产品名称
PhenDC3, ≥97% (HPLC)
InChI
1S/C34H24N6O2.2CHF3O3S/c1-39-19-25(17-23-7-3-5-9-29(23)39)35-33(41)27-15-13-21-11-12-22-14-16-28(38-32(22)31(21)37-27)34(42)36-26-18-24-8-4-6-10-30(24)40(2)20-26;2*2-1(3,4)8(5,6)7/h3-20H,1-2H3;2*(H,5,6,7)
InChI key
PYJCATLYPXPYHF-UHFFFAOYSA-N
SMILES string
O=C(NC1=CC2=CC=CC=C2[N+](C)=C1)C3=CC=C4C=CC5=CC=C(N=C5C4=N3)C(NC6=CC7=CC=CC=C7[N+](C)=C6)=O.O=S([O-])(C(F)(F)F)=O.O=S([O-])(C(F)(F)F)=O
assay
≥97% (HPLC)
form
powder
color
white to beige
solubility
DMSO: 2 mg/mL, clear
storage temp.
2-8°C
相关类别
Application
PhenDC3 已被用于:
- 作为四链体(G4) 配体,研究其对 RNA 四链体(rG4) 与核仁素(NCL) 结合的影响
- 作为 DNA/RNA G-四链体(GQs) 配体研究其对双同源框 4(DUX4) 基因表达的影响
- 作为 G4 配体,通过荧光共振能量转移(FRET) 熔解法研究其对 pre-miR-92b rG4 复合物和双链 DNA 的稳定性和选择性
Biochem/physiol Actions
PhenDC3(Phen-DC3)是一种双喹啉衍生的菲咯啉-二甲酰胺,它以高亲和力靶向 DNA 和 RNA G-四链体(G4)结构(DNA DC50 在 μM = 0.31/22AG K+,0.25/22AG Na+,0.30/TBA; RNA DC50 in μM = 0.11/(G3U)3G3,0.12/(G3U2)3G3, 0.16/(G3U3)3G3)和选择性(双链 DNA DC50 >2.5 μM)。PhenDC3 在基于细胞的报告基因检测(0.1-10 μM)中抑制具有 5′UTR G4 结构的报告基因 mRNA 构建体的翻译,但不抑制那些没有的翻译,并通过在延伸过程中促进端粒酶与其产物的解离来降低端粒酶的持续合成能力。NMR 分析表明,PhenDC3 通过与顶部 G-四重奏的鸟嘌呤碱基的广泛堆叠与四链体相互作用。一个强大的基准工具,用于探测和阐明细胞 DNA 和 RNA G4 结构的生物学作用。
高亲和力 DNA 和 RNA G-四链体(G4)稳定配体。探测细胞 DNA 和 RNA G4 功能的基准工具。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Judith Lopes et al.
The EMBO journal, 30(19), 4033-4046 (2011-08-30)
G-quadruplexes are four-stranded nucleic acid structures whose biological functions remain poorly understood. In the yeast S. cerevisiae, we report that G-quadruplexes form and, if not properly processed, pose a specific challenge to replication. We show that the G-quadruplex-prone CEB1 tandem
Efficient suppression of gene expression by targeting 5'-UTR-based RNA quadruplexes with bisquinolinium compounds.
Kangkan Halder et al.
Chembiochem : a European journal of chemical biology, 12(11), 1663-1668 (2011-06-18)
Kevin Kok-Phen Yan et al.
Nucleic acids research, 49(14), 8339-8354 (2021-07-25)
The identification of G-quadruplex (G4) binding proteins and insights into their mechanism of action are important for understanding the regulatory functions of G4 structures. Here, we performed an unbiased affinity-purification assay coupled with mass spectrometry and identified 30 putative G4
Tiago Santos et al.
Biochemical pharmacology, 189, 114208-114208 (2020-08-30)
The development of novel biomarkers for early-stage diagnosis of prostate cancer (PCa) has attracted the attention of researchers in the last decade. Nucleolin (NCL) has emerged as a possible biomarker of PCa due to its high expression levels in the
Tovah A Day et al.
Nature communications, 8, 15110-15110 (2017-04-28)
Chromosomal rearrangements are essential events in the pathogenesis of both malignant and nonmalignant disorders, yet the factors affecting their formation are incompletely understood. Here we develop a zinc-finger nuclease translocation reporter and screen for factors that modulate rearrangements in human
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