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115103-15-6

115103-15-6 structure
115103-15-6 structure
  • Name: tribendimidine
  • Chemical Name: N'-[4-[[4-[[4-[1-(dimethylamino)ethylideneamino]phenyl]iminomethyl]phenyl]methylideneamino]phenyl]-N,N-dimethylethanimidamide
  • CAS Number: 115103-15-6
  • Molecular Formula: C28H32N6
  • Molecular Weight: 452.59400
  • Catalog: Chemical reagent Organic reagent Imine, hydrazine
  • Create Date: 2018-06-18 18:58:23
  • Modify Date: 2024-01-11 20:29:24
  • Tribendimidine is an orally active, broad-spectrum anthelmintic agent, with particularly high activity against A. lumbricoides and N. americanus. Tribendimidine is also an L-type nicotinic acetylcholine receptor (nAChR) agonist[1][2][3].

Name N'-[4-[[4-[[4-[1-(dimethylamino)ethylideneamino]phenyl]iminomethyl]phenyl]methylideneamino]phenyl]-N,N-dimethylethanimidamide
Synonyms Tribendimidine
Tribendimidin
Description Tribendimidine is an orally active, broad-spectrum anthelmintic agent, with particularly high activity against A. lumbricoides and N. americanus. Tribendimidine is also an L-type nicotinic acetylcholine receptor (nAChR) agonist[1][2][3].
Related Catalog
In Vitro Tribendimidine (100 μg/mL, 24 h) shows intoxication of C. elegans[3]. Tribendimidine (0-100 μg/mL, 6 days) shows toxicity with an LC50 value (concentration at which half the animals are dead) of 54.4 μg/mL[3]. Tribendimidine (0-200 μg/mL, 64 h)-induced sterility is resisted by trb mutant hermaphrodites, and Levamisole-resistant mutants are resistant to Tribendimidine. [3].
In Vivo Tribendimidine (75 and 150 mg/kg; p.o.; once) shows inhibition activity against C. sinensis in rats, and shows inhibition against O. viverrini at 400 mg/kg in hamsters[2]. Animal Model: C. sinensis infected Female Wistar rats[2] Dosage: 75 mg/kg and 150 mg/kg Administration: Oral administration, once Result: A 99.1% worm burden reduction was achieved at 150 mg/kg, and the worm burden reduction was still significant (68.9%) at 75 mg/kg.
References

[1]. Xiao SH, et al. Tribendimidine: a promising, safe and broad-spectrum anthelmintic agent from China. Acta Trop. 2005 Apr;94(1):1-14.

[2]. Keiser J, et al. Evaluation of the in vivo activity of tribendimidine against Schistosoma mansoni, Fasciola hepatica, Clonorchis sinensis, and Opisthorchis viverrini. Antimicrob Agents Chemother. 2007 Mar;51(3):1096-8.

[3]. Hu Y, et al. The new anthelmintic tribendimidine is an L-type (levamisole and pyrantel) nicotinic acetylcholine receptor agonist. PLoS Negl Trop Dis. 2009 Aug 11;3(8):e499.

Density 1.04g/cm3
Boiling Point 618.2ºC at 760mmHg
Molecular Formula C28H32N6
Molecular Weight 452.59400
Flash Point 327.7ºC
Exact Mass 452.26900
PSA 55.92000
LogP 6.41080
Vapour Pressure 3.26E-15mmHg at 25°C
Index of Refraction 1.575
Storage condition 2-8°C