
Aminopeptidase
Aminopeptidases are a group of enzymes that catalyze the cleavage of amino acids from the N-terminus of peptides and proteins, playing a crucial role in protein maturation and degradation. These enzymes are involved in various physiological processes, including antigen processing, peptide hormone regulation, and cellular homeostasis. Inhibitors of aminopeptidases are of interest in the treatment of diseases such as cancer, inflammation, and infectious diseases. At CymitQuimica, we provide a variety of aminopeptidase inhibitors to support your research in proteomics, drug development, and disease treatment.
Found 67 products of "Aminopeptidase"
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Leucinal
CAS:<p>Leucinal inhibits the activity of brain aminopeptidase and potentiates analgesia induced by leu-enkephalen.</p>Formula:C6H13NOColor and Shape:SolidMolecular weight:115.17M8891
CAS:<p>M8891: Oral, reversible MetAP-2 inhibitor, brain-penetrant (IC50: 54nM; Ki: 4.33nM), hinders endothelial & tumor cell growth, antiangiogenic & antitumor.</p>Formula:C20H17F2N3O3Color and Shape:SolidMolecular weight:385.36HFI-437
CAS:<p>HFI-437 is a potent, non-peptidic, insulin-regulated aminopeptidase (IRAP) inhibitor with a K i of 20 nM and functions as a cognitive enhancer [1].</p>Formula:C23H20N2O5Color and Shape:SolidMolecular weight:404.42Amastatin
CAS:<p>Amastatin is a non-toxic inhibitor of aminopeptidase A and leucine aminopeptidase, and its Ki for aminopeptidase A is 1 μM .</p>Formula:C21H38N4O8Purity:98%Color and Shape:SolidMolecular weight:474.55Aminopeptidase-IN-1
CAS:<p>Aminopeptidase-IN-1: potent IRAP blocker, Ki 7.7 μM, useful for cognitive/memory disorder research.</p>Formula:C18H16N2O6Purity:98.37%Color and Shape:SolidMolecular weight:356.33SC-22716
CAS:<p>SC-22716 is a LTA4 hydrolase inhibitor.SC-22716 has anti-inflammatory activity and may be used in the study of inflammatory bowel disease and psoriasis.</p>Formula:C18H21NOPurity:99.91%Color and Shape:SolidMolecular weight:267.37TP-004
CAS:<p>TP-004 is a potent and reversible methionine aminopeptidase 2 (MetAP2) inhibitor (IC50: 6 nM).</p>Formula:C17H16F3N5OPurity:98%Color and Shape:SolidMolecular weight:363.34BDM14471
CAS:<p>BDM14471 is a selective inhibitor of hydroxamate PfAM1.</p>Formula:C17H15FN2O3Purity:98%Color and Shape:SolidMolecular weight:314.31LYS006
CAS:<p>LYS006 is a highly efficient and selective LTA4H (leukotriene A4 hydrolase) inhibitor,for neutrophil-driven inflammatory diseases ulcerative colitis.</p>Formula:C16H14ClFN6O3Purity:99.33%Color and Shape:SoildMolecular weight:392.77JNJ-40929837
CAS:<p>JNJ-40929837 is an oral inhibitor of LTA4 hydrolase, which catalyzes LTB4 production.</p>Formula:C22H24N4O2SColor and Shape:SolidMolecular weight:408.52RB 101
CAS:<p>RB 101 suppresses enkephalinase and aminopeptidases; biologically cleaved at disulfide to produce inhibitors of both aminopeptidase N and neutral endopeptidase.</p>Formula:C31H38N2O3S3Purity:98%Color and Shape:SolidMolecular weight:582.84MetAP2-IN-1
CAS:<p>MetAP2-IN-1 is a selective inhibitor of MetAP2, a target involved in angiogenesis-related conditions, suitable for research applications [1].</p>Formula:C8H6BrN3Purity:98%Color and Shape:SolidMolecular weight:224.06Arphamenine A
CAS:<p>Arphamenine A is an inhibitor of aminopeptidase B (aminopeptidaseB) found in HMG361-CF4 of Actinomadura azurea. It exhibits inhibitory effects against Sarcoma 180 and invasive micropapillary carcinoma (IMC).</p>Formula:C16H24N4O3Color and Shape:SolidMolecular weight:320.387A-800141
CAS:<p>A-800141 is an orally active and selective MetAP2 inhibitor with an IC50 of 12 nM, while showing weaker inhibitory activity against MetAP1 (IC50: 36 μM). GAPDH can serve as a biomarker for monitoring the inhibition of MetAP2 by A-800141. This compound exhibits anti-angiogenic and anticancer properties in various xenograft tumor models.</p>Formula:C24H30N2O4SColor and Shape:SolidMolecular weight:442.571EC33
CAS:<p>EC33, a selective aminopeptidase A (APA) inhibitor, blocks the pressor response of exogenous Ang II and does not cross the blood-brain barrier, making it a potential candidate for salt-dependent hypertension research [1].</p>Formula:C4H11NO3S2Color and Shape:SolidMolecular weight:185.27LTA4H-IN-3
CAS:<p>LTA4H-IN-3 (compound 9) functions as an inhibitor of LTA4H, demonstrating an IC50 of 28 nM [1].</p>Formula:C17H15ClN4O3Color and Shape:SolidMolecular weight:358.78LTA4H-IN-2
CAS:<p>LTA4H-IN-2 (compound (S)-2) acts as an orally active inhibitor targeting Leukotriene A4 Hydrolase, exhibiting potent activity with an IC 50 of less than 3 nM [1].</p>Formula:C20H19FN6O2Color and Shape:SolidMolecular weight:394.4Bestatin methyl ester
CAS:<p>Bestatin methyl ester (600, 900 µM; 24 h) inhibits spore cell differentiation in Dictyostelium discoideum.</p>Formula:C17H26N2O4Color and Shape:SolidMolecular weight:322.4Ketomethylenebestatin
CAS:<p>Ketomethylenebestatin, a weaker carba-analog of aminopeptidase inhibitor bestatin, is 10x less potent.</p>Formula:C17H25NO4Purity:98%Color and Shape:SolidMolecular weight:307.38SDX-7539
CAS:<p>SDX-7539 is a selective MetAP2 inhibitor that inhibits the proliferation of HUVEC, with an IC50 of 120 μM. It has demonstrated antitumor activity in xenografted NSCLC in athymic nude mice.</p>Formula:C23H38N2O5Molecular weight:422.56

