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53716-50-0
  • 奧吩達(dá)唑

  • names:

    Oxfendazole

  • CAS號(hào):

    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
奧吩達(dá)唑
Oxfendazole(奧吩達(dá)唑,53716-50-0)常溫下為白色或類白色粉末,有輕微的特殊氣味,它可以破壞胃腸道蠕蟲上皮細(xì)胞的微管結(jié)構(gòu),抑制蟲體從腸道內(nèi)攝取葡萄糖。
貨品編碼 規(guī)格 純度 價(jià)格 (¥) 現(xiàn)價(jià)(¥) 特價(jià)(¥) 庫(kù)存描述 數(shù)量 總計(jì) (¥)
YZM000788-25g 25g 98% ¥ 415.00 ¥ 415.00 298 1-2days
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0.00
YZM000788-5g 5g 98% ¥ 152.00 ¥ 152.00 108 1-2days
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0.00
YZM000788-1g 1g 98% ¥ 98.00 ¥ 98.00 68 1-2days
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中文別名 奧吩達(dá)唑(Oxfendazole,53716-50-0)奧酚噠唑、奧芬噠唑、苯亞砜咪酯、苯硫氧咪唑,是苯硫咪唑的亞砜形態(tài)
英文別名 Oxfendazole(奧吩達(dá)唑,53716-50-0)
CAS號(hào) 53716-50-0
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
溶解度Solubility 生物體外In Vitro:DMSO溶解度50 mg/mL(158.55 mM;Need ultrasonic)H2O : 0.67 mg/mL(2.12 mM;Need ultrasonic)
性狀 固體粉末,Power
儲(chǔ)藏條件 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
奧吩達(dá)唑(Oxfendazole,53716-50-0)毒性:
生物 測(cè)試類型 路線 報(bào)告劑量(標(biāo)準(zhǔn)化劑量) 影響 參考
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.

奧吩達(dá)唑(Oxfendazole,53716-50-0)理性質(zhì):
物理屬性 單位 溫度(攝氏度) 資源
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(奧吩達(dá)唑,53716-50-0)實(shí)驗(yàn)注意事項(xiàng):
1.實(shí)驗(yàn)前需戴好防護(hù)眼鏡,穿戴防護(hù)服和口罩,佩戴手套,避免與皮膚接觸。
2.實(shí)驗(yàn)過(guò)程中如遇到有毒或者刺激性物質(zhì)及有害物質(zhì)產(chǎn)生,必要時(shí)實(shí)驗(yàn)操作需要手套箱內(nèi)完成以免對(duì)實(shí)驗(yàn)人員造成傷害
3.實(shí)驗(yàn)后產(chǎn)生的廢棄物需分類存儲(chǔ),并交于專業(yè)生物廢氣物處理公司處理,以免造成環(huán)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:奧吩達(dá)唑MSDS,奧吩達(dá)唑蒸汽壓,奧吩達(dá)唑合成,奧吩達(dá)唑標(biāo)準(zhǔn),奧吩達(dá)唑應(yīng)用,奧吩達(dá)唑合成,奧吩達(dá)唑沸點(diǎn),奧吩達(dá)唑閃點(diǎn),奧吩達(dá)唑用途,奧吩達(dá)唑溶解度,奧吩達(dá)唑價(jià)格,奧吩達(dá)唑作用,奧吩達(dá)唑結(jié)構(gòu)式,奧吩達(dá)唑用處,奧吩達(dá)唑毒理性質(zhì),奧吩達(dá)唑物理性質(zhì)
產(chǎn)品說(shuō)明 奧吩達(dá)唑(Oxfendazole,53716-50-0)屬于稱為苯并咪唑的有機(jī)化合物。 奧吩達(dá)唑含有與咪唑環(huán)稠合的苯環(huán)的有機(jī)化合物
IntroductionOxfendazole(奧吩達(dá)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
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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