| 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. |
| M7125 | PF 945863 | PF 945863 is a macrolide antibiotic. |
| M7124 | PF 750 | PF 750 is a selective FAAH inhibitor. |
| M7121 | PF 4778574 | PF 4778574 is a positive allosteric modulator of AMPA receptors. |
| M7118 | PF 06273340 | PF 06273340 is a potent and selective pan-Trk inhibitor; peripherally restricted. |
| M7117 | PF 05190457 | PF 05190457 is a high affinity and selective ghrelin receptor inverse agonist. |
| M7114 | PF 04449613 | PF 04449613 is a potent PDE9 inhibitor; brain penetrant. |
| M7113 | PF 04217903 mesylate | PF 04217903 mesylate is a highly selective MET inhibitor. |
| M7109 | Penitrem A | Penitrem A is a potent and selective BK Ca (K Ca1.1) channel blocker. |
| M7107 | PD 90780 | PD 90780 is a inhibits NGF binding to p75 NTR . |
| M7105 | PD 158780 | PD 158780 is a potent ErbB receptor family inhibitor. |
| M7101 | Palmitoylisopropylamide | Palmitoylisopropylamide is a inhibitor of FAAH. |
| M7099 | PACMA 31 | PACMA 31 is a irreversible protein disulfide isomerase (PDI) inhibitor. |
| M7098 | PACAP 1-27 | PACAP 1-27 is a potent stimulator of adenylyl cyclase. |
| M7096 | P1075 | P1075 is a potent K ir6 (K ATP) channel opener. |
| M7095 | Ozagrel hydrochloride | Ozagrel hydrochloride is a selective thromboxane A 2 synthetase inhibitor. |
| M7093 | OXSI 2 | OXSI 2 is a potent Syk kinase inhibitor; also inhibits assembly of NLRP3 inflammasomes. |
| M7092 | Oxotremorine sesquifumarate | Oxotremorine sesquifumarate is a muscarinic agonist. |
| M7091 | Org 48762-0 | Org 48762-0 is a selective p38α/β inhibitor; orally bioavailable. |
| M7090 | Org 37684 | Org 37684 is a 5-HT 2 agonist. |
| M7089 | Org 25543 hydrochloride | Org 25543 hydrochloride is a potent and selective GlyT2 inhibitor. |
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