货号:A724668
同义名:
AQ4N dihydrochloride; Banoxantrone dihydrochloride
Banoxantrone dihydrochloride是一种新型生物还原剂,可以还原为稳定的 DNA 亲和化合物 AQ4。AQ4 是一种有效的拓扑异构酶 II 抑制剂。
HazMat Fee + There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.
| Type | HazMat fee for 500 gram (Estimated) |
| Excepted Quantity | USD 0.00 |
| Limited Quantity | USD 15-60 |
| Inaccessible (Haz class 6.1), Domestic | USD 80+ |
| Inaccessible (Haz class 6.1), International | USD 150+ |
| Accessible (Haz class 3, 4, 5 or 8), Domestic | USD 100+ |
| Accessible (Haz class 3, 4, 5 or 8), International | USD 200+ |


| 规格 | 价格 | 会员价 | 库存 | 数量 | |||
|---|---|---|---|---|---|---|---|
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| 产品名称 | Topo I ↓ ↑ | Topo II ↓ ↑ | Topo IV ↓ ↑ | Topoisomerase ↓ ↑ | 其他靶点 | 纯度 | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Ellagic acid | ✔ | 98% | |||||||||||||||||
| β-Lapachone | ✔ | 99%+ | |||||||||||||||||
| (s)-10-hydroxycamptothecin | ✔ | 98+% | |||||||||||||||||
| Camptothecin |
++
Topo I, IC50: 0.68 μM |
98% | |||||||||||||||||
| Betulinic acid |
++
Eukaryotic topoisomerase I, IC50: 5 μM |
98% | |||||||||||||||||
| Topotecan |
++++
Topo I (MCF-7 Luc cells), IC50: 13 nM Topo I (DU-145 Luc cells), IC50: 2 nM |
98% | |||||||||||||||||
| Irinotecan HCl Trihydrate | ✔ | 98% | |||||||||||||||||
| SN-38 | ✔ | 98% | |||||||||||||||||
| Levofloxacin hydrate | ✔ | 98% | |||||||||||||||||
| Dexrazoxane | ✔ | 99%+ | |||||||||||||||||
| Ofloxacin | ✔ | 98+% | |||||||||||||||||
| Enoxacin | ✔ | 99%+ | |||||||||||||||||
| Flumequine |
+
Topo II, IC50: 15 μM |
98% | |||||||||||||||||
| Levofloxacin | ✔ | 97% | |||||||||||||||||
| Etoposide | ✔ | 98% | |||||||||||||||||
| Pefloxacin mesylate dihydrate | ✔ | 99.5% | |||||||||||||||||
| Marbofloxacin | ✔ | 98+% | |||||||||||||||||
| Voreloxin HCl | ✔ | 98% | |||||||||||||||||
| Mitoxantrone 2HCl | ✔ | PKC | 98% | ||||||||||||||||
| Nalidixic acid | ✔ | 98% | |||||||||||||||||
| Doxorubicin | ✔ | 97% | |||||||||||||||||
| Novobiocin sodium | ✔ | 95% | |||||||||||||||||
| Amonafide | ✔ | 99%+ | |||||||||||||||||
| Pirarubicin | ✔ | 98%+ | |||||||||||||||||
| Idarubicin HCl |
+++
Topo II (MCF-7 cells), IC50: 3.3 ng/mL |
99%+ | |||||||||||||||||
| Genistein | ✔ | EGFR | 98% | ||||||||||||||||
| Teniposide | ✔ | 98% | |||||||||||||||||
| Moxifloxacin | ✔ | 98% | |||||||||||||||||
| Ciprofloxacin | ✔ | 98% | |||||||||||||||||
| Clinafloxacin | ✔ | 99% | |||||||||||||||||
| Gatifloxacin | ✔ | 98% | |||||||||||||||||
| Daunorubicin HCl |
+++
DNA synthesis, Ki: 20 nM |
98% | |||||||||||||||||
| Epirubicin HCl | ✔ | 99%+ | |||||||||||||||||
| 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 | |
| U87MG cells | 100 μM | 48 h | Evaluate the loading efficiency and subsequent release capability of AQ4N in M1 macrophages | Signal Transduct Target Ther. 2022 Mar 16;7(1):74 |
| Administration | Dosage | Frequency | Description | References | ||
| Mice | T50/80 mammary carcinoma model | Intraperitoneal injection | 50–100 mg/kg | Single dose | To evaluate the ability of AQ4N to potentiate the anti-tumour effect of cisplatin, results showed that AQ4N significantly enhanced the anti-tumour effect of cisplatin | Br J Cancer. 2001 Aug 17;85(4):625-9 |
| B6D2F1 mice | T50/80 mammary carcinoma model | Intraperitoneal injection | 20-320 mg/kg (oxic), 3-130 mg/kg (hypoxic) | Single dose | To evaluate the anti-tumour effect of AQ4N under hypoxic conditions, showing a dose enhancement ratio (DER) of 5.1, indicating reduction to AQ4 in vivo and enhanced anti-tumour toxicity. | Br J Cancer. 1995 Jul;72(1):76-81 |
| Mice | MAC16, MAC26, RIF-1, NT and SCCVII tumor models | Intraperitoneal injection | 200–250 mg/kg | Single dose | To evaluate the anti-tumor effects of AQ4N as a single agent or in combination with radiotherapy and chemotherapy. Results showed that AQ4N was effective as a single agent in MAC16 tumors, and significantly enhanced anti-tumor effects when combined with radiotherapy or chemotherapy in other tumor models. | Br J Cancer. 2000 Jun;82(12):1984-90 |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
1.93mL 0.39mL 0.19mL |
9.66mL 1.93mL 0.97mL |
19.33mL 3.87mL 1.93mL |
|
| CAS号 | 252979-56-9 |
| 分子式 | C22H30Cl2N4O6 |
| 分子量 | 517.4 |
| SMILES Code | O=C(C1=C2C(O)=CC=C1O)C3=C(NCC[N+](C)([O-])C)C=CC(NCC[N+](C)([O-])C)=C3C2=O.[H]Cl.[H]Cl |
| MDL No. | MFCD19690955 |
| 别名 | AQ4N dihydrochloride; Banoxantrone dihydrochloride |
| 运输 | 蓝冰 |
| InChI Key | SBWCPHUXRZRTDP-UHFFFAOYSA-N |
| Pubchem ID | 72941779 |
| 存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Inert atmosphere, 2-8°C |
| 溶解方案 |
DMSO: 25 mg/mL(48.32 mM),配合低频超声助溶,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 H2O: 20 mg/mL(38.65 mM),配合低频超声助溶 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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