FenbendazoleFor pinworm treatment in animals CAS# 43210-67-9 |
- Elastase Inhibitor
Catalog No.:BCC1225
CAS No.:111682-13-4
- Elastase Inhibitor, SPCK
Catalog No.:BCC1226
CAS No.:65144-34-5
- α,β-Methyleneadenosine 5'-triphosphate trisodium salt
Catalog No.:BCC3591
CAS No.:7292-42-4
Quality Control & MSDS
Number of papers citing our products
Chemical structure
3D structure
| Cas No. | 43210-67-9 | SDF | Download SDF |
| PubChem ID | 3334 | Appearance | Powder |
| Formula | C15H13N3O2S | M.Wt | 299.35 |
| Type of Compound | N/A | Storage | Desiccate at -20°C |
| Solubility | DMSO : 10 mg/mL (33.41 mM; Need ultrasonic) H2O : < 0.1 mg/mL (insoluble) | ||
| Chemical Name | methyl N-(6-phenylsulfanyl-1H-benzimidazol-2-yl)carbamate | ||
| SMILES | COC(=O)NC1=NC2=C(N1)C=C(C=C2)SC3=CC=CC=C3 | ||
| Standard InChIKey | HDDSHPAODJUKPD-UHFFFAOYSA-N | ||
| Standard InChI | InChI=1S/C15H13N3O2S/c1-20-15(19)18-14-16-12-8-7-11(9-13(12)17-14)21-10-5-3-2-4-6-10/h2-9H,1H3,(H2,16,17,18,19) | ||
| General tips | For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months. We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months. Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it. |
||
| About Packaging | 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial. 2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial. 3. Try to avoid loss or contamination during the experiment. |
||
| Shipping Condition | Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request. | ||
| Description | Fenbendazole is a broad spectrum benzimidazole anthelmintic used against gastrointestinal parasites.
Target: Antiparasitic
Fenbendazole is a broad spectrum benzimidazole anthelmintic used against gastrointestinal parasites including: giardia, roundworms, hookworms, whipworms, the taenia species of tapeworms(It is effective against the Taenia species of tapeworm but not against the common tapeworm, Dipylidium caninum.), pinworms, aelurostrongylus, paragonimiasis, strongyles and strongyloides and can be administered to sheep, cattle, horses, fish, dogs, cats, rabbits and seals. Drug interactions may occur if using bromsalan flukicides such as dibromsalan and tribromsalan. Abortions in cattle and death in sheep have been reported after using these medications together. Fenbendazole is poorly absorbed from the gastrointestinal tract in most species. The LD50 in laboratory animals exceeds 10 g/kg when administered orally. From Wikipedia. References: | |||||
Fenbendazole Dilution Calculator
Fenbendazole Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 3.3406 mL | 16.7029 mL | 33.4057 mL | 66.8114 mL | 83.5143 mL |
| 5 mM | 0.6681 mL | 3.3406 mL | 6.6811 mL | 13.3623 mL | 16.7029 mL |
| 10 mM | 0.3341 mL | 1.6703 mL | 3.3406 mL | 6.6811 mL | 8.3514 mL |
| 50 mM | 0.0668 mL | 0.3341 mL | 0.6681 mL | 1.3362 mL | 1.6703 mL |
| 100 mM | 0.0334 mL | 0.167 mL | 0.3341 mL | 0.6681 mL | 0.8351 mL |
| * Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations. | |||||
Calcutta University
University of Minnesota
University of Maryland School of Medicine
University of Illinois at Chicago
The Ohio State University
University of Zurich
Harvard University
Colorado State University
Auburn University
Yale University
Worcester Polytechnic Institute
Washington State University
Stanford University
University of Leipzig
Universidade da Beira Interior
The Institute of Cancer Research
Heidelberg University
University of Amsterdam
University of Auckland
TsingHua University
The University of Michigan
Miami University
DRURY University
Jilin University
Fudan University
Wuhan University
Sun Yat-sen University
Universite de Paris
Deemed University
Auckland University
The University of Tokyo
Korea University
An anthelmintic drug belonging to the benzimidazole group mainly used for the treatment of pinworm in animals. Recently, fenbendazole has been shown to selectively induce cytotoxicity in cancer cells via impairment of proteasomal function and induction of unfolded protein response.
- Skp2 Inhibitor C1
Catalog No.:BCC6298
CAS No.:432001-69-9
- 6-(5-Chloropyridin-2-yl)-7-hydroxy-6,7-dihydro-5H-pyrrolo[3,4-b]pyrazin-5-one
Catalog No.:BCC8753
CAS No.:43200-81-3
- Zopiclone
Catalog No.:BCC9195
CAS No.:43200-80-2
- Allylestrenol
Catalog No.:BCC8814
CAS No.:432-60-0
- SJ 172550
Catalog No.:BCC2416
CAS No.:431979-47-4
- 7'-O-Ethylmarmin
Catalog No.:BCC8274
CAS No.:
- Necrostatin-1
Catalog No.:BCC2247
CAS No.:4311-88-0
- DPO-1
Catalog No.:BCC7398
CAS No.:43077-30-1
- Umckalin
Catalog No.:BCC9211
CAS No.:43053-62-9
- Deoxyshikonin
Catalog No.:BCN3006
CAS No.:43043-74-9
- Vinpocetine
Catalog No.:BCN2609
CAS No.:42971-09-5
- Cathepsin G Inhibitor I
Catalog No.:BCC3598
CAS No.:429676-93-7
- Formoterol Hemifumarate
Catalog No.:BCC4349
CAS No.:43229-80-7
- 6-Hydroxykaempferol
Catalog No.:BCN3334
CAS No.:4324-55-4
- Boc-Tyr-OMe
Catalog No.:BCC3459
CAS No.:4326-36-7
- Toddaculine
Catalog No.:BCN3639
CAS No.:4335-12-0
- 3-O-Acetyloleanolic acid
Catalog No.:BCN5486
CAS No.:4339-72-4
- VU 0357121
Catalog No.:BCC4595
CAS No.:433967-28-3
- Ethisterone
Catalog No.:BCC4478
CAS No.:434-03-7
- Methenolone acetate
Catalog No.:BCC9028
CAS No.:434-05-9
- Oxymetholone
Catalog No.:BCC4692
CAS No.:434-07-1
- Lithocholic Acid
Catalog No.:BCC3805
CAS No.:434-13-9
- Nandrolone
Catalog No.:BCC9086
CAS No.:434-22-0
- Dacarbazine
Catalog No.:BCC1174
CAS No.:4342-03-4
Effect of fenbendazole in water on pigs infected with Ascaris suum in finishing pigs under field conditions.[Pubmed:28285891]
Vet Parasitol. 2017 Apr 15;237:1-7.
The husbandry of pigs for meat production is a constantly developing industry. Most studies on the effects of Ascaris suum infection in pigs and its prevention with anthelmintics are over a decade old. We examined the effect of 2.5mg Fenbendazole per kg bodyweight administered in drinking water for two consecutive days on A. suum infection 1 and 6 weeks after pigs arrived to fattening units. We hypothesised that the treatment would reduce the presence of A. suum-infections, improve the average daily weight gain of pigs, reduce the percentage of liver rejections in pens by 50% and increase the lean meat percentage at slaughter by 1%. The study included a placebo group (427 pigs) and a treatment group (420 pigs) spanning four different farms previously reporting >/=15% liver rejection. The treatment was given for 2 consecutive days 1 and 6 weeks after the pigs arrived to the fattening unit. Faecal samples were collected during weeks 1, 6 and 12 from all pigs and examined for A. suum eggs. Blood was collected during weeks 1 and 12 from a subgroup of the pigs and examined for anti-A. suum antibodies and clinical blood parameters. Data on liver rejection and lean meat percentage were collected post-mortem. The proportion of Ascaris seropositive pigs changed from 8.6% to 22.2% and 20.3% to 16.3% in the placebo and treatment group respectively. Fenbendazole reduced the presence of A. suum eggs in faeces the percentage of liver rejections by 69.8%. The treatment did not affect daily weight gain or lean meat percentage. Pigs with A. suum eggs in faeces at week 6 had a lower average daily weight gain of 61.8g/day compared with pigs without parasite eggs. Fenbendazole treatment may be a useful option for farms struggling with persistent A. suum problems and demonstrate a beneficial effect on the weight gain of the animals shedding eggs in faeces and result in fewer condemned livers at slaughter.
In vitro anti-tubulin effects of mebendazole and fenbendazole on canine glioma cells.[Pubmed:28078780]
Vet Comp Oncol. 2017 Dec;15(4):1445-1454.
Benzimidazole anthelmintics have reported anti-neoplastic effects both in vitro and in vivo. The purpose of this study was to evaluate the in vitro chemosensitivity of three canine glioma cell lines to mebendazole and Fenbendazole. The mean inhibitory concentration (IC50 ) (+/-SD) obtained from performing the MTT [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] assay after treating J3T, G06-A, and SDT-3G cells for 72 h with mebendazole were 0.030 +/- 0.003, 0.080 +/- 0.015 and 0.030 +/- 0.006 muM respectively, while those for Fenbendazole were 0.550 +/- 0.015, 1.530 +/- 0.159 and 0.690 +/- 0.095 muM; treatment of primary canine fibroblasts for 72 h at IC50 showed no significant effect. Immunofluorescence studies showed disruption of tubulin after treatment. Mebendazole and Fenbendazole are cytotoxic in canine glioma cell lines in vitro and may be good candidates for treatment of canine gliomas. Further in vivo studies are required.
Anthelmintic Resistance of Strongyle Nematodes to Ivermectin and Fenbendazole on Cart Horses in Gondar, Northwest Ethiopia.[Pubmed:28265572]
Biomed Res Int. 2017;2017:5163968.
A study was conducted from November 2015 to April 2016 to determine Fenbendazole and ivermectin resistance status of intestinal nematodes of cart horses in Gondar, Northwest Ethiopia. Forty-five strongyle infected animals were used for this study. The animals were randomly allocated into three groups (15 horses per group). Group I was treated with Fenbendazole and Group II with ivermectin and Group III was left untreated. Faecal samples were collected from each cart horse before and after treatment. Accordingly, the reduction in the mean fecal egg count at fourteen days of treatment for ivermectin and Fenbendazole was 97.25% and 79.4%, respectively. It was significantly different in net egg count between treatment and control groups after treatment. From the study, resistance level was determined for Fenbendazole and suspected for ivermectin. In addition, a questionnaire survey was also conducted on 90 selected cart owners to assess their perception on anthelmintics. In the survey, the most available drugs in the study area used by the owners were Fenbendazole and ivermectin. Most respondents have no knowledge about drug management techniques. Hence, animal health extension services to create awareness regarding anthelmintic management that plays a key role in reducing the anthelmintic resistance parasites.
Mixture toxicity of flubendazole and fenbendazole to Daphnia magna.[Pubmed:28214179]
Int J Hyg Environ Health. 2017 May;220(3):575-582.
Nowadays, residual amounts of many pharmaceuticals can be found in various environmental compartments including surface and ground waters, soils and sediments as well as biota. Even though they undergo degradability, their environmental discharge is relatively continuous, thus they may be regarded as quasi-persistent contaminants, and are also frequently regarded as emerging organic pollutants. Benzimidazoles, especially flubendazole (FLU) and Fenbendazole (FEN), represent two anthelmintic drugs belonging to this group. Although their presence in environmental matrices has been reported, there is relatively little data concerning their (eco)toxicological impact. Furthermore, no data is available on their mixture toxicity. FLU and FEN have been found to have a strong impact on an environmentally important non-target organism - Daphnia magna. Moreover, these compounds are usually present in the environment as a part of pharmaceutical mixtures. Therefore, there is a need to evaluate their mixture toxicity, which was the main aim of this study. Single substance toxicity tests were carried out in parallel with mixture studies of FLU and FEN, with the application of two well established concepts of Concentration Addition (CA) and Independent Action (IA). As a result, both models (CA and IA) were found to underestimate the toxicity of mixtures, however CA yielded more accurate predictions.
