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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T18883 |
2-Di-1-ASP
|
Others | Others |
2-Di-1-ASP 是单苯乙烯基染料,对 G-四链体和双链 DNA 具有选择性。它普遍用作双链 DNA 的线粒体染色和凹槽结合荧光探针。 | |||
T4470 |
Pyridostatin TFA
|
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Pyridostatin TFA 是一种 G-四链体稳定剂,靶向原癌基因 Src,降低人乳腺癌细胞 SRC 蛋白水平和 SRC 依赖的细胞运动。它通过诱导复制和转录依赖的 DNA 损伤促进人类癌细胞生长停滞。 | |||
T60028 | MM41 | DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
MM41 是一种人类端粒和基因启动子 DNA 四链体稳定剂,对 MIA PaCa-2 胰腺癌细胞系的 IC50 <10 nM。 | |||
T13174 |
TMPyP4 tosylate
TMP 1363 |
DNA/RNA Synthesis; Telomerase | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
TMPyP4 tosylate (TMP 1363) 是四链体 (G-quadruplex) 的特异性配体,抑制四链体和 IGF-1 之间的相互作用。它也是端粒酶抑制剂,在骨肉瘤细胞系中显示抗肿瘤作用。 | |||
T7409 |
360A
3,3'-[2,6-吡啶二基二(羰基亚氨基)]二[1-甲基喹啉鎓] |
DNA/RNA Synthesis; Telomerase | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
360A 是一种稳定的G-四链体配体,还抑制 TRAP-G4 试验中端粒酶的端粒酶活性,IC50值为 300 nM。 | |||
T74613 | G-quadruplex DNA fluorescence probe 1 | ||
G-quadruplexDNA fluorescence probe 1 (Compound E1) 是一种选择性的G-quadruplexDNA 靶向荧光探针。G-quadruplexDNA fluorescence probe 1 能通过膜进入活细胞,具有低细胞毒性。 | |||
T1899 |
Pyridostatin
RR82,Pyridostatin Trifluoroacetate Salt |
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Pyridostatin (RR82) 是一种 G-四链体稳定剂,靶向原癌基因 Src,降低人乳腺癌细胞 SRC 蛋白水平和 SRC 依赖的细胞运动。它通过诱导复制和转录依赖的 DNA 损伤促进人类癌细胞生长停滞。 | |||
T26892 |
Braco-19
|
||
Braco-19 is a G-quadruplex ligand, it inhibits the growth of tumor. | |||
T13584 |
BMVC-8C3O
|
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
BMVC-8C3O 是一种 DNA G-四链体 (G4) 配体,可诱导人类端粒 DNA G4 中的非平行到平行形式的拓扑转换 | |||
T10352 |
APTO-253
LOR-253,LT-253 |
Apoptosis; c-Myc; KLF | Apoptosis; Cell Cycle/Checkpoint; MAPK |
APTO-253 (LOR-253) 抑制 c-Myc 表达,稳定 G-四链体 DNA,并诱导急性髓细胞白血病细胞的细胞周期停滞和凋亡。 它通过诱导 KLF4 肿瘤抑制因子介导抗癌活性,具有抗关节炎活性。 | |||
T16703 |
Quarfloxin
CX-3543 |
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Quarfloxin (CX-3543) 是一种氟喹诺酮衍生物,具有抗肿瘤活性,可靶向抑制RNA pol I 的活性,在神经母细胞瘤细胞中的 IC50 值在纳摩尔范围内。它破坏核糖体 DNA 模板中核仁蛋白和 G-四链体 DNA 结构之间的相互作用。 | |||
T10574 |
BMVC
|
Telomerase | DNA Damage/DNA Repair |
BMVC is a potent G-quadruplex (G4) stabilizer and a selective telomerase inhibitor (IC50: ~0.2 μM) with anticancer activities. BMVC inhibits Taq DNA polymerase (IC50: ~2.5 μM). | |||
T30745 |
Carboxy-pyridostatin
|
||
Carboxy-pyridostatin, as a fluorescent probe, can target G-quadruplex structures and trap cytoplasmic RNA G-quadruplex structures in cells. | |||
T32014 |
GTC365
GTC 365,NSC 177365,GTC-365,NSC-177365,NSC177365 |
||
GTC365 is an hTERT transcriptional repressor that acts in the early stages of the G-quadruplex folding pathway. | |||
T13504 |
360A iodide
360 A iodide |
Telomerase | DNA Damage/DNA Repair |
360A iodide is a selective stabilizer of G-quadruplex and inhibits telomerase activity (IC50: 300 nM in TRAP-G4 assay). | |||
T28942 |
Telomestatin
SOT 095,GM95,(R)-Telomestatin,GM 95,GM-95 |
||
Telomestatin is an inhibitor of the telomerase, it induces the formation of basket-type G-quadruplex (G4) structures from hybrid-type G-quadruplexes in the telomeric region. | |||
T13817 | Phen-DC3 | Others | Others |
Phen-DC3 is a G-quadruplex (G4) specific ligand which can inhibit FANCJ and DinG helicases (IC50s of 65±6 and 50±10 nM, respectively). | |||
T19212 |
BMVC2
o-BMVC |
Others | Others |
BMVC2 (o-BMVC), a carbazole derivative of BMVC, is a G-quadruplex (G4) stabilizer. | |||
T26872 |
BMVC4
BMVC 4,BMVC-4 |
||
BMVC4 is a G-quadruplex stabilizer. BMVC4 induces senescence by activation of pathways of response to DNA damage that was independent of its telomerase inhibitory activity. | |||
T33894 |
PBP2
PBP-2,PBP 2 |
||
PBP2 is a selective inducer of G-quadruplex structures from the unstructured single-stranded DNA conformations. PBP2 downregulates BCL-2 gene expression in cancer cells. | |||
T72572 |
Antitumor agent-85
|
||
Antitumor agent-85 是一种 G-quadruplex(G4) 配体,具有稳定不同 G4-DNA 结构的能力。Antitumor agent-85 具有高效的抗肿瘤特性。 | |||
T25255 |
CL67
CL-67,CL 67 |
||
CL67 is a hypoxia-inducible factor pathway inhibitor. It acts by binding to a G-quadruplex higher-order structure in the HIF promoter sequence in vitro. | |||
T72571 | Antitumor agent-84 | ||
Antitumor agent-84 是一种G-quadruplex(G4) 配体,具有稳定不同 G4-DNA 结构的能力。Antitumor agent-84 具有高效的抗肿瘤特性。 | |||
T13817L |
Phen-DC3 Trifluoromethanesulfonate
Phen-DC3 Triflate |
Others | Others |
Phen-DC3 Trifluoromethanesulfonate is a G-quadruplex (G4) specific ligand. It also can inhibit FANCJ and DinG helicases (IC50s: 65±6 and 50±10 nM, respectively). | |||
T74961 | Anticancer agent 84 | ||
Anticancer agent 84 是抗癌剂。Anticancer agent 84 通过稳定 G-四链体 (G4) 结构来抑制c-MYC 的转录。Anticancer agent 84 可用于癌症研究。 | |||
T37218 |
N-methyl Mesoporphyrin IX
|
||
N-methyl Mesoporphyrin IX 是广泛使用的 G-quadruplex DNA 特异性荧光结合剂,能有效监测 Aβ 纤颤。N-methyl Mesoporphyrin IX 对 G-四链体 DNA 敏感,对双链体、三链体和单链形式的 DNA 没有反应。N-methyl Mesoporphyrin IX 需通过与 Aβ 组装体堆叠才能发出强荧光。同时 N-methyl Mesoporphyrin IX 是一种原位抑制剂,是体外和细胞内 Aβ 淀粉样蛋白生成的非原位监测器。 | |||
T73264 | L2H2-6OTD | ||
L2H2-6OTD, 为含有一至四个G-四联体结合环的端粒抑制素类似物,显示出对端粒酶 (telomerase) 的抑制活性,其IC50值达到15 nM。 | |||
T72201 |
Pyridostatin hydrochloride
RR82 hydrochloride |
||
Pyridostatin (RR82) hydrochloride 是一种高选择性的 G-quadruplexDNA 稳定剂 (Kd=490 nM)。Pyridostatin hydrochloride 通过诱导复制和转录依赖的 DNA 损伤促进人类癌细胞生长停滞。Pyridostatin hydrochloride 靶向原癌基因 Src。Pyridostatin hydrochloride 降低人乳腺癌细胞 SRC 蛋白水平和 SRC 依赖的细胞运动。 | |||
T63765 | L5-DA | ||
L5-DA 是一种 G-四链体(G4)配体,能够选择性稳定 G4s。L5-DA 对 HeLa 细胞表现出明显的细胞毒性,其 IC50 值为 4.3 μM。L5-DA 能够稳定 HeLa 细胞中的 G4s,并可阻滞细胞周期及诱导细胞凋亡。 | |||
T74460 | c-Myc inhibitor 5 | ||
c-Myc inhibitor5 (DA3) 是一种荧光长链桥双嘌呤,可选择性靶向 c-MYCG-四链体(KD16 μM)。c-Myc inhibitor5 显示对 c-MYC 表达的抑制作用,而不是其他 G4 驱动的癌基因。 | |||
T74539 |
DIZ-3
|
||
DIZ-3为基于G4配体二聚化策略的选择性多聚体G4配体。该化合物通过插入G4-G4界面,稳定其高阶结构。通过诱导细胞周期停滞和细胞凋亡,DIZ-3在端粒(ALT)癌细胞的交替延长中抑制细胞增殖。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T5S2361 |
Epiberberine
|
ERK; Beta-Secretase; MEK; BACE; AMPK; AChR; AChE | Chromatin/Epigenetic; MAPK; Neuroscience; PI3K/Akt/mTOR signaling |
Epiberberine 是一种从黄连中得到的生物碱,是AChE 和BChE 抑制剂,和非竞争性BACE1抑制剂。在 3T3-L1 细胞分化早期,它能够下调 Raf/MEK1/2/ERK1/2 和 AMPKα/Akt 信号通路。它具有抗氧化作用,能够清除 ONOO-,可用于阿尔滋海默症和糖尿病的研究。 |