| 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. |
| M8793 | Tocainide hydrochloride | Tocainide hydrochloride is a sodium channel blocker; Class IB antiarrhythmic. |
| M8792 | TD52 | TD52, an erlotinib analog, is a putative inhibitor of CIP2A that exhibits potent antitumor efficacy on HCC and TNBC cells. |
| M8791 | TB5 | TB5 is a potent and selective reversible inhibitor of monoamine oxidase B (MAOB) with a Ki value of 110 nM. |
| M8790 | MDL-860 | MDL-860 is a 5-nitro-2-phenoxybenzonit |
| M8786 | Roflupram | Roflupram (FFPM) is a potent anti-inflammatory phosphodiesterase 4 (PDE4) inhibitor that was found to suppress inflammasome activation in microglial cells by enhancing autophagy. |
| M8785 | Fosamprenavir calcium | Fosamprenavir calcium is an HIV protease inhibitor anti-retroviral. |
| M8782 | NAMI-A | NAMI-A is a potent antimetastatic compound in vivo that is exhibits little cytotoxicity towards many cancer cell lines. |
| M8778 | ZD0947 | ZD0947 is potent ATP-sensitive K+ channels (KATP channels) opener. |
| M8776 | ARM390 | ARM390 in a δ-selective opioid receptor agonist derivative of SNC80. |
| M8773 | Liarozole dihydrochloride | Liarozole (R 75251, R75,251) is an orally active benzimidazole-based retinoic acid (RA) metabolism blocking agent (RAMBA) that targets multiple P450 enzymes, including aromatase (CYP19), 17-hydroxylase/17,20-lyas |
| M8772 | SAK3 | SAK3 is a potent and orally active spiroimidazopyridine derivative that enhances Cav3. |
| M8771 | SR2595 | SR2595 is an inverse agonist of PPARG (PPARγ) with an IC50 value of 30 nM. |
| M8768 | TUG-1387 | TUG-1387 is a close structural analog of AH-7614 that lacks activity at FFA4 that can serve as negative control. |
| M8767 | MIND4-17 | MIND4-17 is a potent NRF2 (nuclear factor erythroid 2-related factor 2) activator that covalently modifies a critical stress-sensor cysteine (C151) in the BTB domain of the E3 ligase substrate adaptor protein Kelch-like ECH-associated protein 1 (KEAP1), the primary negative regulator of NRF2. |
| M8763 | Tiotropium bromide monohydrate | Tiotropium Bromide is an anticholinergic broncholidator. |
| M8759 | PS432 | PS432 is an allosteric inhibitor of Protein Kinase C (PKC) that targets regulatory site (PIF-pocket) present in the kinase domain. |
| M8757 | TASIN-1 hydrochloride | TASIN-1 (Truncated APC Selective INhibitor-1) targets EBP- (Emopamil-binding protein; D8-D7 sterol isomerase) dependent cholesterol biosynthesis and selectively induces cellular cholesterol depletion and apoptotic death in human colorectal cancer (CRC) cultures harboring APC truncations under lipid-deficient conditions (0. |
| M8756 | GSK9311 | GSK9311 is a negative control for the SGC epigenetic probe GSK6853. |
| M8754 | Linoleamide | Linoleamide is an endogenous primary fatty acid amide (PFAM) signaling lipid that modulates intracellular Ca2+ homeostasis. |
| M8753 | PKUMDL-WQ-2201 | PKUMDL-WQ-2201 is a potent and selective non-NAD+-competing allosteric inhibitor of phosphoglycerate dehydrogenase (PHGDH) that selectively inhibits serine synthesis in cancer cells. |
Products are for research use only. Not for human use. We do not sell to patients.
© Copyright 2010-2026 AbMole BioScience. All Rights Reserved.
