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Cat. No. | Product Name | Target | Signaling Pathways |
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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 。 | |||
T12284 |
O-Propargyl-Puromycin
OP-puro,O-Propargylpuromycin |
Others | Others |
O-Propargyl-Puromycin (OP-puro) 是一种高效的蛋白质合成抑制剂,是一种嘌呤霉素炔类似物。 | |||
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。 | |||
T25733 |
Lincophenicol
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Lincophenicol is an Escherichia coli ribosomal peptidyltransferase-catalyzed puromycin reaction inhibitor. | |||
T36338 |
AAF-CMK (trifluoroacetate salt)
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Tripeptidyl peptidase II (TPPII) is a serine peptidase of the subtilisin-type which removes tripeptides from the free NH2 terminus of oligopeptides. AAF-CMK is an irreversible inhibitor of TPPII commonly used at 10-100 μM. It does not significantly interfere with the chymotrypsin-like activity of the proteasome. AAF-CMK also inhibits bleomycin hydrolase and puromycin-sensitive aminopeptidase when used at 50 μM. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T19978 |
Puromycin
NSC 3055,NSC3055,Puromycine,嘌呤霉素,NSC-3055 |
Antibiotic | Microbiology/Virology |
Puromycin (NSC-3055) 是一种抗生素蛋白质合成抑制剂。它通过与 RNA 结合来抑制蛋白质合成。它还通过 Akt 磷酸化抑制食道癌细胞的生长和转移而用作抗癌药物。它是一种抗肿瘤剂和抗锥虫剂,在研究中用作蛋白质合成的抑制剂。 | |||
T2219 |
Puromycin dihydrochloride
CL13900 dihydrochloride,Puromycin 2HCl,嘌呤霉素二盐酸盐水合物,嘌呤霉素二盐酸盐 |
ribosome; DNA/RNA Synthesis; Antibacterial; Antibiotic | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
Puromycin dihydrochloride (CL13900 dihydrochloride) 属于肉桂酰胺腺苷抗生素,是一种蛋白质合成的抑制剂。Puromycin dihydrochloride 通过与 RNA 结合来抑制蛋白质合成,具有抗肿瘤和抗锥虫活性。 |