| 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. |
| M6395 | Emapunil | Emapunil is a ligand of translocator protein (TSPO, peripheral benzodiazepine receptor). Emapunil exhibits high affinity for TSPO in rat whole brain (Ki = 0.297 nM), and high potency against human and rat glial TSPO (IC50 values are 2.73 and 3.04 nM respectively). |
| M6353 | 6bK | 6bK is a insulin degrading enzyme (IDE) inhibitor. |
| M6298 | Sodium tartrate | Sodium tartrate has been used in organic synthesis to break up emulsions in aqueous workups. The compound is an ingredient of Fehling's solution and of the reagent Biuret (sc-239384). |
| M6265 | BMS 309403 | BMS-309403 is a potent, selective and cell-permeable inhibitor of fatty acid binding protein 4 (FABP4) with a Ki of less than 2 nM. |
| M6252 | Sulbutiamine | Sulbutiamine is a highly lipid soluble synthetic analogue of vitamin B1, used for the treatment of asthenia. |
| M6228 | Wilforine | Wilforine is a sesquiterpene pyridine alkaloid; important bioactive compound in T. wilfordii plants, and is effective in idiopathic pulmonary fibrosis. |
| M6208 | 2-Chloro-5-nitro-benzeneacetic acid | |
| M6207 | FX1 | FX1 is a potent and specific BCL6 inhibitor, with an IC50 of around 35 μM. |
| M6193 | Propacetamol Hydrochloride | Propacetamol is water soluble and can be directly injected. |
| M6192 | Cetilistat | Cetilistat is an inhibitor of pancreatic and gastrointestinal lipases. It has great treatment of obesity in both diabetic and non-diabetic patients. |
| M6188 | QS11 | QS11 is a GTPase activating protein of ADP-ribosylation factor 1 (ARFGAP1) inhibitor. QS11 modulates Wnt/β-catenin signaling through an effect on protein trafficking. QS11 inhibits migration of ARFGAP overexpressing breast cancer cells. |
| M6184 | Dutetrabenazine | Deutetrabenazine is the deuterium labeled Tetrabenazine, which is a VMAT-inhibitor used for the research of hyperkinetic movement disorder. |
| M6147 | M2I-1 | M2I-1 a small Mad2 inhibitor-1. the first small molecule inhibitor targeting the binding of Mad2 to Cdc20, an essential proteinprotein interaction (PPI) within the SAC. |
| M6132 | ECBN HCL | ECBN obtained by the fermentation of Aspergillus nidulans and Aspergillus rugulosus, is known as one of the natural cyclic hexapeptides that have a linoleoyl side chain, which inhibits a crucial enzyme in fungal cell wall biosynthesis, β-(1,3)-d-glucan synthase. |
| M6090 | Cilastatin | Cilastatin (MK0791) is a reversible, competitive renal dehydropeptidase I inhibitor with an IC50 of 0.1 μM. |
| M6082 | 2,6-Dichloro-3,5-dimethoxyaniline | 2,6-Dichloro-3,5-dimethoxyaniline is H3B-6275 intermediate. |
| M6075 | HA15 | HA15 is a molecule that targets specifically BiP/GRP78/HSPA5. HA15 displays anti-cancerous activity on all melanoma cells tested, including cells isolated from patients and cells that developed resistance to BRAF inhibitors. |
| M6062 | DL-Xylose | DL-Xylose is a sugar first isolated from wood. |
| M6030 | Trichlormethiazide | Trichlormethiazide is a diuretic with properties similar to those of hydrochlorothiazide. |
| M6024 | Tranexamic Acid | Tranexamic acid (Transamin) is an antifibrinolytic for blocking lysine-binding sites of plasmin and elastase-derived plasminogen fragments with IC50 of 5 mM. Tranexamic acid attenuates the effects of severe trauma, inhibits urokinase plasminogen activator and ameliorates dry wrinkles. Tranexamic acid can used for the research of hemostasis. |
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