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9
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T9345 |
Aminopeptidase M
|
Others | Others |
Aminopeptidase M 抑制对多种疾病(例如高度血管化的癌症类型)具有重要意义。 | |||
T61278 |
Aminopeptidase-IN-1
|
Aminopeptidase | Metabolism |
Aminopeptidase-IN-1 是一种有效的胰岛素调节氨肽酶 (IRAP) 抑制剂(Ki: 7.7 μM)。Aminopeptidase-IN-1 可用于认知和记忆障碍的研究。 | |||
T36943 | Aminopeptidase N Inhibitor | ||
Aminopeptidase N (AP-N) inhibitor is a reversible inhibitor of AP-N/CD13 (IC50 = 25 μM). It is selective for AP-N/CD13 over matrix metalloproteinase-9 (MMP-9), angiotensin converting enzyme (ACE), neutral endopeptidase (NEP), γ-glutamyl transpeptidase, and the serine proteases dipeptidyl peptidase 4 (DPP-4) and cathepsin G at a concentration of 1 mM. AP-N inhibitor is non-cytotoxic to U937 cells at a concentration of 100 μM. | |||
TQ0047 |
DG051
|
Aminopeptidase | Metabolism |
DG051 是有效的白三烯 A4 水解酶抑制剂,IC50=47 nM。 | |||
T76568 |
Aminopeptidase N Ligand (CD13) NGR peptide
|
||
AminopeptidaseN Ligand (CD13) NGR peptide 是靶向CD13的多肽,常见于癌症研究中,用作细胞内传递的载体介质。 | |||
T21859 |
ARM1
|
Aminopeptidase; Epoxide Hydrolase | Metabolism |
ARM1 是氨基肽酶和环氧化物水解酶抑制剂,IC50分别为为7.61 µM 和12.4 µM。 | |||
T11221 |
ERAP1-IN-1
|
Others | Others |
ERAP1-in-1 是一种内质网氨基肽酶 1 (ERAP1) 抑制剂,能竞争性地抑制 ERAP1 对代表性生物底物九聚物肽的作用。 | |||
T6301 |
Tosedostat
CHR-2797,托舍多特 |
Aminopeptidase; AChR | Metabolism; Neuroscience |
Tosedostat (CHR-2797) 是一种具有口服活性的氨基肽酶(aminopeptidase) 抑制剂,对多种肿瘤细胞系均具有抗增殖作用。 | |||
T3715 |
Acebilustat
阿西鲁司特,CTX-4430 |
Aminopeptidase; LTR | Immunology/Inflammation; Metabolism |
Acebilustat (CTX-4430) 是一种具有口服活性的白三烯 A4 水解酶抑制剂,可用于炎症研究。 | |||
T16684 |
Puromycin aminonucleoside
维生素E醋酸酯,NSC 3056 |
Apoptosis; Proteasome; Aminopeptidase; Antibacterial; Antibiotic | Apoptosis; Metabolism; Microbiology/Virology; Proteases/Proteasome; Ubiquitination |
Puromycin aminonucleoside (NSC-3056) 是一种氨基核苷类抗生素,是嘌呤霉素类似物。它可逆抑制二肽基肽酶和胞浆丙氨酸氨基肽酶。它通过以氧化应激依赖性方式调节 ZO-1 来增加足细胞通透性。它诱导细胞凋亡 。 | |||
T28482 |
Firibastat
QGC 001,QGC-001,RB-150,RB150,QGC001,RB 150 |
Aminopeptidase | Metabolism |
Firibastat (RB150) 是一种具有口服活性的 EC33 前体药物。Firibastat 是一种首创的脑氨基肽酶 A(APA) 抑制剂 (Ki=200 nM),选择性地抑制高血压大鼠脑血管紧张素 II 转化为血管紧张素 III,降低血压。 | |||
T21696 |
SC-57461A
N -甲基- N -[3 - [4 - (苯甲基)苯氧基]丙基Β-丙氨酸盐酸盐 |
Aminopeptidase | Metabolism |
SC-57461A 是一种口服有活力的非肽类白三烯 A4 (LTA4) 水解酶选择性抑制剂,它能够抑制重组人 (IC50: 2.5 nM) 、小鼠 (IC50: 3 nM) 和小鼠LTA4水解酶 (IC50: 23 nM) 。 | |||
TP1181 |
Bradykinin (2-9)
Des-Arg1-bradykinin |
Bradykinin Receptor | GPCR/G Protein |
Bradykinin (2-9) (Des-Arg1-bradykinin),是Bradykinin的一种氨基端截短肽类代谢物,通过Aminopeptidase P的切割作用形成。 | |||
T5652 |
L(+)-Leucinol
|
Aminopeptidase | Metabolism |
L(+)-Leucinol 是一种有效的亮氨酸氨基肽酶抑制剂。 | |||
T60021 |
ecMetAP-IN-1
|
Others | Others |
ecMetAP-IN-1 可用作 QSAR 模型,以使用多元线性回归研究蛋氨酸氨基肽酶抑制剂作为抗癌剂。 | |||
T64341 |
H-β-Ala-AMC TFA
|
Others | Others |
H-β-Ala-AMC TFA 是氨基肽酶的底物之一。 | |||
T18997 |
GPDA
Glycylproline p-nitroanilide tosylate,GPN |
Others | Others |
GPDA (Glycylproline p-nitroanilide tosylate) 是一种酶促反应检测底物,用于检测脯氨酰二肽氨基肽酶。 | |||
TP1917L1 |
Sar-[D-Phe8]-des-Arg9-Bradykinin acetate
Sar-[D-Phe8]-des-Arg9-Bradykinin acetate(126959-88-4 free base) |
Bradykinin Receptor | GPCR/G Protein |
Sar-[D-Phe8]-des-Arg9-Bradykinin acetate(126959-88-4 free base) 是一种有效的选择性缓激肽 B1 受体激动剂(兔主动脉中的 EC50 = 9.02 nM),对氨肽酶、激肽酶 I 和 II (ACE) 以及中性内肽酶切割具有抗性。在体内表现出降血压和血管生成活性。 | |||
T22255 | Amastatin | Others | Others |
Amastatin is a non-toxic inhibitor of aminopeptidase A and leucine aminopeptidase, and its Ki for aminopeptidase A is 1 µM . | |||
T24431 |
Matlystatin A
|
||
Matlystatin A is an inhibitor of aminopeptidase. It shows multiple inhibitory activities against both aminopeptidase N and matrix metalloproteinases. | |||
T25987 | Probestin | ||
Probestin is an aminopeptidase M inhibitor, isolated from Streptomyces azureus MH663-2F6. | |||
T32676 |
Leucylmethionine
Leu-met |
||
Leucylmethionine is a substrate for aminopeptidase M. | |||
T37062 |
L-Leucine-7-amido-4-methylcoumarin hydrochloride
|
||
L-Leu-AMC is a fluorogenic substrate for leucine aminopeptidase.1Upon enzymatic cleavage by leucine aminopeptidase, AMC is released and its fluorescence can be used to quantify leucine aminopeptidase activity. AMC displays excitation/emission maxima of 340-360/440-460 nm, respectively. 1.Izquierdo, M., Lin, D., O’Neill, S., et al.Development of a high-throughput screening assay to identify inhibitors of the major M17-leucyl aminopeptidase from Trypanosoma cruzi using rapidfire mass spectrometryS... | |||
T29485 | 7-Lysylalanyl-4-methylcoumarinamide | ||
7-Lysylalanyl-4-methylcoumarinamide is a Fluorogenic substrate for dipeptidyl aminopeptidase. | |||
T25940 |
Phebestin
|
||
Phebestin is an aminopeptidase N inhibitor, produced by Streptomyces sp. MJ716-m3. | |||
T15479 |
HFI-142
|
Others | Others |
HFI-142 is an inhibitor of insulin-regulated aminopeptidase (IRAP) (Ki: 2.01 μM). | |||
T25675 |
Leucinal
L-Leucinal |
||
Leucinal inhibits the activity of brain aminopeptidase and potentiates analgesia induced by leu-enkephalen. | |||
T28037 | Microginin 527 | ||
Microginin 527, a compound found in Microcystis, is an inhibitor of protein phosphatase, ACE, and leucine aminopeptidase. | |||
T68911 |
LAF-153
|
||
LAF-153 is a reversible Methionine Aminopeptidase‑2 (MetAP-2) Inhibitor. | |||
T19665 |
Amastatin hydrochloride
氨肽酶抑制剂盐酸盐,BIMI-1803,Amastatin HCl,ZX-AFC000547,ZXAFC000547,BIMI1803,J-000280,J000280 |
||
Amastatin HCl is an inhibitor of aminopeptidase. It also induces vasoconstriction. | |||
T78002 |
Spinorphin TFA
LVV-hemorphin-4 TFA |
||
Spinorphin TFA是一种脑啡肽降解酶抑制剂,能够抑制氨基肽酶、二肽基氨基肽酶III、血管紧张素转换酶以及脑非肽酶,常用于缓解疼痛研究中。 | |||
T26048 |
RB 101
RB101,RB-101 |
||
RB 101 suppresses enkephalinase and aminopeptidases; biologically cleaved at disulfide to produce inhibitors of both aminopeptidase N and neutral endopeptidase. | |||
T25897 |
OH-Ubenimex
p-Hydroxyubenimex,p-Hydroxybestatin |
||
OH-Ubenimex is an orally active aminopeptidase inhibitor that has an immunomodulating action. | |||
T13188 |
TP-004
|
Others | Others |
TP-004 is a potent and reversible methionine aminopeptidase 2 (MetAP2) inhibitor (IC50: 6 nM). | |||
T17110 |
TNP-470
AGM-1470 |
Others | Others |
TNP-470 is a methionine aminopeptidase-2 inhibitor. TNP-470 is also an angiogenesis inhibitor. | |||
T71626 |
Epibestatin Hydrochloride
|
||
Epibestatin Hydrochloride is a stabilizer of 14-3-3 PPIs, as well as a diastereoepimer of aminopeptidase inhibitor bestatin. | |||
T76589 |
H-Leu-Trp-Met-Arg-OH
|
||
H-Leu-Trp-Met-Arg-OH是一种四肽,可作为氨基肽酶(aminopeptidase)介导水解研究的底物。 | |||
T63915 | Sitagliptin fenilalanil | ||
Sitagliptin fenilalanil 是一种二肽氨基肽酶 (DPP-4)抑制剂。 | |||
T40839 |
H-Val-βNA
L-Valine β-naphthylamide,H-Val-βNA |
||
H-Val-βNA, also known as L-Valine β-naphthylamide, serves as a substrate for aminopeptidase and Valine arylamidase activities. | |||
T68605 | JNJ-4929821 | ||
JNJ-4929821 is a potent, reversible methionine aminopeptidase-2 (MetAP-2) inhibitor with IC50 of 8 nM. | |||
T20445 |
L-Leucine-p-nitroanilide
|
||
L-Leucine-p-nitroanilide is a substrate. It is used for the colorimetric determination of leucine aminopeptidase. | |||
T39488 | Relzomostat | ||
Relzomostat is a MetAP2 inhibitor, specifically targeting methionine aminopeptidase 2. It holds potential in research concerning obesity, type 2 diabetes, and other conditions associated with obesity. | |||
T25573 |
Ketomethylenebestatin
|
||
Ketomethylenebestatin is a carba-analog of bestatin,the aminopeptidase (AP) inhibitor. Ketomethylenebestatin is 10 fold less effective as an inhibitor of aminopeptidases than bestatin. | |||
T68382 |
Fumarranol
|
||
Fumarranol is an angiogenesis inhibitor. It also interacts with P. falciparum methionine aminopeptidase 2 to inhibit malaria parasite growth in vitro and in vivo. | |||
T11930 | M8891 | Others | Others |
M8891 is an orally active, reversible and brain penetrant Methionine Aminopeptidase-2 (MetAP-2) inhibitor(IC50 :54nM;Ki:4.33 nM).M8891 inhibits growth of primary endothelial cells as well as tumor cells and demonstrates antiangiogenic and antitumoral acti | |||
T76608 |
H-D-Ala-D-Ala-D-Ala-D-Ala-OH
|
||
H-Ala-D-Ala-D-Ala-D-Ala-OH 是 D-氨肽酶的底物。 | |||
T69346 |
A-357300
|
||
A-357300 is a potent, selective, reversible MetAP2 inhibitor with IC50 of 0.12 uM. Methionine aminopeptidase 2 inhibition is an effective treatment strategy for neuroblastoma in preclinical models. | |||
T61258 |
HFI-419
|
||
HFI-419 is a potent inhibitor of insulin-regulated aminopeptidase (IRAP) with a K i value of 0.48 μM. It is utilized in research pertaining to cognitive and memory impairments, including Alzheimer's disease, brain trauma, and stroke [1]. | |||
TP1771 |
NGR peptide Trifluoroacetate
|
||
NGR peptide Trifluoroacetate containing the asparagine-glycine-arginine (NGR) motif is recognized by CD13/aminopeptidase N (APN) receptor isoforms that are selectively overexpressed in tumor neovasculature. | |||
T82836 |
Bombinin
|
||
Bombinin为Bombina variegata所产生的抗菌肽,能够保护对氨基肽酶。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T1257 |
Bestatin
Ubenimex,乌苯美司 |
Others; Aminopeptidase; Antibacterial; Antibiotic; LTR | Immunology/Inflammation; Metabolism; Microbiology/Virology; Others |
Bestatin (Ubenimex) 是 CD13 (Aminopeptidase N)/APN 和 leukotriene A4 hydrolase 抑制剂,可用于癌症研究。 | |||
T7958 |
Methyl arachidate
花生酸甲酯,Methyl Icosanoate |
Others; Aminopeptidase | Metabolism; Others |
Methyl arachidate (Methyl Icosanoate) 是一种天然化合物,具有白三烯 A4 水解酶 (LTA4H) 抑制活性。 | |||
T3529 |
Bestatin hydrochloride
盐酸乌苯美司,Ubenimex hydrochloride,苯丁抑制素 |
Integrin; Aminopeptidase; Antibacterial; Antibiotic | Cytoskeletal Signaling; Metabolism; Microbiology/Virology |
Bestatin hydrochloride (Ubenimex hydrochloride) 是CD13(Aminopeptidase N)/APN 和leukotriene A4 hydrolase 抑制剂,可研究癌症。 | |||
T4755 |
2,3-Diaminopropanoic acid hydrochloride
DL-2,3-Diaminopropionic acid monohydroch,3-Amino-DL-alanine monohydrochloride,DL-2,3-二胺基丙酸盐酸盐 |
Others; Endogenous Metabolite | Metabolism; Others |
2,3-Diaminopropanoic acid hydrochloride (3-Amino-DL-alanine monohydrochloride) 是内源性代谢产物的一种。 | |||
T6841 |
Fumagillin
NSC9168,烟曲霉素,Amebacilin |
Others; HIV Protease; Antibiotic; Parasite | Microbiology/Virology; Others; Proteases/Proteasome |
Fumagillin (Amebacilin) 由烟曲霉菌中提取的一种抗菌药,有抗阿米巴活性。它通过抑制 HIV-1 viral protein R 活性来抑制 HIV‐1感染。 | |||
T2830 |
Betulinic acid
白桦脂酸,桦木酸,ALS-357,Lupatic acid,Betulic acid |
Apoptosis; Mitophagy; NF-κB; HIV Protease; Topoisomerase; Endogenous Metabolite; Aminopeptidase; Autophagy | Apoptosis; Autophagy; DNA Damage/DNA Repair; Metabolism; Microbiology/Virology; NF-κB; Proteases/Proteasome |
Betulinic acid (ALS-357) 是从白桦树皮中分离出来的一种五环三萜类天然产物,是真核细胞拓扑异构酶 I 的抑制剂,IC50值为 5 μM,具有抗逆转录病毒、抗疟疾、抗癌和抗炎特性。 | |||
T11203 | Enocyanin | Others | Others |
Enocyanin, an anthocyanin extracted from grapes, exhibits inhibitory effects on leucine aminopeptidase, acid phosphatase, γ-glutamyl transpeptidase, and esterase activity. | |||
T14121 |
Actinonin
(-)-Actinonin |
Aminopeptidase | Metabolism |
Actinonin ((-)-Actinonin) is a naturally occurring antibacterial agent produced by Actinomyces and a potent reversible peptide deformylase (PDF) inhibitor with a Ki of 0.28 nM, it also is an apoptosis inducer. Actinonin inhibits aminopeptidase M, aminopeptidase N and leucine aminopeptidase, it also inhibits MMP-1, MMP-3, MMP-8, MMP-9, and hmeprin α with Ki values of 300 nM, 1,700 nM, 190 nM, 330 nM, and 20 nM, respectively. Actinonin has antiproliferative and antitumor activities[1][2][3][4][5]. | |||
T62258 |
Bestatin trifluoroacetate
|
||
Bestatin trifluoroacetate (Ubenimex trifluoroacetate) 是一种 CD13 (Aminopeptidase N)/APN 和 leukotriene A4 hydrolase 抑制剂,经常用于研究癌症。 |