货号:A108674
同义名:
BAY2353; NSC 178296
Niclosamide can inhibit DNA replication and inhibit STAT3 with IC50 of 0.7 μM in a cell-free assay. Niclosamide selectively inhibits the phosphorylation of STAT3 and has no obvious inhibition against the activation of other homologues (e.g., STAT1 and STAT5). It is also an antiparasitic agent. It induced apoptosis by activating the intrinsic and caspase-independent pathway in human A549 and CL1-5 cells.
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产品名称 | Autophagy ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
SBI-0206965 |
+++
ULK1, IC50: 108 nM ULK2, IC50: 711 nM |
95% | |||||||||||||||||
Hydroxychloroquine sulfate | ✔ | 99% | |||||||||||||||||
Valproic acid sodium | ✔ | HDAC | 97% | ||||||||||||||||
PFK-015 |
++
PFKFB3, IC50: 207 nM |
99%+ | |||||||||||||||||
MRT68921 HCl |
++++
ULK1, IC50: 2.9 nM ULK2, IC50: 1.1 nM |
99%+ | |||||||||||||||||
ROC-325 | ✔ | 99%+ | |||||||||||||||||
Autophinib |
+++
Autophagy, IC50: 40 nM |
99% | |||||||||||||||||
Lys05 | ✔ | 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。 |
产品名称 | STAT1 ↓ ↑ | STAT3 ↓ ↑ | STAT5 ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Nifuroxazide | ✔ | 98% | |||||||||||||||||
Fludarabine | ✔ | 98% | |||||||||||||||||
Artesunate | ✔ | 98% | |||||||||||||||||
BP-1-102 |
+++
STAT3, Kd: 504 nM |
99%+ | |||||||||||||||||
Niclosamide |
++
STAT3, IC50: 0.7 μM |
98% | |||||||||||||||||
Napabucasin | ✔ | 98% | |||||||||||||||||
Cryptotanshinone |
++
STAT3, IC50: 4.6 μM |
98% | |||||||||||||||||
Stattic |
+
STAT3, IC50: 5.1 μM |
98% | |||||||||||||||||
NSC 74859 |
+
STAT3, IC50: 86 μM |
99%+ | |||||||||||||||||
Ochromycinone | ✔ | 98% | |||||||||||||||||
HO-3867 | ✔ | 97% | |||||||||||||||||
C188-9 |
++++
STAT3, Kd: 4.7 nM |
99%+ | |||||||||||||||||
HJC0152 | ✔ | 99% | |||||||||||||||||
SH5-07 | ✔ | 97% | |||||||||||||||||
SH-4-54 |
++++
STAT3, Kd: 300 nM |
+++
STAT5, Kd: 464 nM |
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。 |
靶点 |
|
描述 | Niclosamide (BAY2353) is an orally active antihelminthic agent primarily employed in research related to parasitic infections[1]. Niclosamide also functions as a potent STAT3 inhibitor, demonstrating an IC50 of 0.25 μM in HeLa cells[4]. Additionally, Niclosamide exhibits anticancer properties and can inhibit DNA replication in Vero E6 cells[2].[3].[5]. Niclosamide, produced under Good Manufacturing Practice (GMP) guidelines as Niclosamide, is used in parasitic infection research and also serves as an auxiliary reagent for cell therapy manufacturing[1]. This formulation maintains its potency as a STAT3 inhibitor with an IC50 of 0.25 µM in HeLa cells[4]. Niclosamide shows anti-cancer activities, including the inhibition of DNA replication in Vero E6 cells[2].[3].[5]. |
细胞系 | 浓度 | 检测类型 | 检测时间 | 活性说明 | 数据源 |
CHO cells | Function assay | Cytoprotective activity against anthrax fusion toxin FP59-induced cell death in CHO cells assessed as cell viability by MTT reduction assay | 19540764 | ||
HEK293 cells | Function assay | 8 h | Inhibition of Wnt/beta-catenin in HEK293 cells assessed as inhibition of Wnt3A-stimulated TOPFlash activity after 8 hrs, IC50=0.34 μM | 26272032 | |
HEK293 cells | Function assay | 8 h | Inhibition of Wnt3A/beta-casein signaling in HEK293 cells after 8 hrs by TOPflash reporter assay, IC50=0.4 μM | 23453073 | |
human A431 cells | Proliferation assay | 72 h | Antiproliferative activity against human A431 cells after 72 hrs by MTT assay, IC50=8.8 μM | 24900231 | |
Animal study | In vivo, Niclosamide administered via oral gavage at doses of 100 mg/kg and 200 mg/kg once a week over eight weeks, significantly reduces tumor growth in models of adrenocortical carcinoma[3].The same dosage and administration schedule for Niclosamide (100 mg/kg, 200 mg/kg; oral gavage; once a week; 8 weeks) is used to inhibit tumor growth in adrenocortical carcinoma in vivo, confirming its therapeutic potential across different formulations and applications[3]. |
NCT号 | 适应症或疾病 | 临床期 | 招募状态 | 预计完成时间 | 地点 |
NCT01296958 | Taenia Solium Taeniasis | Not Applicable | Completed | - | Peru ... 展开 >> San Marcos University Lima, Peru 收起 << |
NCT01189903 | Asian Colorectal Cancer Patien... 展开 >>ts 收起 << | Phase 2 Phase 3 | Unknown | - | Singapore ... 展开 >> National University Hospital Singapore, Singapore, 119074 收起 << |
NCT00138359 | Intestinal Parasitism | Not Applicable | Terminated | - | Peru ... 展开 >> Universidad Peruana Cayetano Heredia Lima, Peru 收起 << |
计算器 | ||||
存储液制备 | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
3.06mL 0.61mL 0.31mL |
15.28mL 3.06mL 1.53mL |
30.57mL 6.11mL 3.06mL |
CAS号 | 50-65-7 |
分子式 | C13H8Cl2N2O4 |
分子量 | 327.12 |
SMILES Code | O=C(NC1=CC=C([N+]([O-])=O)C=C1Cl)C2=CC(Cl)=CC=C2O |
MDL No. | MFCD00057597 |
别名 | BAY2353; NSC 178296; Clonitralide, Fenasal, BAY 2353, BAY-2353, BAY2353, NSC 178296, NSC178296, NSC-178296, WR-46234, WR46234, WR 46234,; Niclocide |
运输 | 蓝冰 |
InChI Key | RJMUSRYZPJIFPJ-UHFFFAOYSA-N |
Pubchem ID | 4477 |
存储条件 |
In solvent -20°C:3-6个月-80°C:12个月 Pure form Sealed in dry, room temperature |