| 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 |
| M7731 | CHIC-35 | CHIC-35 is cell-permeable, metabolically stable, and very potent inhibitor of SIRT1; IC50 of S-isomer is 60 nM; IC50 of mixed isomers is 124 nM. |
| M7725 | CK-548 | CK-548 inhibits the activity of actin-related protein (Arp)2/3 complex by inserting into the hydrophobic core of Arp3 and altering its conformation: inhibits. |
| M7724 | CAY10397 | Potent and selective inhibitor of 15-hydroxyprostaglandin dehydrogenase (15-hydroxy-PGDH). |
| M7723 | CBIQ | CBIQ is an activator of the cystic fibrosis transmembrane conductance regulator (CFTR) and the intermediate-conductance calcium-sensitive K+ channel (KCNN4). |
| M7722 | Ciproxifan hydrochloride | Ciproxifan belongs to a novel chemical series of histamine H3-receptor antagonists. |
| M7721 | Chrysomycin B | Antibiotic from Streptomyces sp. |
| M7717 | CGP 52608 | CGP 52608 is a specific activator of retinoic acid receptor-related orphan receptor α (RORA). |
| M7716 | CIL-102 | CIL-102 is a tubulin polymerization inhibitor: apoptosis inducer. |
| M7714 | Cinnarizine | Ca2+ channel blocker; central and peripheral vasodilator. |
| M7712 | Cisapride monohydrate | 5-HT4 serotonin receptor agonist. |
| M7711 | Cloricromene | Antithrombotic coumarin derivative that inhibits platelet and leukocyte function and suppresses arachidonic acid liberation by interfering with PLA2 activation. |
| M7710 | 9-Cyclopentyladenine monomethanesulfonate | A stable, cell-permeable, non-competitive adenylyl cyclase inhibitor that targets the P-site domain. |
| M7708 | CPNQ | Misfolded proteins accumulate in many neurodegenerative diseases, including huntingtin in Huntington′s disease and alpha-synuclein in Parkinson′s disease. |
| M7705 | Cyclazosin hydrochloride | α1B-adrenoceptor antagonist. |
| M7703 | Clofilium tosylate | K+ channel blocker; cardiac depressant; anti-arrhythmic. |
| M7697 | Chlorprothixene hydrochloride | D2 dopamine receptor antagonist; blocks a subset of GABAA receptors in rat cortex that is also blocked by clozapine; thioxanthine antipsychotic. |
| M7695 | CGS-9343B | CGS-9343B is a selective calmodulin antagonist with minimal protein kinase C or antidopaminergic activity. |
| M7694 | Cibenzoline succinate | Dibenzazoline is a class IA antiarrhythmic compound. |
| M7689 | Caroverine hydrochloride | Caroverine hydrochloride is a nonselective NMDA and AMPA glutamate receptor antagonist. |
| M7688 | Chrysamine G | New probe for ß-amyloid aggregates. |
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