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Merck
CN

O3132

奥苯达唑

~98%

别名:

(5-丙氧基-1H-苯并咪唑-2-基)氨基甲酸甲酯

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关于此项目

经验公式(希尔记法):
C12H15N3O3
化学文摘社编号:
分子量:
249.27
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
243-877-7
MDL number:
Assay:
~98%
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InChI key

RAOCRURYZCVHMG-UHFFFAOYSA-N

InChI

1S/C12H15N3O3/c1-3-6-18-8-4-5-9-10(7-8)14-11(13-9)15-12(16)17-2/h4-5,7H,3,6H2,1-2H3,(H2,13,14,15,16)

SMILES string

CCCOc1ccc2[nH]c(NC(=O)OC)nc2c1

assay

~98%

storage temp.

2-8°C

Quality Level

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Biochem/physiol Actions

驱肠虫剂

存储类别

11 - Combustible Solids

wgk

WGK 3

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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G W Lubega et al.
Biochemical pharmacology, 41(1), 93-101 (1991-01-01)
The low- and high-affinity binding of tritiated benzimidazole anthelmintics (mebendazole and oxibendazole) to tubulin-containing supernatants derived from unembryonated eggs, third stage larvae or adult worms of thiabendazole-susceptible and -resistant strains of Haemonchus contortus were examined and compared. The displacement of
A field evaluation of three methods of administration of anthelminthics to horses.
C Uhlinger et al.
Equine veterinary journal, 24(6), 487-488 (1992-11-01)
S C Tolliver et al.
American journal of veterinary research, 54(6), 908-913 (1993-06-01)
Critical tests were conducted in horses (n = 11) with naturally acquired infections of benzimidazole (BZ)-resistant population-B small strongyles in 1989 and 1990. Anthelmintics administered were thiabendazole (44 mg/kg of body weight, n = 4), oxibendazole (10 mg/kg, n =
M R Chapman et al.
Veterinary parasitology, 66(3-4), 205-212 (1996-11-15)
Three fecal egg count reduction assays (FECR) and one critical trial were performed to determine the efficacy of pyrantel pamoate (PP) at 6.6 mg base kg-1 on a well managed stud farm in Louisiana where a loss of efficacy was
S E Bunch
The Veterinary clinics of North America. Small animal practice, 23(3), 659-670 (1993-05-01)
Historical aspects, mechanisms, and treatment of hepatotoxicity associated with pharmacologic agents in dogs and cats are discussed. All agents that cause clinically relevant drug-induced hepatotoxicity have been reviewed within the last 5 years; therefore, only selected drugs that more recently

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