| 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. |
| M9669 | 1H-pyrazolo[1,5-a]pyridin-5-one | 1H-pyrazolo[1,5-a]pyridin-5-one |
| M9668 | 6-chloropyrido[3,2-d]pyrimidine-2,4-diamine | 6-chloropyrido[3,2-d]pyrimidine-2,4-diamine |
| M9666 | 2,4-dichloro-5,7-dimethoxyquinoline | 2,4-dichloro-5,7-dimethoxyquinoline |
| M9660 | Bis(triphenylphosphine)palladium(II) dichloride | Bis(triphenylphosphine)palladium(II) dichloride |
| M9658 | 1-Bromo-4-(1-fluorovinyl)benzene | 1-Bromo-4-(1-fluorovinyl)benzene |
| M9657 | 7-Bromoquinoline-4-carboxylic acid | 7-Bromoquinoline-4-carboxylic acid |
| M9629 | 5-Methoxyquinolin-8-amine | 5-Methoxyquinolin-8-amine is a new cyclic peptide compounds with good pharmaceutical properties. |
| M8870 | Zopolrestat | Zopolrestat is an inhibitor of Aldose Reductase. |
| M8865 | Zimelidine dihydrochloride | Serotonin transport blocker; Antidepressant compounds. |
| M8858 | XE-991 | XE-991 is a KCNQ channel blocker; which is more potent than linopiridine. |
| M8855 | WR99210 | WR99210 is a potent inhibitor of Plasmodium falciparum dihydrofolate reductase (DHFR), which is a major malarial drug target. |
| M8853 | WIN 62,577 | Non-peptide NK1 tachykinin receptor antagonist. |
| M8852 | W-84 dibromide | Potent allosteric modulator of M2 muscarinic acetylcholine receptors. |
| M8851 | WAY 161503 hydrochloride | The 5-HT2C receptors have been implicated in conditions including obesity, anxiety, depression, OCD, schizophrenia, migraine, nociception and erectile dysfunction. |
| M8848 | VU0152100 | Positive allosteric modulator of muscarinic choline receptor M4. |
| M8844 | Valeryl Salicylate | Selective, irreversible COX-1 inhibitor. |
| M8843 | Verrucarol | Trichothecene mycotoxin that is a component of toxic mold. |
| M8841 | Carboxytolbutamide | In vivo tolbutamide metabolite. |
| M8839 | U-74389G | Free radical lipid peroxidation inhibitor in cultured brain cells, monocytic THP1 cells, and LLC-PK1 cell layers. |
| M8835 | UA62784 | Studies have also reported that UA62784 associates with tubulin at or near the colchicine-binding sites in cells and functions as a cytotoxic, microtubule inhibitor. |
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