Top Suppliers:I want be here

74226-22-5

74226-22-5 structure
74226-22-5 structure
  • Name: Dazoxiben
  • Chemical Name: 4-(2-imidazol-1-ylethoxy)benzoic acid,hydrochloride
  • CAS Number: 74226-22-5
  • Molecular Formula: C12H13ClN2O3
  • Molecular Weight: 268.69600
  • Catalog: Signaling Pathways GPCR/G Protein Prostaglandin Receptor
  • Create Date: 2017-03-05 08:47:46
  • Modify Date: 2024-01-10 16:53:35
  • Dazoxiben is a potent and orally active thromboxane (TX) synthase inhibitor[1].

Name 4-(2-imidazol-1-ylethoxy)benzoic acid,hydrochloride
Synonyms Dazoxiben hydrochloride
Dazoxiben HCl
Description Dazoxiben is a potent and orally active thromboxane (TX) synthase inhibitor[1].
Related Catalog
Target

Thromboxane (TX) synthase[1]

In Vitro Dazoxiben inhibits TXB2 production in clotting human whole blood with an IC50 of 0.3 μM and causes parallel enhancement of PGE2 greater than PGF2 alpha greater than 6-keto-PGF1 alpha production[1]. Dazoxiben inhibits TXB2 production in rat kidney glomeruli with an IC50 of 1.60 μM) than in rat whole blood (IC50= 0.32μM), and is not associated with changes in PGE2, PGF2 alpha and 6-keto-PGF1 alpha production[1].
In Vivo Dazoxiben (intraperitoneal administration; 100 μg/kg) produces a marked prolongation of the tail bleeding time with 96.8 ± 10.8 secs[2].
References

[1]. Patrignani P, et al. Differential effects of dazoxiben, a selective thromboxane-synthase inhibitor, on platelet and renal prostaglandin-endoperoxide metabolism.J Pharmacol Exp Ther. 1984 Feb;228(2):472-7.

[2]. Yu SM, et al. Pharmacological characterization of cinnamophilin, a novel dual inhibitor of thromboxane synthase and thromboxane A2 receptor.Br J Pharmacol. 1994 Mar;111(3):906-12.

Boiling Point 491.2ºC at 760 mmHg
Molecular Formula C12H13ClN2O3
Molecular Weight 268.69600
Flash Point 250.9ºC
Exact Mass 268.06100
PSA 64.35000
LogP 2.46230
Hazard Codes Xi

~79%

74226-22-5 structure

74226-22-5

Literature: Ono Pharmaceutical Co., Ltd. Patent: US4461905 A1, 1984 ;

~84%

74226-22-5 structure

74226-22-5

Literature: Cross, Peter E.; Dickinson, Roger P.; Parry, M. John; Randall, Michael J. Journal of Medicinal Chemistry, 1985 , vol. 28, # 10 p. 1427 - 1432

~%

74226-22-5 structure

74226-22-5

Literature: Cross, Peter E.; Dickinson, Roger P.; Parry, M. John; Randall, Michael J. Journal of Medicinal Chemistry, 1985 , vol. 28, # 10 p. 1427 - 1432

~%

74226-22-5 structure

74226-22-5

Literature: Biagi; Dell'Omodarme; Ferretti; Giorgi; Livi; Scartoni Farmaco, 1990 , vol. 45, # 11 p. 1181 - 1192