| 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. |
| M56602 | SACLAC | SACLAC, a Ceramide analog, is a potent and covalent acid ceramidase (ASAH1; AC) inhibitor with a Ki of 97.1 nM. |
| M56601 | Acid Ceramidase-IN-1 | Acid Ceramidase-IN-1 is a potent and oral bioavailable acid ceramidase (AC, ASAH-1) inhibitor (hAC IC50=0.166 μM). |
| M56596 | Carboxylesterase-IN-2 | Carboxylesterase-IN-2 is a potent inhibitor of Carboxylesterase Notum with an IC50 less than or equal to 10 nM. |
| M56590 | GlyRS-IN-1 | GlyRS-IN-1 is a glycyl-tRNA synthase (GlyRS) inhibitor. |
| M56583 | UT-B-IN-1 | UT-B-IN-1 (UTBINH-14) is a reversible, competitive and selective urea transporter-B (UT-B) inhibitor with IC50 values of 10 and 25 nM for human and mouse UT-B, respectively. |
| M56519 | Benzamil | Benzamil (Benzylamiloride), an Amiloride analogue, is a Na+/Ca2+ exchanger (NCX) inhibitor (IC50~100 nM). |
| M56466 | CRAC intermediate 2 | CRAC intermediate 2 is a intermediate compound for CRAC inhibitor synthesis. |
| M56464 | RO2959 monohydrochloride | RO2959 monohydrochloride is a potent and selective CRAC channel inhibitor with an IC50 of 402 nM. |
| M56460 | Encecalinol | Encecalinol, extracted from aerial parts of Ageratina grandifolia, is a potent inhibitor of calmodulin inhibitor. |
| M56459 | Beauverolide Ja | Beauverolide Ja, a cyclotetradepsipeptide, is a potent calmodulin (CaM) inhibitor with a Kd of 0.078 μM and a Ki of 0.39 μM for Ca2+-CaM. |
| M56439 | MLKL-IN-2 | MLKL-IN-2 is a MLKL inhibitor. |
| M56391 | KF38789 | KF38789 is a selective inhibitor of P-selectin-PSGL-1 binding. |
| M56386 | PSB-06126 | PSB-06126 is a selective nucleoside triphosphate diphosphohydrolase (NTPDase) inhibitor, with the Ki values of 0.33 μM for rat NTPDase 1, 19.1 μM for NTPDase 2 and 2.22 μM for NTPDase 3, respectively. |
| M56342 | MethADP disodium | MethADP disodium is a specific CD73 inhibitor. |
| M56341 | MethADP sodium | MethADP (sodium salt) (Adenosine 5'-(α,β-methylene)diphosphate (sodium)) is a specific CD73 inhibitor. |
| M56334 | SB-706375 | SB-706375 is an antagonist of the Urotensin II (UII) receptor. |
| M56279 | EM574 | EM574 is a potent motilin receptor agonist in the human gastric antrum and rabbit gastrointestinal tract in vitro. |
| M56257 | GW-803430 | GW-803430 (GW-3430) is a potent and selective melanin-concentrating hormone receptor 1 (MCH R1) antagonist with a pIC50 of 9.3. |
| M56192 | BAY-27-9955 | BAY-27-9955 is an orally active non-peptide glucagon receptor antagonist. |
| M56191 | Orforglipron hemicalcium hydrate | Orforglipron hemicalcium hydrate (LY3502970 hemicalcium hydrate; GLP-1 receptor agonist 1 hemicalcium hydrate) is the calcium salt hydrate form of Orforglipron. |
Products are for research use only. Not for human use. We do not sell to patients.
© Copyright 2010-2026 AbMole BioScience. All Rights Reserved.
