Aminopeptidase
Les aminopeptidases sont un groupe d'enzymes qui catalysent la coupure des acides aminés à partir de l'extrémité N-terminale des peptides et des protéines, jouant un rôle crucial dans la maturation et la dégradation des protéines. Ces enzymes sont impliquées dans divers processus physiologiques, notamment le traitement des antigènes, la régulation des hormones peptidiques et l'homéostasie cellulaire. Les inhibiteurs des aminopeptidases présentent un intérêt pour le traitement de maladies telles que le cancer, l'inflammation et les maladies infectieuses. Chez CymitQuimica, nous proposons une variété d'inhibiteurs d'aminopeptidases pour soutenir vos recherches en protéomique, développement de médicaments et traitement des maladies.
67 produits trouvés pour "Aminopeptidase"
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Leucinal
CAS :<p>Leucinal inhibits the activity of brain aminopeptidase and potentiates analgesia induced by leu-enkephalen.</p>Formule :C6H13NOCouleur et forme :SolidMasse moléculaire :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>Formule :C20H17F2N3O3Couleur et forme :SolidMasse moléculaire :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>Formule :C23H20N2O5Couleur et forme :SolidMasse moléculaire :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>Formule :C21H38N4O8Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :474.55Aminopeptidase-IN-1
CAS :<p>Aminopeptidase-IN-1: potent IRAP blocker, Ki 7.7 μM, useful for cognitive/memory disorder research.</p>Formule :C18H16N2O6Degré de pureté :98.37%Couleur et forme :SolidMasse moléculaire :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>Formule :C18H21NODegré de pureté :99.91%Couleur et forme :SolidMasse moléculaire :267.37TP-004
CAS :<p>TP-004 is a potent and reversible methionine aminopeptidase 2 (MetAP2) inhibitor (IC50: 6 nM).</p>Formule :C17H16F3N5ODegré de pureté :98%Couleur et forme :SolidMasse moléculaire :363.34BDM14471
CAS :<p>BDM14471 is a selective inhibitor of hydroxamate PfAM1.</p>Formule :C17H15FN2O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :314.31LYS006
CAS :<p>LYS006 is a highly efficient and selective LTA4H (leukotriene A4 hydrolase) inhibitor,for neutrophil-driven inflammatory diseases ulcerative colitis.</p>Formule :C16H14ClFN6O3Degré de pureté :99.33%Couleur et forme :SoildMasse moléculaire :392.77JNJ-40929837
CAS :<p>JNJ-40929837 is an oral inhibitor of LTA4 hydrolase, which catalyzes LTB4 production.</p>Formule :C22H24N4O2SCouleur et forme :SolidMasse moléculaire :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>Formule :C31H38N2O3S3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :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>Formule :C8H6BrN3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :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>Formule :C16H24N4O3Couleur et forme :SolidMasse moléculaire :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>Formule :C24H30N2O4SCouleur et forme :SolidMasse moléculaire :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>Formule :C4H11NO3S2Couleur et forme :SolidMasse moléculaire :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>Formule :C17H15ClN4O3Couleur et forme :SolidMasse moléculaire :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>Formule :C20H19FN6O2Couleur et forme :SolidMasse moléculaire :394.4Bestatin methyl ester
CAS :<p>Bestatin methyl ester (600, 900 µM; 24 h) inhibits spore cell differentiation in Dictyostelium discoideum.</p>Formule :C17H26N2O4Couleur et forme :SolidMasse moléculaire :322.4Ketomethylenebestatin
CAS :<p>Ketomethylenebestatin, a weaker carba-analog of aminopeptidase inhibitor bestatin, is 10x less potent.</p>Formule :C17H25NO4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :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>Formule :C23H38N2O5Masse moléculaire :422.56
