| Structure | Cat No. | Product Name | CAS No. | Product Description |
|---|---|---|---|---|
|
V73808 | 2-Nitrophenyl β-D-glucopyranoside | 2816-24-2 | 2-Nitrophenyl β-D-glucopyranoside is a substrate of β-glucosidase. |
|
V73818 | 5-O-Methylgenistein (Isoprunetin) | 4569-98-6 | 5-O-Mmethylgenistein (Isoprunetin) is an isoflavone that can be extracted from M. |
|
V73814 | 6,8-Dihydroxy-1,2,7-trimethoxy-3-methylanthraquinone | 1622982-59-5 | 6,8-Dihydroxy-1,2,7-trimethoxy-3-methylanthraquinone (compound 1) is an anthraquinone α-glucosidase inhibitor (IC50= 185 μM), which can be extracted from Cassia seeds. |
|
V116065 | Asperilin | 7044-35-1 | Aspirin is an orally effective sesquiterpene lactone with a strong hydroxyl radical scavenging ability. |
|
V73793 | Carpachromene | 57498-96-1 | Carpachromene is a potent α-glucosidase enzyme inhibitor. |
|
V134550 | DSPE-PEG2000-WLSEAGPVVTVRALRGTGSW | DSPE-PEG2000-WLSEAGPVVTVRALRGTGSW is a polypeptide that targets Tenascin-X and can be conjugated to liposomes and exosomes. | |
|
V88495 | GPX4-IN-11 | 951570-56-2 | GPX4-IN-11 (compound I14) is a potent inhibitor of GPX4 with a KD of 45.7 μM. |
|
V84205 | GPX4-IN-8 | 2703776-20-7 | |
|
V111348 | iMQT_020 | 2463893-46-9 | iMQT_020 is a selective allosteric SLC1A5_var inhibitor. |
|
V73780 | Kaempferol-7-O-rhamnoside | 20196-89-8 | Kaempferol-7-O-rhamnoside is extracted from the leaves of Chimonanthus nitens Oliv and is a potent inhibitor of α-glucosidase activity. |
|
V140388 | MPO-IN-10 | 2922402-01-3 | MPO-IN-10 is an orally effective, selective, and irreversible myeloperoxidase (MPO) inhibitor with an IC50 value of 0.080 μM for human MPO. |
|
V117202 | Myeloperoxidase, Human Neutrophil | Human neutrophil myeloperoxidase is a type of peroxidase. | |
|
V73826 | N-Acetyl lysyltyrosylcysteine amide | 1287585-40-3 | N-Acetyl lysyltyrosylcysteine amide is a potent, reversible, specific and nontoxic tripeptide inhibitor of myeloperoxidase (MPO). |
|
V4475 | PF-06282999 | 1435467-37-0 | PF-06282999 is a novel, potent and selectivemyeloperoxidase(MPO)inhibitor with the potential for the treatment of cardiovascular diseases. |
|
V118478 | RSL3-NH2 | 3051815-39-2 | RSL3-NH2 is a GPX4 inhibitor and ferroptosis inducer. |
|
V145087 | SNT-8370 | SNT-8370 is an orally effective VAP-1 (IC50: 10 nM) and myeloperoxidase (MPO) (IC50: 17 nM) inhibitor, with an inhibitory efficacy against VAP-1 and MPO that is 100-1000 times higher than that against other mammalian (per)oxidases. | |
|
V145350 | STIM1-TFR1-IN-1 | 2196106-61-1 | STIM1-TFR1-IN-1 is an orally effective inhibitor of the matrix-interacting molecule 1 (STIM1)-transferrin receptor 1 (TFR1) protein complex with a dissociation constant (Kd) of 2.18 μM for STIM1-CD protein. |
|
V73809 | α-Glucosidase-IN-14 | 2816072-15-6 | α-Glucosidase-IN-14 (compound 5) is a potent α-glucosidase inhibitor (antagonist) with IC50 of 5.22 μM. |
|
V73791 | α-Glucosidase-IN-17 | 2820424-84-6 | α-Glucosidase-IN-17 (Compound 12B) is a potent, orally bioactive α-glucosidase inhibitor (antagonist) with IC50 of 3.79 μM. |
|
V73811 | α-Glucosidase-IN-28 | 2949513-10-2 | α-Glucosidase-IN-28 (Compound 18) is an α-Glucosidase inhibitor (IC50= 0.62 μM, Ki: 3.93μM). |