Fluensulfone

目录号: GC10705纯度: >98.50%同义词: 联氟砜,MCW-2
A nematicide

Fluensulfone
Cas No.: 318290-98-1
规格价格库存数量操作
1mg¥201.00现货
1
2mg¥296.00现货
1
5mg¥464.00现货
1
10mg¥763.00现货
1
25mg¥1,519.00现货
1
50mg¥2,217.00现货
1
100mg¥3,218.00现货
1

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产品描述 Description

Fluensulfone is identified as a new nematicide for chemical control of plant parasitic nematodes.

Plant parasitic nematodes can infest crops and present a threat to food security. Currently available chemical controls such as methyl bromide, organophosphates as well as carbamates have an unacceptable toxicity level to non-target organisms and are being withdrawn.

In vitro: Previous study showed that the model genetic organism Caenorhabditis elegans was susceptible to the treatment of fluensulfone. While the required dose was higher than that which had nematicidal activity against Meloidogyne spp. In addition, the profile of effects on motility, egg-hatching and survival was similar to that reported for plant parasitic nematodes.C. elegans therefore provided a tractable paradigm to analyze the effects of fluensulfone on nematode behaviour. Moreover, it was also found that fluensulfone had pleiotropic actions and inhibited development, egg-laying, egg-hatching, feeding and locomotion [1].

In vivo: In mice, but not in rats, fluensulfone at high doses has shown an increased incidence of lung adenomas. Moreover, fluensulfone was not genotoxic. In addition, the administration of fluensulfone to mice resulted in an early increase in Clara cell proliferation [2].

Clinical trial: Up to now, fluensulfone is still in the preclinical development stage.

References:
[1] Kearn J,Ludlow E,Dillon J,O'Connor V,Holden-Dye L.  Fluensulfone is a nematicide with a mode of action distinct from anticholinesterases and macrocyclic lactones. Pestic Biochem Physiol.2014 Feb;109:44-57.
[2] Strupp C,Banas DA,Cohen SM,Gordon EB,Jaeger M,Weber K.  Relationship of metabolism and cell proliferation to the mode of action of fluensulfone-induced mouse lung tumors: analysis of their human relevance using the IPCS framework. Toxicol Sci.2012 Jul;128(1):284-94.

实验参考方法 Experimental Reference Method

Cell experiment:

For these assays worms of different developmental stages are incubated in liquid with and without Fluensulfone for up to 24 h, and paralysis is scored. 400 μL of M9 phosphate buffer with either Fluensulfone (100 μM, 200 μM or 1 mM) or vehicle (0.5% acetone) is put into each well of a 24 well plate (5 replicates for each Fluensulfone concentration). 5 μL suspension of age synchronised C. elegans (L1, L2/3, L4 or one day old adult) is added to each well. Each well contains approximately 50 to100 worms. The number of worms not moving at 1, 2, 3, 4, 5, 6 and 24 h is determined. The experiment is conducted on two separate occasions with five replicates[1].

Animal experiment:

Groups of 10 female specific pathogen-free CD-1 mice each are treated with untreated diet, diet containing 1200 mg/kg Fluensulfone (high dose in carcinogenicity study), or 1305 mg/kg of isoniazid as a positive control substance for 3 or 7 days, respectively. Two and 14 h before sacrifice, the animals are injected ip with 100 μL of a 10 mg/mL aqueous bromodeoxyuridine (BrdU)-solution. Sacrifice by exsanguination under deep irreversible pentobarbital narcosis is performed early in the morning to assure that the animals are exposed to the test item until shortly before sacrifice[2].

References:

[1]. Kearn J, et al. Fluensulfone is a nematicide with a mode of action distinct from anticholinesterases and macrocyclic lactones. Pestic Biochem Physiol. 2014 Feb;109:44-57.
[2]. Strupp C, et al. Relationship of metabolism and cell proliferation to the mode of action of fluensulfone-induced mouse lung tumors: analysis of their human relevance using the IPCS framework. Toxicol Sci. 2012 Jul;128(1):284-94.

产品文档 Product Documents

Purity:>98.50%

化学性质Chemical Properties

CAS 号
318290-98-1
同义词
联氟砜,MCW-2
化学名
5-chloro-2-((3,4,4-trifluorobut-3-en-1-yl)sulfonyl)thiazole
SMILES
ClC1=CN=C(S(CC/C(F)=C(F)\F)(=O)=O)S1
分子式
C7H5ClF3NO2S2
分子量
291.7 g/mol
溶解性
≥ 29.2mg/mL in DMSO
保存条件
Store at -20°C
General tips
请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。
储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
为了提高溶解度,请将管子加热至 37°C,然后在超声波浴中震荡一段时间。
Shipping Condition
评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备 RT,或根据请求配备蓝冰。

计算工具摩尔浓度 / 稀释 / 分子量 / 单位换算 / 体内配方 / 溶解度

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