816 | Uridine triphosphate trisodium | Uridine triphosphate trisodium (UTP;Uridine 5'-triphosphate) is a nucleotide. |
| M3793 | Deferitrin | Deferitrin is a desferrioxanthin (DFT) analog as well as an orally active iron chelator.D may be used in studies related to severe β-thalassemia. |
| M3761 | TH-237A | TH-237A is a novel neuroprotective agent, which possess protective properties against β-amyloid (Aβ)-induced neurodegeneration associated with Alzheimer's disease. |
| M3709 | APY29 | APY29 is a highly potent and selective small molecule modulator of IRE1α . |
| M3690 | Mefloquine hydrochloride | Mefloquine hydrochloride is a quinoline antimalarial inhibitor that is structurally related to the antiarrhythmic agent quinidine. |
| M3688 | SP-420 | SP-420 is an orally active small molecule that selectively binds iron and removes it from the body. |
| M3647 | HJC0350 | HJC0350 is a potent and selective EPAC2 inhibitor with IC50 of 0.3 μM, exhibiting no inhibition on Epac1. |
| M3597 | Fudosteine | Fudosteine is a novel mucoactive agent and a MUC5AC mucin hypersecretion inhibitor. |
| M3547 | Glibenclamide | Glibenclamide (Glyburide) is an orally active ATP-sensitive K+ channel (KATP) inhibitor. Glibenclamide inhibits P-glycoprotein. Glibenclamide directly binds and blocks the SUR1 subunits of KATP and inhibits the cystic fibrosis transmembrane conductance regulator protein (CFTR). |
| M3544 | Loteprednol etabonate | Loteprednol etabonate is an anti-inflammatory corticosteroid used in ophthalmology. |
| M3469 | Prednisone | Prednisone (Adasone) is a synthetic corticosteroid agent that is particularly effective as an immunosuppressant compound. |
| M3465 | Triamcinolone | Triamcinolone is a long-acting corticosteroid. Triamcinolone is a corticosteroid hormone receptor (GCR) agonist and an anti-inflammatory agent. |
| M3459 | Lubiprostone | Lubiprostone is a gastrointestinal agent used for the treatment of idiopathic chronic constipation. |
| M3443 | CP-91149 | CP-91149 is a selective glycogen phosphorylase (GP) inhibitor with IC50 of 0.13 μM in the presence of glucose, 5- to 10-fold less potent in the absence of glucose. |
| M3423 | Warfarin sodium | Warfarin sodium, an anticoagulant that acts by inhibiting the synthesis of vitamin K-dependent coagulation factors. |
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