货号:A810672
同义名:
ICI 69653; NSC 234714
Aphidicolin是一种 DNA 聚合酶 α 和 δ 的抑制剂,通过抑制 DNA 合成来阻止细胞有丝分裂。Aphidicolin 来源于 Cephalosporium aphidicola,具有抗病毒和增强阿拉伯糖基核苷诱导细胞凋亡的作用,广泛用于抗癌及抗病毒研究。


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|---|---|---|---|---|---|---|---|
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| 产品名称 | DNA synthesis ↓ ↑ | helicase ↓ ↑ | RdRp ↓ ↑ | ribonucleotide reductase ↓ ↑ | tRNA synthetase ↓ ↑ | YB-1 ↓ ↑ | 其他靶点 | 纯度 | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Fexinidazole | ✔ | 98% | |||||||||||||||||
| Daptomycin | ✔ | 98% | |||||||||||||||||
| Blasticidin S·HCl | ✔ | 98% | |||||||||||||||||
| Metronidazole | ✔ | 98% | |||||||||||||||||
| Daunorubicin HCl |
+++
DNA synthesis, Ki: 20 nM |
98% | |||||||||||||||||
| Triglycidyl isocyanurate | ✔ | p53 | 98+% | ||||||||||||||||
| Nedaplatin | ✔ | 99%+ | |||||||||||||||||
| Oxolinic acid | ✔ | 98+% | |||||||||||||||||
| Bendamustine | ✔ | 98+% | |||||||||||||||||
| Trifluridine | ✔ | 98% | |||||||||||||||||
| Robinetin | ✔ | 99%+ | |||||||||||||||||
| Carboplatin | ✔ | 99% | |||||||||||||||||
| Cidofovir | ✔ | 99% | |||||||||||||||||
| Cisplatin | ✔ | 99% | |||||||||||||||||
| Cytarabine |
++++
DNA synthesis, IC50: 16 nM |
98% | |||||||||||||||||
| Acelarin |
++++
DNA synthesis, EC50: 0.2 nM |
99%+ | |||||||||||||||||
| Oxaliplatin | ✔ | 98% | |||||||||||||||||
| YK-4-279 | ✔ | 99%+ | |||||||||||||||||
| ML216 |
+
BLMfull-length, IC50: 2.98 μM BLM636-1298, IC50: 0.97 μM |
99%+ | |||||||||||||||||
| RK-33 | ✔ | 98% | |||||||||||||||||
| Brr2-IN-3 | ✔ | 99%+ | |||||||||||||||||
| Phen-DC3 Trifluoromethanesulfonate | ✔ | 95% | |||||||||||||||||
| Favipiravir | ✔ | 99% | |||||||||||||||||
| Suramin sodium salt |
++
RdRp, IC50: 0.26 μM |
99%+ | |||||||||||||||||
| Clofarabine |
++
Ribonucleotide reductase, IC50: 65 nM |
97% | |||||||||||||||||
| Didox | ✔ | 98% | |||||||||||||||||
| (E)-3-AP | ✔ | 99% | |||||||||||||||||
| Halofuginone |
+++
prolyl-tRNA synthetase, Ki: 18.3nM |
99%+ | |||||||||||||||||
| BC-LI-0186 |
+++
Leucyl-tRNA synthetase, IC50: 46.11 nM Leucyl-tRNA synthetase, Kd: 42.1 nM |
98% | |||||||||||||||||
| SU056 |
+
YB-1, IC50: 1.73 μM |
98% | |||||||||||||||||
| 1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 | |||||||||||||||||||
| Concentration | Treated Time | Description | References | |
| U2OS cells | 5 μg/ml | 3 hours | Detect S746-phosphorylation of Exo1 under replication stress | Mol Cell. 2019 Jun 20;74(6):1123-1137. e6 |
| Human cell extract | 100–200 μM | 60 min | Inhibition of cccDNA formation | Nat Microbiol. 2020 May;5(5):715-726 |
| U2OS cells | 0.5 μM | 4 h | To investigate the effect of Aphidicolin on ionizing radiation-induced γH2AX foci formation, results showed that APH reduced the proportion of γH2AX-positive cells. | Nucleic Acids Res. 2012 Aug;40(14):6585-94 |
| AA8 cells | 0.5 μM | 4 h | To study the effect of Aphidicolin on ionizing radiation-induced RAD51 foci formation, results showed that APH significantly decreased the proportion of RAD51-positive cells. | Nucleic Acids Res. 2012 Aug;40(14):6585-94 |
| SPD8 cells | 0.5 μM | 4 h | To investigate the effect of Aphidicolin on ionizing radiation-induced homologous recombination repair, results showed that APH significantly reduced IR-induced recombination frequencies. | Nucleic Acids Res. 2012 Aug;40(14):6585-94 |
| embryonic mouse submandibular gland cells | 500 ng/ml | 24 h | Aphidicolin inhibited the growth of embryonic submandibular glands by interfering with DNA replication, with effects comparable to Barasertib | Cell Death Discov. 2021 Jan 18;7(1):16 |
| DT40 cells | 5 μM | 1 hour | Inhibits DNA polymerase activity, reduces collision between replication forks and Top1-cc, thereby decreasing CPT sensitivity and Top1 degradation | J Biol Chem. 2014 Apr 18;289(16):11374-11384 |
| Chinese hamster lung fibroblast cell line GMA32 | 0.3, 0.5 and 0.8 µg/ml | 20.5 h | To evaluate the effect of Aphidicolin on chromosome breaks, results showed that Aphidicolin induced chromosome breaks in the GNAI3–GNAT2 region | Nucleic Acids Res. 2000 Dec 1;28(23):4805-13 |
| HPV31 and HPV18 cells | 4 μM | 48 h | To study the effect of Aphidicolin on different HPV genotypes, results showed that Aphidicolin significantly reduced viral genome copy numbers of HPV31 and HPV18. | J Virol. 2013 Apr;87(7):3979-89 |
| W12E cells | 4 μM | 48 h | To study the effect of Aphidicolin on the stability of HPV16, HPV18, and HPV31 viral genomes, results showed that Aphidicolin significantly reduced viral genome copy numbers. | J Virol. 2013 Apr;87(7):3979-89 |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
2.95mL 0.59mL 0.30mL |
14.77mL 2.95mL 1.48mL |
29.54mL 5.91mL 2.95mL |
|
| CAS号 | 38966-21-1 |
| 分子式 | C20H34O4 |
| 分子量 | 338.48 |
| SMILES Code | C[C@@]12[C@]34[C@](CC[C@@]1([H])[C@@](C)([C@@H](CC2)O)CO)([H])C[C@@H]([C@](O)(CC4)CO)C3 |
| MDL No. | MFCD00083214 |
| 别名 | ICI 69653; NSC 234714; (+)-Aphidicolin |
| 运输 | 蓝冰 |
| 存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Sealed in dry, 2-8°C |
| 溶解方案 |
DMSO: 50 mg/mL(147.72 mM),配合低频超声,并水浴加热至45℃助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO 以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
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