| 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 |
| M20703 | JHU395 | JHU395 is a novel orally bioavailable GA (glutamine antagonists) prodrug designed to circulate inert in plasma, but permeate and release active GA within target tissues. JHU395 delivers active GA to malignant peripheral nerve sheath tumor (MPNST), and significantly inhibits tumor growth without observed toxicity. |
| M20699 | R-10015 | R-10015 is a potent, selective inhibitor of LIM domain kinase (LIMK) with IC50 of 38 nM for human LIMK1. R-10015 binds to the ATP-binding pocket and acts as a broad-spectrum antiviral compound for HIV infection. |
| M20691 | USP25/28 inhibitor AZ1 | AZ1 is a potent and noncompetitive dual Inhibitors of the ubiquitin-specific protease (USP) 25/28 with IC50s of 0.62 μM and 0.7 μM in Ub-RH110 assay,respectively. |
| M20662 | Demecarium Bromide | Demecarium Bromide (BC-48) is a potent cholinesterase inhibitor, with an apparent affinity (Kiapp) of 0.15 μM. |
| M20661 | Benzylacetone | 4-Phenylbutan-2-one is a model compound for the preparation of fragrances. |
| M20659 | Coumarin 151 | qHTS Assay for Inhibitors of MBNL1-poly(CUG) RNA binding |
| M20657 | Phenylacetaldehyde | Phenylacetaldehyde and carbon monoxide as effective additives for the selective hydrogenation of cyclooctadienes to cyclooctene over palladium catalysts. Phenylacetaldehyde is a oviposition inhibitor for the Pink Bollworm. Phenylacetaldehyde is a fragrant chemical compound, it can attract Moths to bladder flower and to blacklight traps. |
| M20656 | Sequoyitol | Effect on amyloid beta 42 aggregation assessed as inhibition of fiber formation at 5 mM |
| M20655 | 7-Hydroxy-4-methyl-8-nitrocoumarin | Inhibition of CK2 in rat liver |
| M20654 | 6-Hydroxy-4-methylcoumarin | Growth inhibition of human U937 cells by [3H]thymidine incorporation assay |
| M20653 | Huperzine B | Huperzine-B is a efficient inhibitor of human brain AChE. Huperzine-B can enhance ognitive and protect neuro, may be potentially new drug candidates for Alzheimer's disease therapy. |
| M20620 | ONO-7300243 | ONO-7300243 is a novel, potent LPA1(Lysophosphatidic Acid Receptor) antagonist with an IC50 of 160 nM. |
| M20611 | MK571 | MK-571 is a selective, orally active CysLT1 receptor(Cysteinyl leukotriene receptor) antagonist. |
| M20608 | SecinH3 | SecinH3 is a selective cytohesin inhibitor with IC50 of 2.4 μM, 5.4 μM, 5.4 μM, 5.6 μM, 5.6 μM, and 65 μM for hCyh2, hCyh1, mCyh3, hCyh3, drosophila steppke, and yGea2-S7, respectively. |
| M20598 | FPH2 (BRD-9424) | FPH2 (BRD-9424) is a small molecule, which promotes differentiation of iPS-derived hepatocytes. |
| M20585 | Briciclib | Briciclib is a water soluble derivative of ON-013100, a small molecule that binds to and inhibits eukaryotic translation initiation factor 4E (eIF4E) . |
| M20584 | kb-NB77-78 | kb-NB77-78 is an analog of CID797718. However, it shows no inhibitory activty towards PKD1. |
| M20579 | Iso-H7 dihydrochloride | Iso-H7 dihydrochloride is an inhibitor of phosphokinase C . |
| M20569 | Lazabemide | Lazabemide is a reversible and selective inhibitor of monoamine oxidase B (MAO-B) with Ki value of 7.9 nM. |
| M20568 | AGI 1067 | AGI-1067 is a novel, phenolic, intra- and extracellular antioxidant that inhibits the expression of a number of proinflammatory genes involved in atherosclerosis. |
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