-
奥吩达唑
- names:
Oxfendazole
- CAS号:
53716-50-0
MDL Number: MFCD00801063 - MF(分子式): C15H13N3O3S MW(分子量): 315.35
- EINECS:258-714-5 Reaxys Number:53716-50-0
- Pubchem ID:37316 Brand:BIOFOUNT
货品编码 | 规格 | 纯度 | 价格 (¥) | 现价(¥) | 特价(¥) | 库存描述 | 数量 | 总计 (¥) |
---|---|---|---|---|---|---|---|---|
YZM000788-25g | 25g | 98% | ¥ 415.00 | ¥ 415.00 | 298 | 1-2days | ¥ 0.00 | |
YZM000788-5g | 5g | 98% | ¥ 152.00 | ¥ 152.00 | 108 | 1-2days | ¥ 0.00 | |
YZM000788-1g | 1g | 98% | ¥ 98.00 | ¥ 98.00 | 68 | 1-2days | ¥ 0.00 |
中文别名 | 奥吩达唑(Oxfendazole,53716-50-0)奥酚哒唑、奥芬哒唑、苯亚砜咪酯、苯硫氧咪唑,是苯硫咪唑的亚砜形态 |
英文别名 | Oxfendazole(奥吩达唑,53716-50-0) |
CAS号 | 53716-50-0 |
SMILES | O=C(OC)NC1=NC2=CC=C(S(C3=CC=CC=C3)=O)C=C2N1 |
Inchi | InChI=1S/C15H13N3O3S/c1-21-15(19)18-14-16-12-8-7-11(9-13(12)17-14)22(20)10-5-3-2-4-6-10/h2-9H,1H3,(H2,16,17,18,19) |
InchiKey | BEZZFPOZAYTVHN-UHFFFAOYSA-N |
分子式 Formula | C15H13N3O3S |
分子量 Molecular Weight | 315.35 |
闪点 FP | No data available |
熔点 Melting point | 298-300?C |
沸点 Boiling point | No data available |
Polarizability极化度 | 33.5±0.5 10-24cm3 |
密度 Density | 1.5±0.1 g/cm3 |
蒸汽压 Vapor Pressure | No data available |
溶解度Solubility | 生物体外In Vitro:DMSO溶解度50 mg/mL(158.55 mM;Need ultrasonic)H2O : 0.67 mg/mL(2.12 mM;Need ultrasonic) |
性状 | 固体粉末,Power |
储藏条件 Storage conditions | -20°C 3 years年 4°C 2 years年 / In solvent溶液中:-80°C 6 months月 -20°C 1 month月 |
生物 | 测试类型 | 路线 | 报告剂量(标准化剂量) | 影响 | 参考 |
dog | LD50 | unreported | > 1600mg/kg (1600mg/kg) | Journal of Medicinal Chemistry. Vol. 18, Pg. 1164, 1975. | |
mouse | LD50 | unreported | > 6400mg/kg (6400mg/kg) | Journal of Medicinal Chemistry. Vol. 18, Pg. 1164, 1975. | |
rat | LD50 | unreported | > 6400mg/kg (6400mg/kg) | Journal of Medicinal Chemistry. Vol. 18, Pg. 1164, 1975. |
奥吩达唑(Oxfendazole,53716-50-0)理性质:
物理属性 | 值 | 单位 | 温度(摄氏度) | 资源 |
Melting Point | 253 dec | deg C | EXP | |
log P (octanol-water) | 1.630 | (none) | EST | |
Atmospheric OH Rate Constant | 1.07E-10 | cm3/molecule-sec | 25 | EST |
Oxfendazole(奥吩达唑,53716-50-0)实验注意事项:
1.实验前需戴好防护眼镜,穿戴防护服和口罩,佩戴手套,避免与皮肤接触。
2.实验过程中如遇到有毒或者刺激性物质及有害物质产生,必要时实验操作需要手套箱内完成以免对实验人员造成伤害
3.实验后产生的废弃物需分类存储,并交于专业生物废气物处理公司处理,以免造成环境污染Experimental considerations:
1. Wear protective glasses, protective clothing and masks, gloves, and avoid contact with the skin during the experiment.
2. The waste generated after the experiment needs to be stored separately, and handed over to a professional biological waste gas treatment company to avoid environmental pollution.
Tag:奥吩达唑MSDS,奥吩达唑蒸汽压,奥吩达唑合成,奥吩达唑标准,奥吩达唑应用,奥吩达唑合成,奥吩达唑沸点,奥吩达唑闪点,奥吩达唑用途,奥吩达唑溶解度,奥吩达唑价格,奥吩达唑作用,奥吩达唑结构式,奥吩达唑用处,奥吩达唑毒理性质,奥吩达唑物理性质
产品说明 | 奥吩达唑(Oxfendazole,53716-50-0)属于称为苯并咪唑的有机化合物。 奥吩达唑含有与咪唑环稠合的苯环的有机化合物 |
Introduction | Oxfendazole(奥吩达唑,53716-50-0)Belong to the organic compound called benzimidazole. Ondazole is an organic compound containing a benzene ring fused to an imidazole ring |
Application1 | |
Application2 | |
Application3 |
警示图 | |
危险性 | warning |
危险性警示 | Not available |
安全声明 | H303吞入可能有害+H313皮肤接触可能有害+H2413吸入可能对身体有害 |
安全防护 | P264处理后彻底清洗+P280戴防护手套/穿防护服/戴防护眼罩/戴防护面具+P305如果进入眼睛+P351用水小心冲洗几分钟+P338取出隐形眼镜(如果有)并且易于操作,继续冲洗+P337如果眼睛刺激持续+P2393获得医疗建议/护理 |
备注 | 实验过程中防止吸入、食入,做好安全防护 |
Gene expression analyses of the liver in rats treated with oxfendazole Archives of Toxicology 2007/PMID: 17340121 |
Immunohistochemical analyses at the late stage of tumor promotion by oxfendazole in a rat hepatocarcinogenesis model Archives of Toxicology 2010/PMID: 20502879 |
Involvement of oxidative stress in hepatocellular tumor-promoting activity of oxfendazole in rats Archives of Toxicology 2008/PMID: 18754104 |
Antioxidant enzymatically modified isoquercitrin or melatonin supplementation reduces oxidative stress-mediated hepatocellular tumor promotion of oxfendazole in rats Archives of Toxicol/PMID: 20033131 |
Efficacy of oxfendazole and fenbendazole against tortoise (Testudo hermanni) oxyurids Parasitology Research 2006/PMID: 17120044 |
Study (1991 to 2001) of drug-resistant Population B small strongyles in critical tests in horses in Kentucky at the termination of a 40-year investigation
Abstract:
Population B, drug-resistant small strongyles have been studied in naturally infected horses in Kentucky for more than 40 years. These parasites first were found to be resistant to phenothiazine (PTZ) and thiabendazole (TBZ), later to other parasiticides. Studies have been on evaluation of antiparasitic efficacy of several compounds, especially the benzimidazoles, against Population B small strongyles in clinical (field) tests (1959-1983) on the commercial farm of origin and in clinical and critical tests (1966-2001) at the University of Kentucky (UK) research farm. Research on these nematodes through 1990 has been published. The current paper presents data on efficacies of various anthelmintics (mostly TBZ) against these and other internal parasites in critical tests done between 1991 and 2001. These were the last critical tests in the UK horses; the entire herd was terminated in 2005. Population B small strongyles were established in horses on a pasture at the UK research farm on Old Lot 4 in 1966, and a satellite of this group was relocated to Field 24 in 1987. The last treatment of any of the horses in clinical tests on pasture was 22 years for Old Lot 4 (mostly benzimidazoles) and 5 years for Field 24 (TBZ) before the last critical test in 2001. Antiparasitic compounds (all paste formulations) administered orally in critical tests (n = 36) reported in this paper were TBZ (@ 44 mg/kg), pyrantel pamoate (PRT @ 6.6 mg base/kg), PTZ (@ 55 mg/kg), fenbendazole (FBZ @ 5 mg/kg), oxfendazole (OFZ @ 10 mg/kg), and oxibendazole (OBZ @ 10 mg/kg). The drug given and number of horses treated from Old Lot 4 were TBZ (18), PRT (3), PTZ (2), FBZ (2), OFZ (1), and OBZ (1) and from Field 24 were OFZ (1) and TBZ (8). Removal of small strongyles in Old Lot 4 was excellent for PRT, OFZ, and OBZ but much less for TBZ, PTZ, and FBZ. For the 16 species present in this lot, removal by TBZ was lowest for seven species (Coronocyclus (Cor.) coronatus, Cyathostomum (Cya.) catinatum, Cylicocyclus (Cyc.) nassatus, Cylicostephanus (Cys.) calicatus, Cylicostephanus goldi, Cylicostephanus longibursatus, and Cylicostephanus minutus). Of these seven species, lowest activity was found for five by PTZ and FBZ. One of the five resistant species was different for each of these two drugs. In Field 24, efficacy against small strongyles was excellent for the one foal treated with OFZ early (1992) in the study. TBZ initially had higher activity than in later years. Of the 12 small strongyle species present in this field, TBZ activity throughout the study was, in general, low for Cor. coronatus, Cys. goldi, and Cys. longibursatus, but it declined more or less progressively for Cya. catinatum, Cylicocyclus leptostomus, Cyc. nassatus, and Cys. calicatus over the study period. Cys. minutus were not present in high enough numbers to evaluate drug efficacy. Overall activity of TBZ on the group of small strongyles did not change; that is, susceptibility did not increase over time in Old Lot 4 where these parasites were not exposed to a benzimidazole for many years. However, in Field 24, where additional TBZ pressure was put on these parasites, efficacy not only did not increase but it decreased. From the data for small strongyles in the two groups of foals, eight species were considered benzimidazole resistant in varying degrees (most research on TBZ). Data on prevalence and drug activity on other internal parasite species besides small strongyles also are given.
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