| 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. |
| M57011 | Ethiazide | Ethiazide is a thiazole diuretic which inhibits renal reabsorption of sodium and water, thereby increasing urine excretion, reducing fluid retention, and lowering blood volume and blood pressure. |
| M57010 | GV-150013 | GV-150013 is a selective CCK-B receptor antagonist. |
| M57009 | AR-C67085 | AR-C67085 (PSB 0413; FPL 67085) is a potent platelet P2T receptor antagonist with an pIC50 value of 8.60. |
| M57008 | AS1134900 | AS1134900 is a highly selective, allosteric and uncompetitive NADP+-dependent malic enzyme 1 (ME1) inhibitor. |
| M57007 | TNIK-IN-7 | TNIK-IN-7 is an inhibitor of Traf2 and Nck-interacting kinase (TNIK), with IC50 of 11 nM, that has antitumor activity. |
| M57006 | NBD-amine | NBD-amine is a fluorogenic amine. |
| M57005 | CBM-301940 | CBM-301940 is an orally active malonate CoA decarboxylase (MCD) inhibitor with IC50 value of 23 nM. |
| M57004 | WAY-639872 | WAY-639872 is an active molecule. |
| M57003 | A 410099.1 | A 410099.1 is a BIRC inhibitor, with EC50 values for BIRC2, BIRC3, BIRC4, BIRC7, and BIRC8 are 4.6, 9.2, 15.6, 19.9, and 93.9 nM, respectively. |
| M57002 | WAY-309236 | WAY-309236 is an active molecule for the study of amyloid diseases and synucleinopathies. |
| M57001 | Centhaquin | Centhaquine (Centhaquin; PMZ-2010) is a novel agent has the potential for treatment of haemorrhagic shock. |
| M57000 | Rimexolone | Rimexolone (Org 6216) is a glucocorticoid steroid with anti-inflammatory activity. |
| M56999 | Aviglycine | Aviglycine (ABG-3168 free base) is an inhibitor of ethylene biosynthesis. |
| M56998 | Bumadizone | Bumadizone is a non-steroidal anti-inflammatory drug (NSAID) and can relieve pain. |
| M56997 | Sugammadex | Sugammadex is a synthetic γ-cyclodextrin derivative, and acts as a reversal agent for neuromuscular block. |
| M56996 | Sagopilone | Sagopilone (ZK-EPO) demonstrated antitumor activity in human orthotopic glioma models both in vitro and in vivo. |
| M56995 | Dipropofol | Dipropofol is an antioxidant agent. |
| M56994 | SARM1-IN-2 | SARM1-IN-2 is a SARM1 inhibitor. |
| M56992 | Proquazone | Proquazone (RU 43-715) is a chemically distinctive non-steroidal anti-inflammatory agent (NSAID). |
| M56991 | Buthiazide | Buthiazide (Butizide) is a diuretic compound that can be used for high blood pressure research. |
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