
Indolactam V
CAS No. 90365-57-4
Indolactam V ( -)-Indolactam V )
产品货号. M16498 CAS No. 90365-57-4
Indolactam V ((-)-Indolactam V) 是一种吲哚生物碱肿瘤促进剂,可激活蛋白激酶 C (PKC)。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥4836 | 有现货 |
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50MG | ¥18954 | 有现货 |
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100MG | ¥28674 | 有现货 |
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200MG | 获取报价 | 有现货 |
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500MG | 获取报价 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称Indolactam V
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述Indolactam V ((-)-Indolactam V) 是一种吲哚生物碱肿瘤促进剂,可激活蛋白激酶 C (PKC)。
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产品描述Indolactam V ((-)-Indolactam V) is an indole alkaloid tumor promoter that activates protein kinase C (PKC), binds to PKC regulatory domains of mouse skin PKCη and rat brain PKCγ with Ki values of 3.4 nM and 1 uM, respectively; induces differentiation of human embryonic stem cells into pancreatic progenitors through activation of PKC signaling.
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体外实验(-)-Indolactam V is a PKC activator, with Kis of 3.36 nM, 1.03 μM for η-CRD2 (PKCη surrogate peptide), γ-CRD2 (PKCγ surrogate peptide), and has antitumor activity. (-)-Indolactam V shows Kds of 5.5 nM (η-C1B), 7.7 nM (ε-C1B), 8.3 nM (δ-C1B), 18.9 nM (β-C1A-long), 20.8 nM (α-C1A-long), 137 nM (β-C1B), 138 nM (γ-C1A), 213 nM (γ-C1B), respectively. (-)-Indolactam V (20 nM-5 μM) dose-dependently affects multiple hESC lines, such as HUES 2, 4 and 8. (-)-Indolactam V also increases the mRNA levels of Pdx1, HNF6, PTF1A, SOX9, HB9 and PROX1. In addition, (-)-Indolactam V (300 nM) functions in both mouse and human cells and confirms that some signals for pancreatic development.
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体内实验——
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同义词-)-Indolactam V
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通路Angiogenesis
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靶点PKC
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受体PKC
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研究领域Inflammation/Immunology
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适应症——
化学信息
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CAS Number90365-57-4
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分子量301.3834
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分子式C17H23N3O2
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纯度>98% (HPLC)
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溶解度10 mM in DMSO
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SMILESO=C(N[C@H](CO)C1)[C@H](C(C)C)N(C)C2=CC=CC3=C2C1=CN3
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化学全称3H-Pyrrolo[4,3,2-gh]-1,4-benzodiazonin-3-one, 1,2,4,5,6,8-hexahydro-5-(hydroxymethyl)-1-methyl-2-(1-methylethyl)-, (2S,5S)-
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Masuda A, et al. Biosci Biotechnol Biochem. 2002 Jul;66(7):1615-7.
2. Heikkil? J, et al. Biochem Biophys Res Commun. 1989 Aug 15;162(3):1207-13.
3. Chen S, et al. Nat Chem Biol. 2009 Apr;5(4):258-65.
4. Kazanietz MG, et al. Mol Pharmacol. 1993 Aug;44(2):298-307.
产品手册




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