Actinonin
| 规格 | 价格 | 货期 | 数量 |
|---|---|---|---|
| 5mg | 请咨询 | 现货 | |
| 25mg | 请咨询 | 现货 |
特色产品
- 用于免疫印迹和质谱分析等后续操作
- 适用于30 KDa-130 KDa大小的蛋白
- 可将信号灵敏度提高100倍
- 同时保持稳定的特异性和分辨率
- 提供更高的转录效率并抑制免疫激活
- 使用5-moUTP和Cy5-utp修饰
产品描述
Actinonin is an antibiotic and CD13/aminopeptidase N (APN) inhibitor. Actinonin is a naturally occuring antibacterial agent produced by antinomycete with potent deformylase inhibitory effect [1].
In vitro: Actinonin showed an inhibitory effect in cell growth. The in vitro IC50 values of actinonin against NB4, HL6O human cell lines, AKR mouse leukemia cells CD13-negative cell lines RA.JI and DAUDI human lymphoma were about 2-5 μg/ml. Cell cycle analysis indicated that actinonin induced a G1 arrest in NB4 and HL6O cells. Intracellular flow cytometry showed that actinonin could induce cell apoptosis in 20-35% of the cells [2]. Actinonin dose-dependently inhibited the three forms (Zn-, Ni-, and Fe-) of peptide deformylases from both S. aureus and E. coli bacteria. The IC50 values of actinonin were 90, 3, 0.8, and 11 nM for Zn-PDF (E. coli), Ni-PDF (E. coli), Fe-PDF (E. coli), and Ni-PDF (S. aureus), respectively [2]. Actinonin is a tight binding inhibitor of E. coli Ni-PDF with a Ki of 0.3 nM [3].
In vivo: Actinonin showed dose-dependent antitumor effects on AKR leukemia, resulting in a survival advantage. In the syngeneic AKR mouse leukemia model, treatment with 100 p.g actinonin daily for 3 days beginning at day 3 after transplantation showed significant antitumor effects [2].
References:
[1]. Gordon J J, Kelly B K, Miller G A. Actinonin: an antibiotic substance produced by an actinomycete[J]. Nature, 1962, 195: 701-702.
[2]. Xu Y, Lai L T, Gabrilove J L, et al. Antitumor activity of actinonin in vitro and in vivo[J]. Clinical cancer research, 1998, 4(1): 171-176.
[3]. Chen D Z, Patel D V, Hackbarth C J, et al. Actinonin, a naturally occurring antibacterial agent, is a potent deformylase inhibitor[J]. Biochemistry, 2000, 39(6): 1256-1262.
产品性质
| 物理外观 | A solid |
| CAS号 | 13434-13-4 |
| 分子式 | C19H35N3O5 |
| 分子量 | 385.5 |
| 化学名称 | (2R)-N4-hydroxy-N1-[(1S)-1-[[(2S)-2-(hydroxymethyl)-1-pyrrolidinyl]carbonyl]-2-methylpropyl]-2-pentyl-butanediamide |
| 溶解度 | ≥50.2 mg/mL in DMSO; ≥51.1 mg/mL in EtOH; ≥4.56 mg/mL in H2O with ultrasonic |
| SMILES | CCCCC[C@H](CC(NO)=O)C(N[C@@H](C(C)C)C(N1[C@H](CO)CCC1)=O)=O |
| 存储条件 | -20°C |
| 运输条件 | 蓝冰 |
产品应用 (实验数据来自文献,APExBIO并未验证,仅供参考)
IC50和靶点
| 生物活性描述 | 放线菌素((-)-Actinonin)是一种由放线菌产生的天然抗菌剂。放线菌素能抑制氨肽酶 M、氨肽酶 N 和亮氨酸氨肽酶。放线菌素是一种强效的可逆肽变形酶(PDF)抑制剂,其 Ki 值为 0.28 nM。放线菌素还能抑制 MMP-1、MMP-3、MMP-8、MMP-9 和 hmeprin α,其 Ki 值分别为 300 nM、1,700 nM、190 nM、330 nM 和 20 nM。放线菌素是一种细胞凋亡诱导剂。放线菌素具有抗增殖和抗肿瘤活性。 |
生物相关数据
质量控制
APExBIO 顾客使用本产品发表的 1 篇科研文献
- 1. Chen Yingying, Xu Dingjie, et al. "Inhibition of miR-155-5p Exerts Anti-Fibrotic Effects in Silicotic Rats by Regulating Meprin α." EBioMedicine. 7 Aug 2019.



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